Tesi sul tema "Th2"
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1
Podgaec, Sérgio. "Padrões de resposta imune em pacientes com endometriose". Universidade de São Paulo, 2006. http://www.teses.usp.br/teses/disponiveis/5/5139/tde-31102006-105026/.
Testo completoAbstract (sommario):
Objetivo: O objetivo deste estudo foi analisar a relação e a predominância dos padrões de resposta imune Th1 e Th2 em pacientes com endometriose. Pacientes e Métodos: Entre Fevereiro de 2004 e Abril de 2005 foram avaliadas 98 pacientes divididas em dois grupos de acordo com a presença (Grupo A) ou ausência de endometriose (Grupo B), confirmada histologicamente. Foram coletados sangue periférico e fluido peritoneal de todas as pacientes para a dosagem de interleucinas (IL) 2, 4 e 10, fator de necrose tumoral-alfa (TNF-alfa) e interferon-gama (IFN-gama) por citometria de fluxo. Além da presença da endometriose, foram analisadas a fase do ciclo menstrual, o quadro clinico, o estadiamento, o local de acometimento e a classificação histológica da moléstia. Resultados: Observou-se elevação estatisticamente significante nas concentrações de IFN-gama (mediana de 1,5pg/ml no Grupo A e de 0,4pg/ml no Grupo B, p=0,03) e de IL-10 (mediana de 38,6pg/ml no Grupo A e de 15,7pg/ml no Grupo B, p=0,03) do fluido peritoneal das pacientes com endometriose em relação àquelas sem a doença. As pacientes com endometriose apresentaram alteração estatisticamente significativa na relação das concentrações de IL-4/IFN-gama (p<0,001), IL-4/IL-2 (p=0,006), IL-10/IFN-gama (p < 0,001) e IL-10/IL-2 (p<0,001) do fluido peritoneal, com concentrações mais elevadas da IL-4 e da IL-10, o que reflete o predomínio da resposta Th2 sobre a Th1. Conclusão: Os resultados obtidos permitem concluir que, neste estudo, observou-se elevação de citocinas relativas à resposta imune Th2, denotando haver um predomínio deste padrão de resposta em pacientes com endometriose.Objective: The objective of this study was to analyze the relation and the predominance of the immune response patterns Th1 and Th2 in patients with endometriosis. Patients and Methods: Between February 2004 and April 2005, 98 patients were evaluated and divided into two groups, according to the presence (Group A) or absence of endometriosis (Group B), confirmed by histology. Peripheral blood and peritoneal fluid were collected from all patients to obtain the concentrations of interleukines (IL) 2, 4 and 10, tumor necrosis factor-alpha (TNF-alpha) and interferon-gamma (IFN-gamma) using flow cytometry. Besides the presence of endometriosis, we analyzed phase of menstrual cycle, clinical complaints, classification, site and histological differentiation of the disease. Results: We observed higher concentrations of IFN-gamma (median of 1.5pg/ml in Group A and 0.4pg/ml in Group B, p = 0.03) and IL-10 (median of 38.6pg/ml in Group A and 15.7pg/ml in Group B, p = 0.03) in peritoneal fluid of patients with endometriosis in relation to those without the disease. Patients with endometriosis presented a significant alteration in IL-4/IFN-gamma (p < 0.001), IL-4/IL-2 (p = 0.006), IL-10/IFN-gamma (p < 0.001) and IL-10/IL-2 (p<0.001) ratio concentrations of peritoneal fluid, with IL-4 and IL-10 predominance, reflecting a Th2 response predominance over the Th1. Conclusion: The results allow concluding that, in this study, it was observed a cytokine elevation related to Th2 immune response, indicating a predominance of this pattern of response in patients with endometriosis.
2
Strzelczyk, Barbara. "Cytokin mRNA profil i perifera mononukleära celler hos barn med födoämnesallergi". Thesis, Umeå universitet, Biomedicinsk laboratorievetenskap, 2011. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-58649.
Testo completo
3
Rao, Venkata Lakshmi Prakruthi. "Epigenetic Reprogramming at the Th2 Locus". University of Cincinnati / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1543838686940608.
Testo completo
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Ahyi, Ayélé-Nati. "The role of PU.1 and IRF4 interaction in the biology and function of T helper 2 cells". Connect to resource online, 2009. http://hdl.handle.net/1805/1882.
Testo completoAbstract (sommario):
Thesis (Ph.D.)--Indiana University, 2009.Title from screen (viewed on August 26, 2009). Department of Microbiology and Immunology, Indiana University-Purdue University Indianapolis (IUPUI). Advisor(s): Mark Kaplan. Includes vita. Includes bibliographical references (leaves 107-125).
5
Costa, Fernando Augusto Miranda da. "Resposta imune in vitro aos antígenos de Papilomavírus Humano (HPV) em homens na cidade de São Paulo, Brasil". Universidade de São Paulo, 2013. http://www.teses.usp.br/teses/disponiveis/5/5133/tde-04022014-155625/.
Testo completoAbstract (sommario):
Introdução: O Papilomavírus Humano está muito bem associado com diversos tipos de cânceres humanos, como câncer anogenital e oral. Alguns estudos demonstram que o aparecimento de lesões e a progressão para o câncer estão relacionados ao tipo de resposta imune do hospedeiro. Deste modo, evidências indicam que a resposta imune do hospedeiro tem um papel muito importante para o curso da infecção pelo HPV. Objetivo: Avaliar a resposta imune específica in vitro ao Papilomavírus Humano (HPV) em homens com lesões causadas por HPV e sem lesão por HPV. Material e Métodos: Foram recrutados 31 pacientes e 11 voluntários, que formaram 4 grupos de estudo; sendo 12 pacientes no Grupo A (HIV +/ HPV +); 09 pacientes no Grupo B (HIV-/HPV+); 10 pacientes no Grupo C (HIV+/ HPV-); e 11 indivíduos saudáveis no Grupo D (HIV-/HPV-). Foram realizados ensaios de cultura celular para mensurar a resposta celular específica \"in vitro\" do tipo Th1/Th2/Th17 (INF-y, IL-2, TNFalfa, IL-4, IL-10 e IL-17) sob o estímulo da vacina quadrivalente do HPV (HPV 6, 11, 16 e 18) e à proteína E7 de HPV-16. Resultados: O grupo coinfectado (HIV +/ HPV+) apresentou níveis mais elevados de citocinas, principalmente do perfil Th2, comparando-se com os dados dos demais grupos de estudo. O grupo coinfectado apresentou níveis elevados de IL-6 e IL-10 (Perfil Th2) em relação ao grupo controle (HIV-/HPV-), com significância estatística (p < 0.0001 e p < 0.0001, respectivamente). Conclusão: Foi demonstrada uma elevada produção de citocinas no grupo HPV+/HIV+, sugerindo uma forte imunomodulação pela coinfecção HIV/HPV. Entretanto, novos estudos devem ser realizados para comprovar estes dados. Além de apresentar um perfil essencialmente Th2 do grupo coinfectado, principalmente pelos níveis elevados de IL-6 e IL-10 apresentados, sugerindo que estas duas citocinas possam servir como biomarcadores para persistência viral, uma vez que, os pacientes soropositivos para HIV apresentam maior persistência de HPV, e monitorar a progressão para lesões mais gravesIntroduction: Human Papillomavirus is associated with different types of human cancers, such as anogenital and oral cancer. Some studies show that the appearance of lesions and progression to cancer are related to the type of host immune response. Thus, evidence indicates that the host immune response has a role key in the course of HPV infection. Objective: To evaluate the specific immune response in vitro to HPV in men with lesions caused by HPV and without injury caused by HPV. Methods: We recruited 31 patients and 11 volunteers, who formed four groups, with 12 patients in Group A (HIV+/HPV+); 09 patients in Group B (HIV-/HPV+); 10 patients in Group C (HIV+/HPV-) and 11 healthy subjects in Group D (HIV-/HPV-). Cells culture assay was performed to measure the specific immune response \"in vitro\" Th1/Th2/Th17 (IFN-y, IL-2, TNF-alfa, IL-4, IL-10 and IL-17) under the stimulation of quadrivalent HPV vaccine (HPV 6, 11, 16 and 18) and the E7 protein of HPV-16. Results: The coinfected group (HIV+/HPV+) had higher levels of cytokines, especially Th2 profile, compared with data from the other study groups. The coinfected group showed high levels of IL-6 and IL-10 (Th2 profile) compared to the control Group (HIV- /HPV-), with statistical significance (p < 0.0001 and p < 0.0001, respectively). Conclusion: This study demonstrated a high production of cytokines in the coinfected group, suggesting a strong immunomodulation by coinfection HIV/HPV. However, further studies should be conducted to confirm these data. In addition to presenting essentially a Th2 profile, especially by high levels of IL-6 and IL-10 presented, suggesting that these two cytokines may serve as biomarkers for viral persistence, since HIV seropositive patients have a higher persistence of HPV, and monitor the progression to more serious injuries
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Persson, Marie, Christina Ekerfelt, Jan Ernerudh, Leif Matthiesen, Martina Sandberg, Yvonne Jonsson, Göran Berg e Maria C. Jenmalm. "Reduced IFN-γ and IL-10 responses to paternal antigens during and after pregnancy in allergic women". Linköpings universitet, Institutionen för klinisk och experimentell medicin, 2012. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-84900.
Testo completoAbstract (sommario):
Normal pregnancy and allergy are both characterized by a T helper (Th) 2 deviation. In the current study, we hypothesized that paternal antigen-induced cytokine responses during pregnancy would be deviated toward Th2 and an anti-inflammatory profile, and that the Th2 deviation would be more pronounced in allergic pregnant women. Blood samples were collected longitudinally on three occasions during pregnancy and two occasions post partum (pp). Of the 86 women initially included, 54 women had a normal pregnancy and completed the sampling procedures. Twelve women fulfilled the criteria for allergy (allergic symptoms and circulating immunoglobulin [Ig] E antibodies to inhalant allergens) and 20 were non-allergic (nonsensitized without symptoms). The levels of Th1- and Th2-associated cytokines and chemokines, the Th17 cytokine IL-17 and the anti-inflammatory cytokine IL-10 of the groups were compared. Paternal antigen-induced IL-4 and IL-10 responses increased between the first and the third trimester. Allergy was associated with decreased paternal antigen-induced IFN-γ and CXCL10 secretion in the nonpregnant state (one year pp) and also decreased IFN-γ/IL-4 and IFN-γ/IL-13 ratios during pregnancy. We also observed a decreased paternal antigen-induced IL-10 response in allergic compared with non-allergic women during pregnancy, along with a decreased IL-10/IL-13 ratio. In conclusion, our findings support the hypothesis of lower Th1 responses toward paternal antigens in allergic than in non-allergic women, but also indicate that allergy is associated with a lower capacity to induce anti-inflammatory IL-10 responses after paternal antigen stimulation during pregnancy.Funding Agencies|Swedish Research Council||Cancer and Allergy Association||Olle Engkvist Foundation||Vardal Foundation for Health Care Sciences and Allergy Research||National Swedish Association against Allergic Diseases||Linkoping University Hospital||
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Chiang, Sonnig Sue Whei. "Th1/Th2 imbalance in schizophrenia". Diss., lmu, 2005. http://nbn-resolving.de/urn:nbn:de:bvb:19-35074.
Testo completo
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Zhang, Ping. "The selective effect of dietary n-3 polyunsaturated fatty acids on murine Th1 and Th2 cell development". Diss., Texas A&M University, 2005. http://hdl.handle.net/1969.1/4148.
Testo completoAbstract (sommario):
To examine how dietary n-3 polyunsaturated fatty acids affect Th2 cell development, female C57BL/6 mice were fed a washout corn oil (CO) diet for 1 wk followed by 2 wk of either the same CO diet or a fish oil (FO) diet. CD4+ T cells were isolated from spleens and cultured under both neutral (anti-CD3 and phorbol myristate acetate (PMA)) and Th2 polarizing conditions (anti-CD3 and PMA, in presence of rIL-4, rIL-2, and anti-IFN-ó) in the presence of homologous mouse serum (HMS) or fetal bovine serum (FBS) for 2 d. Dietary n-3 PUFA significantly enhanced Th2 cell development and suppressed Th1 development under neutral conditions as assessed by intracellular cytokine staining for IL-4 and IFN-ó as the two prototypic Th2 and Th1 cytokines, respectively. However, under Th2 polarizing conditions, while the suppression of Th1 cells was maintained in FO-fed mice, no dietary effect was observed in Th2 cells. Dietary FO increased the Th2/Th1 ratio under both neutral and Th2 polarizing conditions with HMS in the cultures. To examine the effect of dietary n-3 PUFA on Th1 development, DO11.10 Rag2-/- mice expressing transgenic T cell receptor specific for ovalbumin (OVA) peptide were used. CD4+ T cells were isolated from spleens and lymph nodes and stimulated with ovalbumin (OVA) peptide and irradiated BALB/c splenocytes in the presence of rIL-12, anti-IL-4, and rIL-2 in HMS for 2d. Cells were expanded for another 3 d in the presence of rIL-2 and rIL-12. Dietary n-3 PUFA did not affect Th1 differentiation as assessed by the proportion of IFN-ó+, IL-4- T cells in the cultures, but suppressed rIL-2 induced expansion. The suppressed expansion was due to suppressed proliferation (p<0.05). In vivo expansion of antigen-specific T cells was visualized by flow cytometric analysis of CFSE-positive transgenic T cells. Dietary n-3 PUFA did not appear to affect antigen-induced CD4+ T cell cycle progression in vivo. Overall, these results suggest dietary n-3 PUFA have no direct effect on Th2 cell development but do directly suppress Th1 cell development following both mitogenic and antigenic stimulation in vitro.
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Gonçales, Juliana Prado. "Associação entre a infecção pelo trichuris trichiura, produção de citocinas e doenças alérgicas das vias respiratórias (asma) em crianças da Região Metropolitana do Recife, Pernambuco". Universidade Federal de Pernambuco, 2015. https://repositorio.ufpe.br/handle/123456789/16508.
Testo completoAbstract (sommario):
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CAPEs
A prevalência de doenças alérgicas, como rinite e asma, é menor em países subdesenvolvidos, onde há uma maior exposição a agentes infecciosos, como os helmintos. A relação entre infecções com T. trichiura e a prevalência das doenças alérgicas e reatividade cutânea ainda não está estabelecida. Os estudos divergem quanto à alteração (potencializar ou reduzir) do quadro clínico e/ou testes cutâneos, bem como, a carga parasitária da população estudada. O estudo teve como objetivo verificar se existe diferença entre a ocorrência de asma alérgica, prick test, níveis séricos das citocinas IL-4, IL-6, IL-10, TNF-α e anticorpos IgE anti-ascaris em crianças com infecção ativa por T. trichiura. Para isto, crianças com ou sem asma foram definidas pelo questionário ISAAC, foram realizados o prick-test, parasitológico (Hoffman/Kato Katz) e coleta de sangue, que foi submetido a cultura (estimulada com PHA) e o sobrenadante coletado para a dosagens das citocinas (CBA). A prevalência de crianças com parasitológico positivo foi de 16,9 % (61/361 crianças), entre essas 27,9 % (17/61) foram positivas para infecção por Trichuris trichiura (12/17) ou co-infectadas por Trichuris trichiura/ Ascaris lumbricoides (5/17). O grupo de pacientes infectados, com ou sem asma, produziram níveis significantemente elevados para todas as citocinas em relação ao grupo controle. Além disso, o grupo dos pacientes infectados sem asma apresentou um tendência maior de produção de IL-6, TNF-alfa e IL-10 que os com asma; os pacientes infectados e asmáticos apresentaram uma menor reatividade no Prick Test quando comprado aos asmáticos não infectados. Então, a infecção por T. trichiura parece modular positivamente os níveis das citocinas TNF-α, IL-10 e IL-6, mas em pacientes asmáticos estes níveis tendem a ser controlados. As reações de hipersensibilidade cutânea imediata parece ser menos frequente em asmáticos quando infectados. Os dados levantam a possibilidade de uma modulação mútua entre asma e tricuríase, favorecendo um estado de maior cronicidade de ambas entidades de doença.
The prevalence of allergic diseases such as rhinitis and asthma is smaller in developing countries, where there is a greater exposure to infectious agents, such as helminths. The relationship between infection with T. trichiura and the prevalence of allergic diseases and skin reactivity is not yet established. Studies differ as to the nature of the change (increase or reduce) in the clinical condition and/or skin tests, as well as the parasite load of the studied population. The study aimed to determine whether there are differences between the occurrence of allergic asthma, prick test, serum levels of IL-4, IL-6, IL-10, TNF-α and anti-Ascaris IgE antibodies in children with active infection by T. trichiura. For this purpose, children with and without asthma were defined by the ISAAC questionnaire, prick-test and parasitological (Hoffman/Kato Katz) were performed and blood samples were collected, which were then subjected to culture (stimulated with PHA) and the collected supernatant for cytokines measurements (CBA). The prevalence of children with positive parasitological was 16.9% (61/361 children), and among these 27.9% (17/61) were positive for Trichuris trichiura infection (12/17) or co-infected with Trichuris trichiura/Ascaris lumbricoides (5/17). The group of infected patients, with or without asthma, produced significantly high levels for all cytokines in the control group. Furthermore, the group of patients infected without asthma showed a greater tendency of IL-6,TNF-α and IL-10 production than those with asthma; infected and asthmatic patients had a lower reactivity in Prick Test when compared to those with asthma who were uninfected. Thus, the infection with T. trichiura positively modulates the levels of TNF-α, IL-10 and IL-6 cytokines, but these levels in asthmatic patients tend to be controlled. The immediate hypersensitivity skin reactions appears to be less common in asthmatics when infected. The data raise the possibility of a mutual modulation between asthma and trichuriasis, favoring a state of chronic course on both disease entities.
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Kazak, Ilkay. "Th1-Th2-Zytokine bei entzündlicher Herzmuskelerkrankung". [S.l.] : [s.n.], 2002. http://www.diss.fu-berlin.de/2002/70/index.html.
Testo completo
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Morelli, Fernando Christiano Gabriel [UNESP]. "Quantificação de citocinas no conteúdo abomasal de bovinos de corte na presença ou ausência de ulceração gástrica". Universidade Estadual Paulista (UNESP), 2016. http://hdl.handle.net/11449/134249.
Testo completoAbstract (sommario):
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Erosões e úlceras são achados comuns no abomaso e causam preocupação econômica nos mais variados sistemas de produção de gado. Muitos fatores podem predispor ao aparecimento de úlceras e acúmulo de gases no abomaso, incluindo alimentos grosseiros, estresse ambiental, deficiências de vitaminas e minerais e infecções bacterianas. Essas úlceras podem ser subclínicas, sendo descobertas nas necropsias ou após o abate do animal, ou levarem à redução da motilidade do órgão, prejudicando o fluxo do seu conteúdo e causando transtornos digestivos graves e até ao aparecimento de síndromes semelhantes à indigestão vagal. Existem informações a respeito da resposta do sistema imune na maior parte das mucosas do trato gastrintestinal de não-ruminantes e ruminantes, porém são raras a respeito do abomaso. Os objetivos desse estudo foram detectar os níveis de citocinas (IL-17A, IFN-γ, TNF-α, IL-10, IL-6, IL-4, IL-2) no conteúdo abomasal em bovinos de corte, determinar o perfil Th1 ou Th2 dessas citocinas em animais com úlceras de grau 1 e 2 na região cárdica abomasal e comparar esses valores com os níveis de citocinas de animais sem úlceras (controle), em amostras colhidas em abatedouro, para auxiliar na compreensão da fisiopatologia do processo inflamatório local. A avaliação macroscópica e a classificação das úlceras foi realizada por meio de exames visual e histológico em amostras de tecidos da parede da região cárdica abomasal ulcerada. Os níveis de citocinas produzidas do líquido abomasal dos animais com ou sem úlceras foram avaliados por citometria de fluxo (método Cytometric Bead Array). As citocinas citadas foram detectadas no líquido do abomaso dos bovinos. Não houve diferença na liberação das citocinas entre os grupos com úlceras e o grupo sem úlcera, indicando um equilíbrio entre perfis Th1 e Th2 da resposta inflamatória.
Erosions and ulcers are common findings in the abomasum and cause economic concern in several livestock production systems. Many factors may predispose to ulcers and bloat in the abomasum, including roughage, environmental stress, deficiencies of vitamins and minerals and bacterial infections. These ulcers may be subclinical and are found during necropsy or after slaughter, or lead to reduction of abomasal motility, hindering the flow of your content and causing serious digestive disorders and even the appearance of syndromes similar to vagal indigestion. There are some studies evaluating the immune system response in most of the mucous membranes of the gastrointestinal tract of non-ruminants and ruminants, but rarely related to the abomasum. The aims of this study were to investigate the levels of cytokines (IL-17A, IFN-γ, TNF-α, IL-10, IL-6, IL-4, IL-2) in the abomasal fluid of beef cattle, to determine the Th1 or Th2 profile of these cytokines in animals with types 1 or 2 ulcers located in the abomasal cardic region and to compare these levels with those of animals without ulcers (controls), in samples collected in an abbatoir, to help to the understand the pathophysiology of the local inflammatory process. Ulcers from the abomasal cardic region were macroscopicaly evaluated, then classified by histology. Cytokine levels in the abomasal fluid from animals with or without ulcers were evaluated by flow cytometry (Cytometric Bead Array). Cytokines were detected in the abomasum fluid of cattle. There was no difference in the release of cytokines between groups, indicating a balance between Th1 and Th2 profiles of the inflammatory response.
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Morelli, Fernando Christiano Gabriel. "Quantificação de citocinas no conteúdo abomasal de bovinos de corte na presença ou ausência de ulceração gástrica /". Araçatuba, 2016. http://hdl.handle.net/11449/134249.
Testo completoAbstract (sommario):
Orientador: Juliana Regina PeiróBanca: Lina Maria Wehrle Gomide
Banca:Fernanda Bovino
Banca: José Paes de Oliveira Filho
Banca:Glenda Nicioli da Silva
Resumo: Erosões e úlceras são achados comuns no abomaso e causam preocupação econômica nos mais variados sistemas de produção de gado. Muitos fatores podem predispor ao aparecimento de úlceras e acúmulo de gases no abomaso, incluindo alimentos grosseiros, estresse ambiental, deficiências de vitaminas e minerais e infecções bacterianas. Essas úlceras podem ser subclínicas, sendo descobertas nas necropsias ou após o abate do animal, ou levarem à redução da motilidade do órgão, prejudicando o fluxo do seu conteúdo e causando transtornos digestivos graves e até ao aparecimento de síndromes semelhantes à indigestão vagal. Existem informações a respeito da resposta do sistema imune na maior parte das mucosas do trato gastrintestinal de não-ruminantes e ruminantes, porém são raras a respeito do abomaso. Os objetivos desse estudo foram detectar os níveis de citocinas (IL-17A, IFN-γ, TNF-α, IL-10, IL-6, IL-4, IL-2) no conteúdo abomasal em bovinos de corte, determinar o perfil Th1 ou Th2 dessas citocinas em animais com úlceras de grau 1 e 2 na região cárdica abomasal e comparar esses valores com os níveis de citocinas de animais sem úlceras (controle), em amostras colhidas em abatedouro, para auxiliar na compreensão da fisiopatologia do processo inflamatório local. A avaliação macroscópica e a classificação das úlceras foi realizada por meio de exames visual e histológico em amostras de tecidos da parede da região cárdica abomasal ulcerada. Os níveis de citocinas produzidas do líquido abomasal... (Resumo completo, clicar acesso eletrônico abaixo)
Abstract: Erosions and ulcers are common findings in the abomasum and cause economic concern in several livestock production systems. Many factors may predispose to ulcers and bloat in the abomasum, including roughage, environmental stress, deficiencies of vitamins and minerals and bacterial infections. These ulcers may be subclinical and are found during necropsy or after slaughter, or lead to reduction of abomasal motility, hindering the flow of your content and causing serious digestive disorders and even the appearance of syndromes similar to vagal indigestion. There are some studies evaluating the immune system response in most of the mucous membranes of the gastrointestinal tract of non-ruminants and ruminants, but rarely related to the abomasum. The aims of this study were to investigate the levels of cytokines (IL-17A, IFN-γ, TNF-α, IL-10, IL-6, IL-4, IL-2) in the abomasal fluid of beef cattle, to determine the Th1 or Th2 profile of these cytokines in animals with types 1 or 2 ulcers located in the abomasal cardic region and to compare these levels with those of animals without ulcers (controls), in samples collected in an abbatoir, to help to the understand the pathophysiology of the local inflammatory process. Ulcers from the abomasal cardic region were macroscopicaly evaluated, then classified by histology. Cytokine levels in the abomasal fluid from animals with or without ulcers were evaluated by flow cytometry (Cytometric Bead Array). Cytokines were detected in the abomasu... (Complete abstract click electronic access below)
Doutor
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Persson, Marie, Christina Ekerfelt, Barbara Jablonowska, Yvonne Jonsson, Jan Ernerudh, Maria C. Jenmalm e Göran Berg. "Immunological status in patients undergoing in vitro fertilisation : responses to hormone treatment and relationship to outcome". Linköpings universitet, Institutionen för klinisk och experimentell medicin, 2012. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-85640.
Testo completoAbstract (sommario):
We aimed to prospectively investigate the paternal antigen-induced cytokine secretion by peripheral blood mononuclear cells (PBMCs) in response to hormone treatment in women undergoing in vitro fertilisation (IVF) and to examine the predictive value of the cytokine secretion profile in the outcome of IVF treatment, in a pilot study. Twenty-five women were included and IVF treatment was successful for six and unsuccessful for 19 women. Blood samples were collected before IVF treatment, on four occasions during IVF and four weeks after embryo transfer. The numbers of Th1-, Th2- and Th17-associated cytokine-secreting cells and cytokine levels in cell supernatants were analysed by enzyme-linked immunospot-forming (ELISpot), enzyme-linked immune-sorbent (ELISA) or Luminex assay. None of the cytokines (IFN-γ, IL-4, IL-5, IL-10, IL-12, IL-13, IL-17, TNF and GM-CSF) had any predictive value regarding IVF outcome. The majority of the cytokines reached their peak levels at ovum pick-up, suggesting an enhancing influence of the hormonal stimulation. Pregnancy was associated with a high number of IL-4-, IL-5- and IL-13-secreting cells four weeks after ET. In conclusion, the results do not support our hypothesis of a more pronounced peripheral Th1 and Th17 deviation towards paternal antigens in infertile women with an unsuccessful IVF outcome, although this is based on a small number of observations. A larger study is required to confirm this conclusion. Higher numbers of Th2-associated cytokine-secreting cells in pregnant women four weeks after ET do corroborate the hypothesis of a Th2 deviation during pregnancy.
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Lu, Thomas X. "MicroRNA in the Pathogenesis of Allergic Inflammation". University of Cincinnati / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1329935942.
Testo completo
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Pinto, Kerollen Runa, e 92994459263. "Expressão heteróloga da enteroquinase em enzima Escherichia coli". Universidade Federal do Amazonas, 2017. https://tede.ufam.edu.br/handle/tede/6783.
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FAPEAM - Fundação de Amparo à Pesquisa do Estado do Amazonas
Enterokinase (EC 3.4.21.9) is a heterodimer serine protease, a natural activator of trypsinogen, capable of cleaving specifically the sequence Asp-Asp-Asp-Asp-Lys. Due to the high specificity of the recognition site, it became a great tool of biotechnological interest. It is usually used to remove affinity tags in vitro, of recombinant proteins. In this work, the molecular cloning strategy resulted in the construction of the pDMK06, capable of programming the regulated expression of a heterologous gene ETK-Trx in E. coli. Through the cleavage process with restriction enzymes NdeI and BamHI, it was possible to obtain the coding sequence of the fusion protein between enterokinase and thioredoxin (ETK-Trx) of approximately 1259 bp from pENTK plasmid. Then, this sequence was subcloned at NdeI and BamHI sites of the expression vector pDM02, originating the recombinant plasmid pDMK06. This vector contains the TH2 promoter, which is efficiently regulated by Lac operator/repressor. E. coli JM110 cells transformed with the recombinant plasmid showed smaller growth in a solid medium when the expression of the heterologous protein was induced by IPTG in comparison with the control; however, this effect was not detected in the liquid medium. Furthermore, the E. coli cells morphology was analyzed through optical microscopy containing the recombinant plasmid pDMK06, when it was observed, all through the growth time, modifications on cell morphology, characterized by the formation of filaments in those induced with IPTG, in comparison with the control. For expression analysis of the recombinant protein ETKTrx, polyacrylamide gel electrophoresis SDS-PAGE was performed with the samples that grew with IPTG induction for eight hours. The results showed that the protein ETK-Trx is about 47 kDa with a high level of expression at the insoluble fraction, probably as an inclusion corpuscle. The high levels of expression of ETK-Trx protein occurred in a perfectly regulated way, showing the functionality of the pDM02 plasmid expression/regulation system.
A enteroquinase (EC 3.4.21.9) é uma serino protease heterodimérica, ativadora natural do tripsinogênio, capaz de clivar especificamente a sequência Asp-Asp-Asp- Asp-Lys. Devido à alta especificidade do sítio de reconhecimento tornou-se uma ferramenta de grande interesse biotecnológico. É comumente utilizada para a remoção in vitro de marcas de afinidade, como etiquetas de fusão (tags) de proteínas recombinantes. No presente trabalho, a estratégia de clonagem molecular resultou na construção do plasmídeo pDMK06, que é capaz de programar a expressão heteróloga regulada do gene ETK-Trx em E.coli. Por meio do processo de clivagem com as enzimas de restrição NdeI e BamHI foi possível obter a sequência codificadora da proteína de fusão entre enteroquinase e tiorredoxina (ETK-Trx) de aproximadamente 1259 pb partir do plasmídeo pENTK, a seguir essa sequência foi subclonada nos sítios de NdeI e BamHI do vetor de expressão pDM02, originando o plasmídeo recombinante pDMK06. Esse vetor contém o promotor TH2 que é regulado eficientemente pelo sistema operador/repressor Lac. Células de E.coliJM110 transformadas com o plasmídeo recombinante mostram menor crescimento em meio sólido quando a expressão da proteína heteróloga era induzida por IPTG em relação ao controle, porém esse efeito não foi detectado em meio líquido. Além disto foi analisado por microscopia ótica a morfologia das células de E.colicom o plasmídeo recombinante pDMK06, onde observou-se no decorrer do tempo de crescimento e indução, alterações na morfologia celular caracterizada de filamentação das células induzidas com IPTG quando comparadas com o controle. Para análise da expressão da proteína recombinante ETK-Trx utilizou-se a eletroforese em gel de poliacrilamida SDS-PAGE das amostras referentes a 8 horas de crescimento e indução com IPTG. Os resultados obtidos apresentaram a proteína ETK-Trx com tamanho aproximado de 47kDa com alto nível de expressão na fração insolúvel, provavelmente em forma de corpúsculo de inclusão. A expressão em altos níveis das proteínas ETK-Trx ocorreu de forma perfeitamente regulada mostrando a funcionalidade do sistema de expressão/regulação do plasmídeo pDM02.
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Silveira, Denise Sayuri Calheiros da. "Papel funcional dos leucotrienos na resposta imunológica ao melanoma B16-F0 experimental em camundongos". Universidade de São Paulo, 2012. http://www.teses.usp.br/teses/disponiveis/60/60135/tde-28062012-144450/.
Testo completoAbstract (sommario):
No presente trabalho investigamos a relevância dos mediadores lipídicos (Leucotrienos) gerados pela enzima 5-Lipoxigenase (5-LO) na susceptibilidade ou resistência de camundongos ao Melanoma experimental com células tumorais B16-F0, utilizando como modelo camundongos produtores de leucotrienos (129_WT) e camundongos geneticamente deficientes \"knockout\" de 5-LO (129_5-LO KO). Primeiramente, verificamos que leucócitos peritoneais provenientes de animais WT implantados com melanoma B16-F0, apresentam aumento da expressão do gene para 5-LO (Alox5). Nossos resultados mostram que animais 5-LO KO, deficientes de 5-LO são mais eficientes no controle da progressão do tumor e apresentam significativo aumento na sobrevivência, quando comparados a animais WT, produtores de 5-LO. A nossa análise do perfil imunológico em células esplênicas indicam que a maior eficiência dos camundongos 5-LO KO no controle do crescimento de células tumorais B16-F0 estariam associados à presença numérica aumentada de neutrófilos (Gr-1+), células apresentadoras de antígeno (I-Ab+) majoritariamente CD19+CD80+ e esplenócitos capacitados para produção de altos níveis de citocinas pró-inflamatórias/efetoras como a IL-6, TNF?, IFN-? e baixos níveis de citocinas regulatórias como IL-10, 15 dias pós-implantação do tumor; a rápida geração da resposta imune polarizada para produção elevada de citocinas Th1 (IFN-?), mas não, citocinas Th2 (IL-10) e presença de maiores números de linfócitos T CD4+ e CD8+ efetoras, expressando o fenótipo CD44high ou CD44highCD62Llow. Ainda, verificamos que a deficiência genética da 5-LO ou a inibição da 5-LO pelo MK886 em células LAK, aumenta significativamente sua atividade citotóxica em células do melanoma B16-F0. Nossos resultados em conjunto, indicam que leucotrienos gerados pela enzima 5-LO, modulam negativamente a geração de resposta imune protetora em camundongos para o Melanoma B16-F0.In the present work we examine the contribution of 5-lipoxigenase-derived lipid mediators during experimental melanoma (B16-F0) in 5-LO gene knockout (KO) mice and wild-type (WT) mice. The 5-LO KO mice presented delayed tumor growth, lesser tumor volume and delayed mortality. The greater resistance of 5-LO KO mice correlated with the following: High splenic Gr-1+ leukocytes counts, High and dominant presence of splenic IAb+CD19+CD80+ antigen-presenting cells counts and capacity of spleen cell to produce high levels of IL-6, TNF-?, IFN-? and lower levels of IL-10 early after tumor cells implantation; rapid T-cell polarization to secret high quantities of Th1 type cytokine IFN-? and low quantities of Th2 type cytokine IL-10; rapid generation and greater numbers of CD4+ and CD8+ activated T cells expressing CD45RB or CD44 markers; and also CD4+ and CD8+ CD44high or CD44highCD62Llow effector T cells. Herein, IL-2 induced splenic LAK cells from 5-LO KO mice, compared with splenic LAK cells from WT mice, were more efficient at killing B16-F0 melanoma cells. The increased B16-F0 melanoma cells killing activity were also found by treatment of splenic LAK cells from WT mice with a 5-LO activity inhibitor, MK886. Our findings suggest that 5-LO deficiency altered antigen-presenting cells profile, IFN-? and IL-10 production during skin cancer disease favoring the generation of protective immune responses and also provide evidence that 5-LO-derived LTs negatively affect the host survival during experimental B16-F0 melanoma.
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Triffaux, Emily. "Identification des canaux Cav1 impliqués dans la voie de signalisation calcique des lymphocytes Th2". Toulouse 3, 2013. http://thesesups.ups-tlse.fr/1959/.
Testo completoAbstract (sommario):
L'asthme est une maladie pulmonaire qui touche environ 10% de la population. Les lymphocytes T helper de type 2 jouent une rôle important dans la physiopathologie de l'asthme en produisant de l'interleukine 4,5,13. Mon équipe a montré dans une étude précédente que les cellules Th2 mais pas Th1 de souris exprimaient des canaux CaV1. Un oligonucléotide antisens (CaV1AS) inhibe la réponse calcique et la production de cytokines Th2 sous stimulation par le TCR sans toucher les cellules Th1 chez la souris. De plus, CaV1AS prévient l'asthme allergique expérimental. Durant ma thèse, j'ai montré que les cellules T au repos expriment CaV1. 4. Les isoformes CaV1. 2 et CaV1. 3 prédominent dans les cellules Th2 et leur expression est perdue dans les Th1. Un inhibiteur pharmacologique des canaux CaV1, un CaV1AS et CaVbAS diminue l'expression protéique de CaV1. 2 suggérant que CaVb est requis pour la stabilité des lymphocytes Th2. Finalement, l'inhibition de la PKCa/b diminue la réponse calcique et la production de cytokines par les lymphocytes Th2 mais pas Th1 suggérant que la PKC pourrait contribuer à la régulation de CaV1 dans les lymphocytes Th2. Ces résultats suggèrent que la PKC pourrait contribuer à la régulation de CaV1 dans les lymphocytes Th2. Ces résultats suggèrent que l'inhibition des canaux CaV1. 2 pourrait être bénéfique dans les maladies allergiquesAsthma is an allergic pulmonary disease which affects around 10% of the population. Allergen-specific type 2 T helper lymphocytes Th2 have a crucial role in the asthma physiopathology by producing interleukin IL4,5,13. Previously, my team reported that mouse Th2 but not Th1 cells express voltage gated calcium CaV1 channels. CaV1 channel specific antisense oligonucleotide CaV1AS inhibit calcium response and Th2 cytokine production (IL4,5,13) upon TCR stimulation without any effect on Th1 cells in mice. In addition, CaV1AS prevent experimental allergic asthma. During my PhD, I showed the CaV1. 4 expression in human resting cells. Conversely, CaV1. 2 and CaV1. 3 predominated in Th2 cells and were lost in Th1 cells. CaV1 channel inhibitors, CaV1. 2 AS and CaVbAS decreased calcium signaling and cytokine production in Th2 but not in Th1 cells. Moreover, CaVbAS decrease the CaV1. 2 protein suggesting that CaVb is required for CaV1. 2 stability in Th2 cells. Finally selective PKCa/b inhibition decreased calcium response and cytokine production by Th2 but not Th1 cells suggesting that PKC may contribute to CaV1 regulation in Th2 cells. These results suggest that the inhibition of CaV1. 2 channels could be beneficial in allergic diseases while sparing Th1 cell responses
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Zhang, Shengtao. "Klonierung, Expression und initiale Charakterisierung vom humanen TIM3". Doctoral thesis, [S.l.] : [s.n.], 2004. http://deposit.ddb.de/cgi-bin/dokserv?idn=972570357.
Testo completo
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Marinho, Claudio Romero Farias. "Correlação entre a Carga Parasitária na Fase Aguda e a Intensidade da Patologia, Parasitismo e Ativação do Sistema Imune na Fase Crônica da Doença de Chagas Experimental". Universidade de São Paulo, 1998. http://www.teses.usp.br/teses/disponiveis/42/42133/tde-11122007-114226/.
Testo completoAbstract (sommario):
0 objetivo deste trabalho foi definir se a carga parasitaria na fase aguda da doenga de Chagas experimental afeta a parasitemia, a patologia e a resposta imune na fase cr6nica. Para obtengelo de diferentes cargas parasitoirias na fase aguda, camundongos A/J foram infectados corn 103 OU 105 formas tripomastigotas de T. cruzi e analisados urn ano depois. Os animais cr6nicos infectados corn 105 formas tripomastigotas apresentaram maior nivel de parasitemia residual, maior intensidade de inflamagclo no coragtio e no moscuio esquel6tico e maior grau de ativa95o do sistema imune do que os animais infectados corn 103 formas. Em reiagclo aos parametros imuno16gicos analisados, observou-se nos animais infectados corn 105 formas: i) expansio das populag6es B220-CD5- e CD8\'; ii) freq0@ncia maior de blastos nas populag6es linfocit@rias B220\', CD8\' e CD4\'; iii) mudanga acentuada nas c61ulas CD4+ para o fen6tipo CD4+CD45RBI-ow, indicando urn aumento das c61ulas efetoras elou de mem6ria; iv) freqGC=ncias elevadas de blastos CD4+CD45RB Hig\' e CD4+CD45RB Low; vi) nomero superior de c61ulas secretoras de lg principaimente IgG2a; v) niveis superiores de anticorpos IgG2a e IgGl especificos e vii) maior produgclo de IFN-Y e de IL-4. Estes resultados indicam que a carga parasitaria na fase aguda da infecggto influencia a ativagclo do sistema imune e o desenvolvimento da patologia na fase cr6nica da doenga de Chagas.The objective of this project is to evaluate if the parasite load in the acute phase experimental Chagas\' disease affects the parasitemias, the pathology and the immune response in the chronic phase. To obtain low- and high-parasite loads in the acute phase of the disease, AlJ mice were infected with 103 or 105 T. cruzi trypomastigotes of the Y strain, and treated on day 6 with Benzonidazol. One year later, chronic mice were screened for subpatent parasitemias, tissue pathology and immune response. Mice infected with the high parasite inoculum showed higher levels of chronic parasitemias, heart and striated muscle inflammation and activation of the immune system when compared to mice infected with the low¬dose inoculum. Concerning the activation of the immune system, the main findings in high-dose infected mice were: i) increased numbers of splenocytes, with preferential expansion of CD8+ and B220-CDS- cells, many of them bearing a macrophage phenotype; ii) higher frequencies of B (B220+), CD4+ and CD8+ large lymphocytes; iii) a shift of CD4+ cells towards a CD4SRBLow phenotype; iv) increased frequencies of both CD4SRBLow and CD4SRBHigh large CD4+ cells; v) augmented numbers of total Ig-secreting cells, with predominance of IgG2a¬producing cells, and; vi) increased production of IFN-y and IL-4. In addition, these mice presented lower IgM and higher IgG2a and IgG1 parasite-specific serum antibody levels. Our results indicate that the parasite load at the acute phase of T. cruzi infection influences the activation of the immune system and development of Chagas pathology at the late chronic phase of the disease.
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Dwyer, Daniel Francis. "Effector roles of Granulocytes and B cells during Th2 Inflammation". Thesis, Harvard University, 2014. http://dissertations.umi.com/gsas.harvard:11580.
Testo completoAbstract (sommario):
Allergens are complex mixes of proteins and other compounds that have innate signaling capacity leading to Th2 inflammation. Understanding the role of each of these signals is essential to determining what separates allergens from innocuous proteins. Here, we examine two models for Th2 inflammation: infection with the helminth Trichinella spiralis and footpad immunization with papain, a cysteine protease structurally similar to proteases found in many common allergens including grass pollen and dust mites and helminth-secreted proteases secreted. Together, these studies highlight previously unappreciated effector roles of accessory cells during Th2 inflammation.
21
Xiao, Yanping. "APRIL (TNFSF13) in Th1, Th2 and Th17 Responses". Scholarly Repository, 2009. http://scholarlyrepository.miami.edu/oa_dissertations/335.
Testo completoAbstract (sommario):
The T cell function of a proliferation inducing ligand (APRIL or TNFSF13) remains unclear. By comparing APRIL-/- mice with wild type (WT) mice, we have investigated the roles of APRIL in Th1, Th2 and Th17 responses. With regard to APRIL in Th1 responses, cultured APRIL-/- CD4+ T cells showed increased IFN-gamma production under non-polarizing, but not under Th1 polarizing, conditions. No difference in antigen-specific IgG2a levels existed between APRIL-/- and WT mice immunized with ovalbumin (OVA) and complete Freund's adjuvant (CFA) which induces Th1 polarization. Our data indicate that APRIL represses Th1 responses only under non-polarizing conditions. As for APRIL in Th2 responses, cultured APRIL-/- CD4+ T cells exhibited enhanced Th2 cytokine production under non-polarizing conditions, and augmented IL-13 production under Th2 polarizing conditions. Upon immunization with OVA and aluminum potassium sulfate (alum) which induces Th2 polarization, APRIL-/- mice responded with an increased antigen-specific IgG1 response. In the OVA-induced allergic lung inflammation model which is mediated by Th2 responses, APRIL-/- mice had significantly aggravated allergic lung inflammation. Accordingly, a decoy receptor-Ig fusion protein, TACI-Ig, treatment to block APRIL in WT mice enhanced allergic lung inflammation. In agreement with the role of APRIL in CD4+ T cells, the transfer of APRIL sufficient, OVA-specific, TCR transgenic CD4+ T (OT-II) cells to APRIL-/- mice restored the suppressive effect of APRIL on allergic lung inflammation. Mechanistically, the expression of c-maf, the IL-4 gene transcription factor, was markedly enhanced in APRIL-/- CD4+ T cells under non-polarizing and Th2 polarizing conditions. Our data suggest that APRIL inhibits Th2 responses and allergic lung inflammation by suppressing IL-4 production in CD4+ T cells via diminished c-maf expression, and by suppressing IL-13 production in CD4+ T cells via an IL-4 independent, IL-13 specific pathway. Regarding APRIL in Th17 responses, the incidence of Th17-mediated collagen-induced arthritis (CIA) in APRIL-/- mice was reduced, in parallel with diminished levels of antigen-specific IgG2a autoantibody and IL-17 production. Our data indicate that APRIL promotes IL-17 production, and that APRIL-triggered signals contribute to arthritis. Our data clearly show that APRIL is important in T cell immunity, inhibitory in Th2 responses and costimulatory in Th17 responses.
22
Pearson, Joanne. "The pathological role of Th2 cytokines in artherosclerosis". Thesis, University of Oxford, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.419321.
Testo completo
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Schulz, Kerstin Ingrid. "Modulation of Th1 and Th2 type immune responses". Thesis, University of Glasgow, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.390690.
Testo completo
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Jonsson, Yvonne. "Cytokines and immune balance in preeclampsia : a survey of some immunological variables and methods in the study of preeclampsia". Doctoral thesis, Linköping : Linköpings universitet, 2005. http://www.bibl.liu.se/liupubl/disp/disp2005/med924s.pdf.
Testo completo
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Hamasato, Eduardo Kenji. "A influência da convivência com um parceiro doente sobre a resposta inflamatória alérgica pulmonar em camundongos". Universidade de São Paulo, 2016. http://www.teses.usp.br/teses/disponiveis/10/10133/tde-29092016-103925/.
Testo completoAbstract (sommario):
As relações bidirecionais entre o Sistema Nervoso e o Sistema Imune são relevantes para a manutenção da homeostase do organismo. Estudos realizados em nosso laboratório mostraram que 14 dias de coabitação com um conspecífico doente (injetado com células do tumor de Ehrlich-TAE) produziu mudanças comportamentais, endócrinas e imunológicas. Este estudo analisa os efeitos da convivência com um animal portador de tumor de Ehrlich em camundongos OVA sensibilizados e desafiados sobre a resposta alérgica pulmonar. Pares de camundongos machos foram separados em três grupos: naïve, controle e experimental. Os animais do grupo naïve não foram manipulados sendo utilizados para a avaliação de parâmetros basais. Um animal de cada par dos grupos experimental e controle foi imunizado com OVA. No dia D(0), os animais imunizados receberam uma dose reforço de OVA. No dia D(0) os camundongos do grupo experimental que não foram manipulados foram inoculados com 5x106 células de tumor de Ehrlich; seus companheiros de gaiola moradia foram designados CAD (companheiro do animal doente). Os camundongos não perturbados de cada par do grupo controle foram tratados (i.p.) em D(0) com 0,9% de NaCl, sendo designados CAS (companheiro do animal saudável). O desafio intranasal com OVA foi realizado nos camundongos CAS e CAD nos dias D(12) e D(13); colheram-se o sangue e os tecidos no dia D(14). Em comparação com o grupo CAS, os camundongos do grupo CAD apresentaram 14 dias após a coabitação: (1) aumento do número de eosinófilos e neutrófilos no LBA, (2) diminuição na contagem de células da medula óssea, (3) aumento do níveis de IL-4 e IL-5 e diminuição de IL-10 e INF-ϒ no sobrenadante do LBA, (4) aumento dos níveis de IgG1-OVA, diminuição dos níveis de IgG2a-OVA e nenhuma alteração na IgE-OVA no sangue periférico, (5) aumento na expressão de ICAM-1, VCAM-1 e L-selectina em granulócitos do LBA, (6) diminuição da reatividade da traquéia à metacolina in vitro, (7) aumento da desgranulação de mastócitos, (8) nenhuma alteração nos níveis plasmáticos de corticosterona, (9) aumento dos níveis de adrenalina e noradrenalina plasmáticas, (10) diminuição no tempo de permanência e entradas nos braços abertos do labirinto em cruz elevado, (11) diminuição da expressão de IL-6 no PVN e (12) diminuição da expressão de C-fos no PFC. Estes resultados mostram que a convivência forçada com um animal portador de um tumor ascitico de Ehrlich exacerba a inflamação alérgica pulmonar de camundongos. Eles foram discutidos como decorrentes da estimulação do Sistema Nervoso Autônomo Simpático (SNS) pelo estresse psicológico gerado pela coabitação com o parceiro doente, via liberação de adrenalina e noradrenalina e consequente mudança no perfil de citocinas Th1/Th2 para uma resposta do tipo Th2. Esta alteração seria, provavelmente, um dos mecanismos responsáveis pelo aumento do recrutamento celular para as vias aéreas dos camundongos do grupo CAD.The bidirectional relationship between the nervous system and the imune system is relevant for homeostatic organism maintenance. Studies from our laboratory showed that 14 days of cohabitation with a sick conspecific (injected with Ehrlich tumor cells-TAE) produced behavioral, endocrinological and immunological changes. This study analyzes the effects of cohabitation with an Ehrlich tumor-bearing animal on ovalbumin (OVA)-induced lung inflammatory response in mice. Pairs of male mice were separate into three groups: naïve, control and experimental. Animals of the naïve group were kept undisturbed being used for assessment of basal parameters. One animal of each experimental and control pair of mice was immunized with OVA. On D(0), these OVA-immunized animals received an OVA booster. At this day (D(0)) the experimental mice that were kept undisturbed were inoculated with 5x106 Ehrlich tumor cells; their immunized cage-mates were then referred as to CSP(companion of sick partner). The undisturbed mice of each control pair were i.p. treated on D(0) with 0.9% NaCl; their sensitized cage-mate were subsequently referred as CHP (companion of health partner). The intranasal OVA challenge was performed on CSP and CHP mice on D(12) and D(13); blood and tissue collection were performed on D (14). Fourteen days after cohabitation, in comparison to the CHP mice, the CSP mice displayed the following: (1) an increased number of eosinophils and neutrophils in the BAL, (2) a decreased bone marrow cell count, (3) increased levels of IL-4 and IL-5 and decreased levels of IL-10 and INF-ϒ in the BAL supernatant, (4) increased levels of IgG1-OVA, decreased levels of IgG2a-OVA and no changes in OVA-specific IgE in the peripheral blood, (5) increased expression of ICAM-1, VCAM-1 and L-selectin in the BAL granulocytes, (6) decreased tracheal reactivity to metacholine measured in vitro , (7) increased mast cell degranulation, (8) no changes in plasma corticosterone levels (9) increased levels of plasmatic adrenaline and noradrenaline, (10) decreased time and % of entries on open arms of elevated plus maze, (11) decreased expression of IL-6 on PVN and (12) decreased expression of C-fos on PFC. These results suggest that cohabitation with an Ehrlich tumor bearing mice exacerbates allergic lung inflammatory response in mice. Most probably, the changes observed in CSP mice are a consequence of the psychological stress induced by forced cohabitation with the sick partner. Strong involvement of the sympathetic nervous system through adrenaline and noradrenaline release and a shift of the Th1/Th2 cytokine profile toward a Th2 response were considered to be the mechanisms underlying the cell recruitment to the animal´s airways.
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Walwyn-Brown, Katherine. "Control of Th2 polarisation by dendritic cells and natural killer cells". Thesis, University of Manchester, 2018. https://www.research.manchester.ac.uk/portal/en/theses/control-of-th2-polarisation-by-dendritic-cells-and-natural-killer-cells(fd15f834-f926-40f1-88ff-217bf1fbf263).html.
Testo completoAbstract (sommario):
Type 2 (Th2) immune responses are required for immune defence against helminths, but can also have pathogenic effects in allergic conditions. This thesis examined two factors which may influence Th2 immunity at a cellular and molecular level: cross-talk between Natural Killer (NK) cells and dendritic cells (DCs) and the cell surface organisation of DCs. Cross-talk between NK cells and DCs is well-established to impact Th1 responses against tumours and infection; however the influence of this interaction during Th2 inflammation is unknown. To investigate this, human monocyte-derived DCs were stimulated in vitro with different pathogen-associated molecules; LPS or Poly(I:C) which polarise a Th1 response, or soluble egg antigen (SEA) from the helminth worm Schistosoma mansoni, a potent Th2-inducing antigen. These cells were then combined with autologous NK cells. Confocal microscopy showed polarisation of the NK cell microtubule organising centre (MTOC) and accumulation of LFA-1 at contacts between NK cells and immature or Th2-polarising DCs, but not Th1-polarising DCs, indicative of the assembly of an activating immune synapse. NK cells did not lyse DCs treated with LPS or Poly(I:C), but degranulated to and lysed both immature DCs and Th2 polarising DCs. Antibody blockade of NK cell activating receptors NKp30 and DNAM-1 prevented this lysis. Furthermore, depletion of NK cells in mice which were then transferred with Th2 polarising DCs led to an enhanced Th2 recall response. Thus, these data indicate a previously unrecognised role of NK cell cytotoxicity in restricting the pool of DCs involved in Th2 immune responses. Secondly, this thesis investigated the nanoscale organisation of MHC-II on the surface of Th1 and Th2 polarising DCs using ground state depletion super-resolution microscopy. MHC-II was relatively homogenously distributed across the membrane with no significant changes in clustering between immature, Th1 and Th2 polarising DCs. In contrast, imaging CD74, which can mediate internalisation of MHC-II, revealed increased expression and a more homogenous distribution of this receptor on the surface of Th2-polarising DCs compared to Th1-polarising DCs. These data suggest that changes in the clustering of CD74 could modulate MHC-II surface expression during Th2 responses. Overall, the results in this thesis indicate that both molecular and cellular level modulation of DC function contribute to the development of Th2 responses.
27
MERLOT, Élodie. "Modulation de la production de cytokines par l'environnement". Phd thesis, Institut national agronomique paris-grignon - INA P-G, 2003. http://tel.archives-ouvertes.fr/tel-00007518.
Testo completoAbstract (sommario):
Les conséquences immunitaires d'un stress d'origine environnementale sont complexes et encore difficilement prévisibles. Le stress affecte le système immunitaire soit en agissant sur l'immunité innée, en altérant la réactivité inflammatoire, soit en agissant sur l'immunité acquise, en modulant la production de cytokines dites Th1 et Th2. L'environnement socialcontribue largement au développement et à l'expression de maladies. Dans les espèces sociales, la position sociale occupée dans le groupe module la susceptibilité aux infections mais les supports endocriniens et immunitaires de ces différences de susceptibilité sont ignorés. La remise en cause de l'organisation sociale engendre un stress important dont les conséquences immunitaires sont encore sujettes à controverse.
Ce travail de thèse a pour objectifs (1) de décrire l'influence du statut social sur le fonctionnement des systèmes endocrinien et immunitaire, (2) de préciser les effets du stress
social sur la production de cytokines et la susceptibilité aux infections et (3) de rechercher des facteurs à l'origine de la variabilité des conséquences immunitaires du stress social.
Chez le porcelet, un regroupement après le sevrage élève transitoirement le cortisol salivaire et altère le comportement mais n'affecte pas la réactivité des lymphocytes sanguins.
La suite des travaux a utilisé une procédure de défaite sociale chronique chez la souris. Les résultats obtenus mettent en évidence une influence du statut social. En absence de stress, les
dominants présentent des niveaux de base de corticostérone et une réponse spécifique à la tuberculine supérieurs aux dominés. Suite à une défaite sociale, les dominants sont plus affectés que les dominés. La défaite sociale augmente la réactivité inflammatoire mais ne modifie pas de façon nette l'équilibre de la production de cytokines de type Th1 et Th2 et n'affecte pas l'immunité spécifique développée contre une infection mycobactérienne. Les conséquences immunitaires de la défaite sociale ne sont observées que lorsque le stress est associé à des combats et à des blessures. Ces travaux montrent que la réponse au stress dépend de l'histoire sociale de l'individu, en particulier de son statut social. De plus, les
répercussions immunitaires du stress dépendent aussi de l'histoire immunitaire récente. En effet, une réaction inflammatoire systémique inhibe la libération plasmatique de cytokines
inflammatoires en réponse à un stress psychologique ultérieur.
28
Bock, Cristin Nadine [Verfasser]. "Identification and characterization of murine and human Th2/1 hybrid cells in Th2-driven diseases / Cristin Nadine Bock". Berlin : Freie Universität Berlin, 2019. http://d-nb.info/1199343862/34.
Testo completo
29
Espinosa, Karina. "CysLT1R modulation by Th1 Th2 and Th3 type cytokines in BSMC". Mémoire, Université de Sherbrooke, 2002. http://savoirs.usherbrooke.ca/handle/11143/3304.
Testo completoAbstract (sommario):
L'inflammation asthmatique chronique est caractérisée par le remodelage des voies aériennes, la dénudation de l'épithélium, l'épaississement des parois bronchiques, la fibrose sous-épithéliale, la métaplasie des glandes à mucus, ainsi que par l'hyperplasie et l'hypertrophie des muscles lisses bronchiques. Certaines études suggèrent un rôle possible pour les cystéinyl-leucotriènes (CysLTs) dans le remodelage des voies aériennes. Ce travail vise à caractériser la modulation du récepteur CysLT1 (CysLT1R) par des cytokines de type Th1, Th2 et Th3 dans un processus fonctionnel tel que le remodelage des voies aériennes. Méthodes . L'expression du CysLT1R dans des cellules de muscle lisse bronchique humaines (CMLB) provenant de cultures primaires a été évaluée par cytométrie de flux, avec un anticorps polyclonal anti-CysLT1R, après stimulation avec les cytokines pendant 24h. Une analyse par microscopie de fluorescence a été effectuée pour compléter les résultats obtenus par la cytométrie de flux. L'expression de l'ARNm de CysLT1R a été mesurée par RT-PCR à l'aide d'amorces spécifiques pour ce récepteur et pour GAPDH. La prolifération a été évaluée par une analyse colorimétrique dans des cellules traitées pendant 24h avec les cytokines puis pendant 72h avec LTD 4. Résultats. L'expression de CysLT1R chez les CMLB a été modulée à la hausse par TGF-[bêta], IL-13 et IFN-[gamma]. IL-13 et IFN-[gamma], mais pas TGF-[bêta], ont augmenté l'expression de l'ARNm de CysLT1R. La modulation à la hausse de CysLT1R induite par TGF-[bêta] et IL-13 a augmenté la prolifération des CMLB en réponse à LTD 4 . L'antagoniste de CysLT1R, Montelukast, a inhibé cet effet, ce qui suggère que l'effet de prolifération est sélectif pour CysLT1R. Ensemble, nos résultats soutiennent le rôle des CysLTs dans le remodelage des voies aériennes observé chez les patients asthmatiques.
30
Hall, Gillian. "Approaches for the modulation of allergen-specific TH2 immunity". Thesis, University of Edinburgh, 2003. http://hdl.handle.net/1842/24666.
Testo completoAbstract (sommario):
The prevalence of allergic diseases, such as asthma, rhinitis, eczema and food allergies has increased dramatically over the last few decades and is now a major health and economic burden throughout the developed and developing worlds. Type I (immediate) hypersensitivity reactions are mediated by immunoglobulin E (IgE) responses directed against innocuous environmental antigens, such as pollen, housedust mites or animal dander. It is the resulting release of pharmacological mediators by IgE-sensitised mast cells that cause the symptoms of asthma and allergic rhinitis. The induction of IgE is dependent on CD4+ T cells of the Th2 phenotype which are characterised by the production of specific cytokines (IL-4, IL-5 and IL-13). In contrast, the presence of allergen reactive Thl cells, which secrete IFN-y, in nonallergic healthy individuals suggests that Thl immunity is not damaging to the host and is possibly associated with protective immunity. It is clear with the high incidence of atopic disorders combined with existing treatments, which are in general symptomatic, that there is a requirement for new therapeutic agents. Since CD4+ T cells play an important role in the response to allergens they are an obvious target for drug development and they can be targeted directly, with the aim of inducing specific tolerance. A second strategy for inhibiting the synthesis of Th2 cytokines may be achieved by promoting the induction of Thl immunity. Therefore, the main aim of this study was to investigate these different approaches for the modulation of Th2 immunity to the major house dust mite allergen Der p 1. Tolerance induction or the promotion of Thl responses were attempted by intranasal delivery of antigen alone, by the systemic or mucosal delivery of Der p 1 in PLG polymer microparticles (MEA) and finally, by intranasal administration with chitosan, an enhancer of epithelial permeability. In order to investigate the efficacy of the regimens of vaccination, an adjuvant free model of Th2 cytokine-mediated allergic inflammation was developed in vivo in H-2b mice. Vaccination with microencapsulated antigen failed to elicit a Thl response or induce tolerance despite altering the kinetics, dose and method of delivery. In fact, the Th2 phenotype was usually exacerbated following administration of MEA/Der p 1 particles. Intranasal co-administration of antigen with chitosan inhibited Th2 cytokine production but not as a result of the tolerance induction. Similarly, high doses of soluble peptide delivered intranasally, failed to tolerise allergen-specific Th2 immunity. In conclusion, the redirection of the Th2 immune response and the induction of tolerance were difficult to achieve. However, chitosan which was not as extensively researched as the other approaches may prove to be of therapeutic value.
31
Kinyanjui, Margaret. "Targeting Th2 transcription factors in experimental asthma". Thesis, McGill University, 2008. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=18717.
Testo completoAbstract (sommario):
Antigen specific CD4+ T cells adoptively transfer airway inflammation comprised mainly of lymphocytes and eosinophils. The ability of these transferred T cells to induce inflammation is dependent on the cytokines they express particularly Th2 cytokines. In order to better understand the mechanism by which adoptively transferred T cells induce airway inflammation, we chose to modulate the expression (GATA-3) and activity (STAT-6) of two key regulators of Th2 cytokine production. To modify expression of GATA-3, we used a bicistronic retroviral vector encoding GATA-3 and enhanced green fluorescent protein (EGFP). As a control, we used a retrovector encoding EGFP alone. By coupling in vitro antigen stimulation with retroviral transduction we generated antigen specific CD4+ T cells expressing EGFP alone or GATA-3 and EGFP. When transferred into naïve recipients that were subsequently challenged, these transduced CD4+ T cells induced lung inflammatory responses with an increase in both CD4+ lymphocytes and eosinophils. This antigen specific inflammatory response was enhanced in animals receiving T cells overexpressing GATA-3. Analysis of the infiltrating cells also revealed that the EGFP+ T cells were present in the lung following antigen challenge, comprising only a small fraction of the CD4+ T cells recruited to the lung during the antigen response. Thus, GATA-3 amplifies antigen-specific inflammatory responses in the airways by augmenting the ability of antigen specific T cells to recruit inflammatory cells to the lung following antigen challenge. To modify the activity of STAT-6 we used chimeric cell penetrating peptides containing a poly-arginine protein transduction domain (PTD) coupled to a sequence predicted to bind and inhibit STAT-6 activity (SIP-1). Using fluorescein-tagged SIP-1, we demonstrate that the poly-arginine PTD efficiently translocates to the cytoplasm within an hour. In vitro, antigen-induced IL-4 production was inhibited in SIP-1-treated splenoLes cellules CD4+ T à antigènes spécifiques transfèrent par adoption l'inflammation pulmonaire constituées principalement de lymphocytes et d'éosinophiles. L'habileté de celles-ci à transférer des cellules T pour induire l'inflammation est dépendante de leur expression de cytokines Th2. De manière à mieux comprendre le mécanisme par lequel les cellules T transmises par adoption induisent l'inflammation pulmonaire, nous avons choisi de moduler l'expression de GATA-3) ou l'activité de (STAT-6) des deux régulateurs-clés de production de cytokine Th2. Afin de modifier l'expression de GATA-3 dans les cellules T destinées au transfert par adoption, nous avons utilisé un rétrovirus recombinant concentré avec une filtration par centrifugeuse. Ce procédé a dramatiquement augmenté leurs titres et ainsi leur habileté à transduire les cellules CD4+ T en culture primaire. Nous avons utilisé un rétrovirus recombinant qui encode la GATA-3 et / ou la protéine fluorescente verte (EGFP). En couplant in vitro la stimulation d'antigènes avec la transduction par vecteur viral, nous avons généré des cellules CD4+ T à antigènes spécifiques exprimant de l'EGFP seul ou bien de la GATA-3 et de l'EGFP. Lorsque transféré dans un rat qui avait subséquemment été provoqué avec des antigènes, ces cellules CD4+ T induisent une réaction aux inflammations pulmonaires avec une augmentation des lymphocytes et éosinophiles. Cette réaction inflammatoire fut accrue chez les animaux recevant les cellules T surexprimant la GATA-3. L'analyse des cellules infiltrantes a aussi révélé que bien que les cellules EGFP+ étaient présentes dans les poumons suivant la provocation par antigènes, elles étaient constituées seulement d'une petite fraction de cellules CD4+ T recrutées dans les poumons. Ainsi, la GATA-3 amplifie la réaction inflammatoire des poumons induite par antigènes en augmentant l'habileté des cellules T à antigènes spécifiques à recruter
32
Vallabh, Sushmitha. "Targeted Epigenetic Suppression of Th2 Cytokines Expression". University of Cincinnati / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1505131225205869.
Testo completo
33
Stock, Philippe [Verfasser]. "Immunregulation bei Th2 gerichteten Erkrankungen / Philippe Stock". Berlin : Medizinische Fakultät Charité - Universitätsmedizin Berlin, 2009. http://d-nb.info/102349468X/34.
Testo completo
34
Lécart, Sandrine. "Caractérisation phénotypique et fonctionnelle des lymphocytes T auxiliaires humains, producteurs d'IL-10 : Th2 et T régulateurs (Tr)". Montpellier 1, 2002. http://www.theses.fr/2002MON1T004.
Testo completoAbstract (sommario):
UN MODELE IN VIVO D'INDUCTION DE REACTIONS D'HYPERSENSIBILITE CUTANEE, PROVOQUEES PAR L'HAPTENE DNCB, A ETE DEVELOPPE SUR DES SUJETS SAINS. IL A PERMIS L'ETUDE, IN VIVO, DE LA REGULATION INFLAMMATOIRE PAR L'APPARITION DE SOUS-POPULATIONS LYMPHOCYTAIRES T AUXILIAIRES DE TYPE 1, 2 ET T REGULATRICES (Tr), PRESENTANT DES PROFILS DE PRODUCTION CYTOKINIQUE STABLES ET SPECIFIQUES. PARMI LES DIFFERENTES MOLECULES DE SURFACE UTILISEES POUR CARACTERISER CES SOUS-POPULATIONS LYMPHOCYTAIRES T, NOUS AVONS MONTRE QUE LES RECEPTEURS A L'IL-12 ET A L'IFN-γ, EXPRIMES SPECIFIQUEMENT ET RESPECTIVEMENT SUR LES CELLULES TH1 ET TH2, SE DETECTENT AUSSI A LA SURFACE DES CLONES Tr ACTIVES. [. . . ] LES ANALYSES FONCTIONNELLES DES CLONES Tr ONT MONTRE QUE LEUR ACTIVITE IMMUNOSUPPRESSIVE ETAIT ASSOCIEE, AU MOINS EN PARTIE, A LEUR FORTE PRODUCTION D'IL-10. ENFIN NOS RESULTATS INDIQUENT QUE LA CYTOKINE IL-22, MALGRE SON HOMOLOGIE STRUCTURALE AVEC L'IL-10 ET LA PARTICIPATION DE LA CHAINE IL-10R2 A SON COMPLEXE RECEPTEUR, N'EST PAS IMPLIQUEE DANS LA REGULATION DE LA PRODUCTION D'IMMUNOGLOBINES PAR LES CELLULES B HUMAINES ACTIVEES. BIEN QUE LES CELLULES B ACTIVEES EXPRIMENT L'ARNm DU RECEPTEUR SOLUBLE IL-22RA2, LE MESSAGER DU RECEPTEUR TRANSMEMBRANAIRE FONCTIONNEL IL-22RA1 N'A PAS ETE DETECTE DANS CES CELLULES B.
35
Mukherjee, Sumanta. "LPS induced TH2 (Interleukin-4) cytokine production in macrophages and its regulation". University of Toledo Health Science Campus / OhioLINK, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=mco1207743729.
Testo completo
36
Persson, Marie, Christina Ekerfelt, Jan Ernerudh, Leif Matthiesen, Maria Jenmalm, Yvonne Jonsson, Martina Sandberg e Göran Berg. "Increased circulating paternal antigen-specific IFN-γ- and IL-4-secreting cells during pregnancy in allergic and non-allergic women". Linköpings universitet, Klinisk immunologi, 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-16134.
Testo completoAbstract (sommario):
INTRODUCTION: Allergic women have been reported to give birth to more children than non-allergic women, speculatively explained by the former's predisposition for Th2 polarization, possibly favoring pregnancy. AIM: The aim of this study was to test the hypothesis that allergy is associated with more Th2-deviated responses to paternal antigens throughout pregnancy. METHODS: Blood samples were collected on six occasions during pregnancy and two occasions postpartum (pp). Of the 86 women initially included, 54 women had a normal pregnancy and completed the sampling procedures. Eleven women fulfilled the strict criteria for allergy (allergic symptoms and circulating IgE antibodies to inhalant allergens) and 23 were strictly non-allergic (non-sensitized without symptoms). The numbers of blood mononuclear cells secreting IFN-gamma and IL-4, spontaneously and in response to paternal alloantigens, were compared between the groups. RESULTS: The numbers of spontaneously as well as paternal antigen-induced IFN-gamma- and IL-4-secreting cells were similar in allergic and non-allergic pregnant women on all occasions. A similar increase in the numbers of both IFN-gamma- and IL-4-secreting cells were found in allergic and non-allergic women during pregnancy, both regarding spontaneous and paternal antigen-induced secretion. CONCLUSIONS: This study does not support the hypothesis of a more pronounced Th2-deviation to paternal antigens in allergic pregnant women compared with non-allergic pregnant women, as measured by number of cytokine-secreting cells. The observed increase of both IFN-gamma- and IL-4-secreting cells during normal pregnancy may be interpreted as a Th2-situation, since the effects of IL-4 predominate over the effects of IFN-gamma.
37
Hu, Tuan Jun. "Tim family of molecules in the chicken : important differences from mammals". Thesis, University of Edinburgh, 2014. http://hdl.handle.net/1842/9621.
Testo completoAbstract (sommario):
T cell immunoglobulin and mucin (Tim) family molecules are cell membrane proteins with four functional Tim family members in mouse, and three in human. They are preferentially expressed on immune cells with Tim1 on Th2 cells, Tim3 on Th1 cells and Tim4 on antigen-presenting cells (APCs). They have several roles, including regulating immune responses and mediating phagocytosis of dead cells. However, little is known about them beyond these two species, and nothing outside mammals. To investigate the Tim family in the chicken, the genes were identified and cDNAs cloned. Differently to mammals, the chicken genome only contains genes for Tim1 and Tim4. Chicken Tim1 (chTim1) has similar mRNA expression patterns to those of mammalian Tim1 in lymphoid tissues and immune cells. Interestingly, chTim4 has at least four splice variants – an extra short isoform (chTimeS) lacking exons 5, 6, 7 and 8, a short isoform (chTim4S) without exons 3, 4 and 5, a long isoform (chTim4L) with all exons and an extra long isoform (chTim4eL), which is similar to chTim4L but with a longer exon 3. The chTim4S is a homologue of mammalian Tim4 with constitutive expression in lymphoid tissues and immune cells; other chTim4 variants showed inducible or cell-specific expression patterns. Like mammalian Tim4, chTim4S is expressed by APCs; but differently to mammals, chTim4S is also expressed by γδ T cells, suggesting a unique role for chTim4 in this population of T cells. The biological activities of the chicken Tim family molecules were also investigated using chTim-Ig fusion proteins. Like mammals, chTim1 and chTim4S fusion proteins can specifically recognise phosphatidylserine (PS), an indicator of apoptotic cells, suggesting they are PS receptors. Pre-incubation with PS blocked binding of the chTim4S fusion protein to PS-exposing apoptotic cells. Physiologically, recognition of PS by the chTim proteins mediates apoptotic cell clearance, which was demonstrated using chTim-transfected fibroblast cells (3T3), which significantly increased their uptake of apoptotic cells compared with untransfected cells. The chTim4-Ig fusion protein also had costimulatory activity on chicken T cells. Monoclonal antibodies against the chTim proteins were generated. They specifically recognise their own antigen tested intensively by different immunological assays. ChTim4L is expressed intracellularly in freshly-isolated splenocytes rather than on the surface, whereas PMA-stimulated splenocytes express chTim4S and chTim4L on the cell surface. Like mammals, chicken splenic macrophages also express chTim4S and chTim4L. Both of them are also expressed by bone marrow-derived macrophages but not bone marrow-derived DCs. The chTim1 protein was detected at high levels in bursal cells and splenocytes by western blot analysis using polyclonal anti-chTim1 serum, which is consistent with its mRNA expression pattern through qRT-PCR analysis, suggesting B and T cells may express chTim1, consistent with its expression in mammals. Mammalian Tim1 is expressed on Th2 cells, its ligand, Tim4, on APCs; the interaction between them drives Th2 cell proliferation. The knowledge from this study will help to further dissect how the chicken’s Th2 responses are regulated through cell surface molecules.
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Phythian-Adams, Alexander Thomas Luke. "Importance of dendritic cells during Schistosoma mansoni infection". Thesis, University of Edinburgh, 2011. http://hdl.handle.net/1842/5288.
Testo completoAbstract (sommario):
Infection with the helminth parasite Schistosoma mansoni leads to chronic inflammation and Th2 mediated fibrosis, which result in severe pathology characterised by hepatosplenomegaly. Dendritic cells (DCs) are adept initiators of CD4+ T cell responses, but their fundamental importance in this regard in Th2 settings remains to be demonstrated. Indeed, the role of DCs at different stages of infection with S. mansoni is also yet to be determined. In addition, the importance of the interaction of DCs with tissue factors in the tissue microenvironment on the development of Th2 response to S. mansoni antigens is an area of active research and debate. This thesis is comprises of four studies. The first study tackles the involvement and importance of DCs in the induction and development of Th2 responses against S. mansoni using CD11c–diphtheria toxin receptor mice to deplete CD11c+ cells during the priming stage of the CD4+ Th2 response against S. mansoni. Diphtheria toxin treatment significantly depleted CD11c+ DCs from all tissues tested, with 70-80% efficacy. Even this incomplete depletion resulted in dramatically impaired CD4+ T cell production of Th2 cytokines, altering the balance of the immune response and causing a shift towards IFN-γ production. In contrast, basophil depletion using Mar-1 antibody had no measurable effect on Th2 induction in this system. These data underline the vital role that CD11c+ antigen presenting cells can play in orchestrating Th2 development against helminth infection in vivo, a response that is ordinarily balanced so as to prevent the potentially damaging production of inflammatory cytokines. The second study addresses whether the exposure of DCs to the cercarial stage of the parasite is critical for either parasite survival or the subsequent development of the Th2 immune response against later stages of infection. It was found that CD11c depletion prior to infection resulted in increased parasite survival, but did not impair the development of CD4+ T cell Th2 response later in infection. The third study asked whether DCs continue to be necessary for the maintenance of the chronic immune response during infection with S. mansoni. In contrast, depletion of CD11c+ cells during the initiation (4 to 6 weeks) or maintenance (6 to 8 weeks or 12 to 14 weeks) of Th2 response to eggs, resulted in severely impaired Th2 cytokine production. Interestingly, depletion during the later stages of infection led to dramatic weight loss and mortality, coincident with impaired CD4+ T cell responses. These data suggest that CD11c+ antigen presenting cells, in addition to being important in the early priming phase, also play a vital role in the maintenance and homeostasis of chronic CD4+ T cell responses in a Th2 infection setting, the disruption of which can have lethal consequences. The final study in this thesis aimed to establish whether the tissue factor thymic stromal lymphopoietin (TSLP) is able to enhance or modulate the Th2 responses initiated by DCs stimulated with SEA. Contrary to previous studies, it was found that BMDCs do not become phenotypically activated by TSLP, in particular, they do not up-regulate the costimulatory molecule OX40L, nor does TSLP suppress the production of IL-12p40 or IL-12p70 in response to LPS or CpG. Further, exposure to TSLP had no impact on DC cytokine production or survival. Irrespective of this unaltered profile in vitro, TSLP exposed DCs transferred in vivo induced the production of significantly more Th1 and Th2 cytokines from polyclonally restimulated splenocytes than DCs exposed to medium alone. In addition to this, TSLP altered the kinetic of the immune response induced by DCs stimulated with the soluble egg antigen (SEA) of S. mansoni. This was characterised by the antigen specific production of T cell cytokines starting more rapidly than with non-TSLP treated control DCs. The alteration in the kinetics of the immune response was not restricted to Th2 antigens and was also seen to some extent in Propionibacterium acnes stimulated DCs. This suggests a possible role for TSLP in either inducing faster DC migration or greater production of T cell chemoattractants and thus, enhancing the rate of DC interaction with T cells.
39
Bender, Orissa. "Untersuchungen zur Expression des TIM-3 Moleküls auf murinen T-Helfer-Zellen". Doctoral thesis, Humboldt-Universität zu Berlin, Mathematisch-Naturwissenschaftliche Fakultät I, 2003. http://dx.doi.org/10.18452/14915.
Testo completoAbstract (sommario):
Die von T-Helfer (Th) -Zellen produzierten Zytokine spielen eine entscheidende Rolle bei der Einleitung, der Aufrechterhaltung und der Regulation von Immunantworten. Bei der Untersuchung von Immunantworten hat sich eine vereinfachte Einteilung der Th-Zellen in zwei Klassen als hilfreich erwiesen: Th1 und Th2. Stabil differenziell exprimierte Oberflächenmoleküle werden benötigt, um lebende Th1- und Th2-Zellen identifizieren, auf Einzelzellebene charakterisieren und möglicherweise die von ihnen erzeugten Immunantworten modulieren zu können. Auf der Suche nach solchen Molekülen wurde in Zusammenarbeit mit der Firma Millennium Pharmaceuticals das Oberflächenmolekül TIM-3 entdeckt. Die Ergebnisse der vorliegenden Arbeit belegen, dass TIM-3 nicht nur von CD4+ Th-Zellen, sondern auch von CD8+ T-Zellen, gamma/delta-T-Zellen, sowie einigen Makrophagen und der Mehrheit der dendritischen Zellen in der Milz von Mäusen auf der Zelloberfläche exprimiert wird. Die Expression von TIM-3 auf Th-Zellen ist klar mit einem aktivierten Phänotyp assoziiert. TIM-3 wird unter polarisierenden Bedingungen in vitro im Vergleich zu Th2-Zellen bevorzugt, jedoch nicht ausschließlich von Th1-Zellen exprimiert. Erstmals wurde auf Einzelzellebene die Zytokinproduktion TIM-3 exprimierender Th-Zellen untersucht. Die Analyse von Th0-Zellen, welche unter nichtpolarisierenden Bedingungen in vitro hergestellt wurden, ergab keine bevorzugte Produktion von Th1-Zytokinen und keine verminderte Expression von Th2-Zytokinen durch TIM-3 exprimierende Th-Zellen. Aufgrund der in dieser Arbeit erhaltenen Ergebnisse erlaubt die Expression von TIM-3 allein daher nicht die Identifizierung von Th1-Zellen. Nach einer Infektion mit Toxoplasma gondii lag jedoch eine bevorzugte Assoziation zwischen der Expression von TIM-3 und der pathogenspezifischen Produktion von Interferon (IFN)-gamma, Interleukin (IL)-2 und Tumor Nekrose Faktor (TNF)-alpha vor. Somit korreliert die TIM-3 Expression auf Th-Zellen nur unter bestimmten Bedingungen mit einem Th1-Phänotyp.The cytokines that are produced by T helper (Th) cells are decisive for the initiation, the maintenance and the regulation of immune responses. A simplified classification of Th cells has proven to be useful for the analysis of immune responses: Th1 and Th2. Stably and differentially expressed surface molecules are required for the identification of live Th1- and Th2-cells, their characterisation at the single cell level and the possible modulation of the immune responses that they induce. On the search for such molecules the surface molecule TIM-3 was discovered in collaboration with Millennium Pharmaceuticals. The present work shows that TIM-3 protein is not only expressed on the cell surface by CD4+ Th cells but also by CD8+ T cells and gamma/delta T cells as well as by some macrophages and the majority of the dendritic cells in the murine spleen. TIM-3 expression on Th cells is clearly associated with an activated phenotype. Under polarising conditions in vitro TIM-3 is expressed preferentially albeit not exclusively by Th1 cells compared to Th2 cells. For the first time, the cytokine production of TIM-3 expressing Th cells has been analysed at the single cell level. The analysis of Th0 cells, generated under non-polarising conditions in vitro showed no preferential production of Th1-cytokines and no diminished production of Th2-cytokines by TIM-3 expressing Th-cells. The results obtained in this work lead to the conclusion that expression of TIM-3 does not permit the identification of Th1-cells. However upon infection with Toxoplasma gondii a positive association between the expression of TIM-3 and the pathogen-specific production of Interferon (IFN)-gamma, Interleukin (IL)-2 and Tumor Necrosis Factor (TNF)-alpha was observed. Therefore the expression of TIM-3 on Th-cells only correlates under specific conditions with a Th1-phenotype.
40
Gold, Wendy Anne Clinical School St Vincent's Hospital Faculty of Medicine UNSW. "Characterisation of inflammatory markers and the Th1/Th2 response in localized scleroderma". Awarded by:University of New South Wales. Clinical School - St Vincent's Hospital, 2008. http://handle.unsw.edu.au/1959.4/41534.
Testo completoAbstract (sommario):
Scleroderma is a chronic autoimmune connective tissue disease of unknown etiology characterized by excessive fibrosis and is broadly divided into two clinical entities: localized scleroderma (LSc) and systemic sclerosis (SSc). SSc is a multi-system disease resulting in both skin and visceral organ fibrosis. The more benign disorder, LSc is for the most part self-limited with the disease pathology being confined to the skin and subcutaneous tissues. Proposed factors involved in the pathogenesis of these disorders include endothelial cell injury and dysfunction, immunological alterations and inflammatory activation, and abnormal ECM production by activated fibroblasts. However, the initiating mechanisms that leads to these changes remains largely unknown. This thesis examines the hypothesis that the transcriptional expression at the edge and centre of expanding LSc plaques could represent the metabolic changes involved in the different stages of disease. The major finding of this thesis was the identification of two panels of genes that showed significant changes in expression between LSc patients and healthy controls irrespective of whether the sample was taken from a diseased or clinically unaffected area of the patient. The first panel consisted of inflammatory genes including those genes characteristic of the Thl response and those induced by NF-KB. The Thl response was supported by an increased infiltration of CD4+ T cells in the LSc patients. The second panel consisted of a subset of array identified genes (scleroderma Signature) in SSc patients. Of interest, WIF1 was down regulated in both disorders and showed a gradual decrease in expression across the clinically different areas of the LSc patients. Both panels of genes showed the biggest changes of expression at the edge of the plaque suggesting their involvement in the initiating events of the disease. These results suggest that, like SSc, the underlying pathology of LSc is related to systemic changes in genes controlling amongst others, immunological and inflammatory responses. This information not only sheds light on the mechanisms involved in the initiation and progression of scleroderma, but could also contribute to the creation of a diagnostic test for the early detection of sufferers of this rare, but important disease.
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Szymczak, Wendy A. "The Role Of Chemokines and Dendritic Cells In Regulation of IL-4 and Fungal Immunity". University of Cincinnati / OhioLINK, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1266607502.
Testo completo
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Janefjord, Camilla. "Th1, Th2 and Treg associated factors in relation to allergy". Doctoral thesis, Linköping : Linköpings universitet, 2006. http://www.bibl.liu.se/liupubl/disp/disp2006/med947s.pdf.
Testo completo
43
Wan, Kong-Sang. "Regulation of lung Th1 and Th2 CD4'+T cell responses". Thesis, University of Southampton, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.390720.
Testo completo
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Bruchard, Mélanie. "Etude de NLRP3 dans les cellules myéloïdes immunosuppressives et les lymphocytes TCD4 dans un contexte de cancer". Thesis, Dijon, 2013. http://www.theses.fr/2013DIJOS030/document.
Testo completoAbstract (sommario):
L’inflammasome NLRP3 est un complexe multiprotéique responsable notamment de la production d’IL-1β, une cytokine inflammatoire. Les effets délétères de l’inflammasome NLRP3 ont été démontrés dans de nombreuses maladies dont le cancer. Ce travail se concentre sur les effets de NLRP3 dans le contexte du cancer.Dans un premier projet, j’ai étudié l’activation de l’inflammasome NLRP3 dans les MSDC après un traitement par chimiothérapie. Deux chimiothérapies, le 5-Fluorouracile et la Gemcitabine, sont capables d’éliminer de façon spécifique les MDSC, population de cellules immunosuppressives dont la taille augmente en cas de cancer. J’ai découvert que le 5-Fluorouracile et la Gemcitabine activaient l’inflammasome NLRP3 dans les MDSC. En effet, le 5-Fluorouracile et la Gemcitabine provoquent la perméabilisation du lysosome des MDSC, permettant la sortie de la cathepsine B, protéine lysosomale, dans le cytoplasme où elle interagit directement avec NLRP3. Cette interaction active l’inflammasome NLRP3 et la production d’IL-1β. Cette IL-1β est responsable du développement d’une nouvelle population immunosuppressive, les Th17.J’ai ensuite étudié le rôle de NLRP3 dans la différenciation des lymphocytes T CD4 Th2. Dans ces cellules, le rôle de NLRP3 s’effectue indépendamment du reste du complexe multiprotéique qui forme l’inflammasome. Après avoir été induit par la cascade de signalisation de l’IL-2, NLRP3 interagit avec IRF4 (interferon regulatory factor) et agit comme un facteur de transcription sur le promoteur du gène de l’IL-4. L’absence de NLRP3 a pour conséquence une production moins importante d’IL-4 par les Th2 qui sont alors moins fonctionnelsThe inflammasome NLRP3 (NOD like receptor pyd containing 3) is a multiprotein complex notably responsible for IL-1β (interleukine-1β) production, an inflammatory cytokine. Negative effects have been observed in various diseases including cancer. My thesis focuses on the effects of NLRP3 in cancer.In my first project, I studied the NLRP3 inflammasome activation in MDSC (myeloïd derived suppressor cells) after a chemotherapy treatment. Two chemotherapies, 5-Fluorouracil and Gemcitabine, are selectively able to kill MDSC, an immunosuppressive population growing during cancer evolution. MDSC’s death restores anti-tumor immunity for a while but another immunosuppressive population is established by MDSC produced IL-1β before their disappearance. I discovered that 5-Fluorouracil and Gemcitabine trigger NLRP3 inflammasome activation in MDSC. 5-Fluorouracil and Gemcitabine induce lysosomal permeabilisation, allowing for Cathepsin B release into the cytoplasm where it directly interacts with NLRP3. That interaction activates the inflammasome and induces IL-1β production which is responsible for the development of another immunosuppressive population, called Th17 cells.I then studied the role of NLRP3 during Th2 differentiation. Here, NLRP3 actions are done independently of the other inflammasome forming proteins. After being induced by IL-2 signalization pathway, NLRP3 interacts with IRF4 (interferon regulatory factor 4) and acts as a transcription factor on the IL-4 promoter gene. Lack of NLRP3 leads to a smaller IL-4 production by Th2 cells which are consequently less functional
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Liddiard, Kate. "Macrophage Th2 cytokine-indiced gene expression in atherosclerosis". Thesis, University of Oxford, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.289266.
Testo completo
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Nickdel, Mohammad Barat. "Role of Th2 cytokines in Toxoplasma gondii infection". Thesis, University of Strathclyde, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.248258.
Testo completo
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Xiong, Ye. "KLF2: A Kruppel like Family Transcription Factor in Myeloid Cells Negatively Regulates Th2 Response". University of Cincinnati / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1445343045.
Testo completo
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Piehler, Daniel. "The inflammatory response against Cryptococcus neoformans is regulated by eosinophilic granulocytes and the interleukin-4/interleukin-4 receptor axis". Doctoral thesis, Universitätsbibliothek Leipzig, 2011. http://nbn-resolving.de/urn:nbn:de:bsz:15-qucosa-78248.
Testo completoAbstract (sommario):
Cytokines play an important regulatory role during immune responses against pathogens. The outcome of an induced cytokine pattern is determined by many factors. It strongly depends on the nature of the pathogen and the host’s ability to control the quality and strength of cytokine signals. In pulmonary infection with Cryptococcus neoformans T helper (Th) 1 and Th17 cell subsets and their associated cytokines confer protection, whereas a Th2-biased response with production of interleukin (IL) -4 confers susceptibility. Since inappropriate Th responses often lead to death in immunosuppressed human patients, especially HIV-1 infected patients, this work aimed to elucidate mechanisms of Th2 induction and regulation by assessing the Th2 hallmark cytokine IL-4 in an experimental model of cryptococcosis. Therefore, a kinetic study of IL-4 expression during 70 days after intranasal infection was performed in susceptible mice. The analyses included characterization of pulmonary leukocytes and Th cell cytokine profiling. IL-4 profiling revealed Cryptococcus-specific IL-4 production not before six weeks after infection. This unexpected finding was further validated by equal results observed in a kinetic study done in IL-4 reporter mice. These mice express a green fluorescent protein simultaneously to IL-4 expression in the same cell and this protein can be detected by flow cytometry. Two cellular sources of IL-4 were identified: Th2 cells were found as expected, but also, as shown for the first time, eosinophilic granulocytes could be demonstrated to secrete IL-4.
Next, the influence of eosinophils on pulmonary inflammation and disease development was investigated using ΔdblGATA-1 mice constitutively devoid of eosinophilic granulocytes. Experiments with infected ΔdblGATA-1 mice revealed novel regulatory functions of eosinophils in cryptococcosis. In the absence of eosinophils pulmonary Th cell recruitment was significantly diminished. In addition, Th2 polarization was reduced in ΔdblGATA-1 mice as shown by reduced numbers of Th2 cells expressing the Th2-related surface marker T1/ST2 and reduced albeit not absent IL-4 production by Th cells. In addition to reduced IL-4 production, in the absence of eosinophils Th cells with enhanced interferon-γ and IL-17 production were observed. However, control of pulmonary fungal growth was only slightly enhanced in the absence of eosinophils and dissemination of cryptococci to the brain was unaltered. This may be related to the shared IL-4 production by not only eosinophils but also Th2 cells. Blocking more than one cellular source of IL-4 could be required to prevent immunopathology.
To test the hypothesis of gradual IL-4-dependent immunopathology, experiments were conducted using mice expressing only one allele of the IL-4receptor (R) alpha (α) chain (+/-) instead of two (+/+). Indeed, mono-allelic expression of the IL-4Rα resulted in an intermediate expression of the IL-4R on the surface of myeloid and lymphoid cells indicating a gene-dosage effect for IL-4R expression. Infected IL-4Rα+/- mice displayed reduced susceptibility as compared with IL-4Rα+/+ mice, and IL-4Rα-/- mice completely lacking IL-4R expression were found to be protected with survival for the complete time period of the experiment (i.e. up to 275 days). Reduced susceptibility found in infected IL-4Rα+/- mice was associated with decreased serum levels of immunoglobulin E, reduced mucus production by airway epithelia, attenuation of airway hyper-reactivity, and reduced formation of alternatively activated macrophages in lung parenchyma – pathophysiological features, which are typically found in experimental models of asthma but also in asthma of humans and animals. Since no up-regulation of IL-4R by the infection with Cryptococcus neoformans was found, the experimental pulmonary infection model used appears to be a very sensitive low-level IL-4 system. This work highlights the outstanding role of IL-4 and its different cellular sources as well as its receptor in cryptococcosis and provides novel insights into pathogenesis. Moreover, a cellular (i.e. eosinophils) and a molecular (i.e. IL-4R) target for treatment of this mycosis and possibly of asthma is provided.
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Pereira, Leonardo Biscaro. "Avaliação do perfil de citocinas no tecido subcutâneo de camundongos na presença de cimento endodôntico". Universidade de São Paulo, 2013. http://www.teses.usp.br/teses/disponiveis/58/58135/tde-03102013-151254/.
Testo completoAbstract (sommario):
Avaliou-se a capacidade dos cimentos endodônticos: Sealapex®, Activ-GP® e AH-Plus® de alterarem o perfil das citocinas nas respostas Th1, Th2 e Th17, após a implantação destes em subcutâneo de camundongos. A quantificação das citocinas IL-2, IL-6, TNF-α, IFN-γ, IL-4, IL-10 e IL-17 foi realizada in vivo, no tecido reacional circundante aos implantes, os quais foram confeccionados a partir de sondas nasogástricas estéreis e apirogênicas de cloreto de polivinila preenchidas com os cimentos, tendo um grupo controle com sondas vazias. Utilizou-se camundongos isogênicos da linhagem C57BL/6 machos de 6/8 semanas de vida sendo que cada um recebeu 2 implantes na região dorsal (lado direito e esquerdo). Após os períodos experimentais de 7, 21 e 63 dias, com os camundongos anestesiados, os implantes foram removidos juntamente com o tecido circundante, e os animais sacrificados em seguida por deslocamento cervical. As amostras de cada grupo foram divididas sendo: duas, contendo implante/tecido, processadas histotecnicamente e as demais com apenas tecido (sem implante) foram homogeneizadas e centrifugadas com solução formada por tampão RIPA e inibidor de protease. O sobrenadante, fruto deste processo, foi coletado e a dosagem das citocinas realizada através do kit CBA mouse-Th1/Th2/Th17 Cytokine Kit (BD Cytometric Bead Array, San Jose, CA, USA) em análise por citometria de fluxo. Os parâmetros avaliados foram a concentração da citocina em função do cimento testado em cada período experimental. Submeteu-se os resultados à análise estatística por meio do teste t com a correção de Welch\'s. Para todos os testes o nível de significância foi de 5%. Com relação à IL-2 houve diferenças estatísticas significantes entre os grupos Activ-GP® e AH-Plus® (p=0,0391). No período de 21 dias foram detectadas diferenças entre o grupo controle e AH-Plus® (p=0,0402) e entre o grupo Sealapex® e AH-Plus® (p=0,0244). O AH-Plus® induziou um maior aumento na IL-6, aos 7 dias em relação ao Activ-GP® (p=0,0286) e aos 21 dias entre o grupo controle (p=0.0402) e Activ-GP® (p=0.0244). Os níveis de TNF-α foram estatisticamente superiores após 7 dias quando comparou-se o grupo AH-Plus® com os demais. Observou-se que no grupo controle aos 7 e 21 dias ocorreram diferenças estatísticas em relação ao Sealapex® e AH-Plus® respectivamente quando avaliadas as concentrações de IFN-γ. Houve também diferenças estatísticas entre o grupo controle e Sealapex® (p=0,0158) no período de 7 dias para a citocina IL-4. Os valores de IL-10 foram estatisticamente superiores para o grupo controle em relação ao Activ-GP® no período de 21 dias (p=0,0471). Com relação a IL-17 no período de 21 dias, observou-se os maiores valores para o grupo controle, seguido pelo Sealapex®, Activ-GP® e AH-Plus®. Foram detectadas diferenças entre os grupos controle e AH-Plus® (p=0,0121), controle e Activ-GP® (p=0,0262) e entre Sealapex® e Activ GP® (p=0,0314). Baseado nesses resultados podê-se concluir que: os cimentos endodônticos são capazes de modular as respostas Th1, Th2 e Th17 através da inibição ou estimulação da liberação das citocinas testadas. O cimento AH-Plus® promoveu as maiores diferenças no perfil de resposta Th1.It was evaluated the capacity of the following endodontic sealers: Sealapex, Activ-GP and AH-Plus to modify the cytokine profile in Th1, Th2 and Th17 responses, after their implantation in the subcutaneous tissue of mice. Quantification of IL-2, IL-6, TNF-α, IFN-γ, IL-4, IL-10 and IL-17 was performed in vivo, in the reactional tissue surrounding the implants, which were made from sterile nasogastric probes and apyrogenic of polyvinyl chloride filled with sealer, and a control group of empty probes. It was used isogenic mice of C57BL/6 lineage, 6/8 weeks old males, each of which received two implants in the dorsal region (left and right). After the experimental time of 7, 21 and 63 days, the mice were anesthetized and the implants were removed along with the surrounding tissue, the animals were then sacrificed by cervical dislocation. Samples from each group were divided as follows: two containing implant / tissue processed histologically and with only the remaining tissue (without implant) were mixed and centrifuged with a solution formed by RIPA buffer and protease inhibitors. The supernatant result of this process was collected and cytokine dosage accomplished by mouse-Th1/Th2/Th17 Cytokine CBA Kit Kit (BD cytometric Bead Array, San Jose, CA, USA) for flow cytometry analysis. The evaluated parameters were the cytokine concentration in function of sealer tested in each trial. The results were submitted to statistical analysis using the t test with Welch\'s correction. For all tests the significance level was 5%. With respect to IL-2 there were significant statistical differences between groups-Activ GP and AH-Plus (p=0.0391). In the period of 21 days differences were found between the control group and AH-Plus (p=0.0402) and between the group Sealapex and AH-Plus (p=0.0244). The AH-Plus induced a greater increase in IL-6, at 7 days compared to Activ-GP (p=0.0286) and at 21 days between the control group (p=0.0402) and Activ-GP (p=0.0244). The levels of TNF-α were significantly higher after 7 days when the AH-Plus group was compared with others. It was observed that in the control group at 7 and 21 days there were statistical differences in relation to Sealapex and AH-Plus respectively when evaluated concentrations of IFN-γ. There were also significant differences between the control group and Sealapex (p=0.0158) within 7 days for the cytokine IL-4. The amounts of IL-10 were statistically higher in the control group compared to the Activ GP in a period of 21 days (p=0.0471). With respect to IL-17 in a period of 21 days, it was observed the highest values for the control group, followed by Sealapex, Activ-GP and AH-Plus. Differences were found between the control groups and AH-Plus (p=0.0121), control and Activ-GP (p=0.0262) and between Sealapex and Activ-GP (p=0.0314). Based on the presented results theendodontic sealers are able to promote changes in the response cytokine profile Th1, Th2 and Th17; Sealer AH-Plus produced the greatest changes, in the Th1 response profile.
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Gimsa, Ulrike. "T-Zell-vermittelte Autoimmunität". Doctoral thesis, Humboldt-Universität zu Berlin, Medizinische Fakultät - Universitätsklinikum Charité, 2004. http://dx.doi.org/10.18452/13903.
Testo completoAbstract (sommario):
Die vorliegende Arbeit befaßt sich mit T-Helferzellen und ihren Interaktionen mit Gewebszellen, wie sie im gesunden Organismus und in Autoimmunerkrankungen auftreten. Es werden Fragen der Toleranzinduktion durch orale Gabe von Antigenen, speziell der oralen Verabreichung von Collagen II bei Patienten mit rheumatoider Arthritis diskutiert. Eine Immundeviation als Mittel, inflammatorische Th1-Zellantworten in anti-inflammatorische Th2-Zellantworten zu verwandeln, kann durch Eingriffe in die T-Zell-Signaltransduktion erreicht werden. Es werden neue Ansätze zu Mechanismen diskutiert, die das Immunprivileg des Zentralnervensystems gewährleisten. Die hirnresidenten Immunzellen, zu denen Mikrogliazellen und Astrozyten zählen, besitzen Eigenschaften, die eine Entzündung unwahrscheinlich machen. Sie müssen aktiviert werden, um Antigene präsentieren zu können. In organtypischen entorhinal-hippocampalen Schnittkulturen konnte gezeigt werden, dass Mikrogliazellen durch Th1-Zellen aktiviert, von Th2-Zellen hingegen deaktiviert werden. Die Möglichkeit, dass die Costimulation über CD80 oder CD86 differentielle Effekte auf den Charakter der Immunantwort hat, wird diskutiert. Der Einfluß von pro-inflammatorischen Zytokinen auf Mikrogliaaktivierung und den Erhalt von Nervenfasern wurde ebenfalls in Hirnschnittkulturen untersucht. Astrozyten sind wesentlicher Bestandteil der Blut-Hirn-Schranke. Diese kann jedoch von aktivierten T-Zellen überwunden werden. In dieser Arbeit wird gezeigt, dass Astrozyten über eine Expression von CD95L in aktivierten T-Zellen Apoptose induzieren können. Davon sind jedoch nicht alle T-Zellen betroffen. Andererseits wird eine T-Zellproliferation unterdrückt, indem T-Zellen unter Astrozyteneinfluß verstärkt CTLA-4 exprimieren, was einen Zellzyklusarrest zur Folge hat. Darüber hinaus ist eine verstärkte Produktion von Nervenwachstumfaktor (NGF; nerve growth factor) nach antigenspezifischer Interaktion von Astrozyten mit Th1- und Th2-Zellen als zusätzliches Mittel, eine Neuroinflammation einzudämmen, anzusehen. Die Arbeit stellt diese Ergebnisse in fünf Kapiteln dar, welche gleichzeitig eine Einführung in die als Anlagen enthaltenen zehn Publikationen geben.This thesis deals with T helper cells and their interactions with tissue cells as they occur in the healthy organism and in autoimmune diseases. Questions of tolerance induction by oral application of antigens are discussed especially oral treatment with type II collagen in patients with rheumatoid arthritis. In order to transform inflammatory Th1 responses into anti-inflammatory Th2 responses, immune deviation can be reached by interference with T-cell signal transduction. New approaches towards the different ways that the immune privilege of the central nervous system is maintained are discussed. The resident immune cells, i.e. microglia and astrocytes possess properties that make inflammation unlikely. They have to be activated in order to present antigens. It has been shown in organotypic entorhinal-hippocampal slice cultures that Th1 cells activate whereas Th2 cells deactivate microglial cells. The possibility is discussed as to whether costimulation via CD80 or CD86 differentially influences the character of the immune response. The influence of pro-inflammatory cytokines on microglial activation and preservation of nerve fibers has also been studied in brain slice cultures. Astrocytes are an essential part of the blood-brain barrier, which can be crossed by activated T cells. The thesis shows that astrocytes can induce apoptosis in activated T cells via expression of CD95L. However, not all T cells are affected. T cell proliferation is suppressed by increased CTLA-4 expression in T cells under the influence of astrocytes, resulting in a cell cycle arrest. An additional mechanism of confining neuroinflammation is increased production of the nerve growth factor (NGF) following antigen-specific interaction of astrocytes and Th1 and Th2 cells, respectively. These results are presented in five chapters that also introduce the ten attached publications.