Littérature scientifique sur le sujet « T-cell subpopulations »
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Articles de revues sur le sujet "T-cell subpopulations"
Tian, Yamin, Seiichiro Kobayashi, Nobuhiro Ohno, Masamichi Isobe, Mayuko Tsuda, Yuji Zaike, Nobukazu Watanabe, Kenzaburo Tani, Arinobu Tojo et Kaoru Uchimaru. « Leukemic T Cells Are Specifically Enriched In a Unique CD3dimCD7low Subpopulation of CD4+ T Cells In Acute-Type Adult T Cell Leukemia ». Blood 116, no 21 (19 novembre 2010) : 4144. http://dx.doi.org/10.1182/blood.v116.21.4144.4144.
Texte intégralPhillips, S. M., D. Walker, S. K. Abdel-Hafez, G. P. Linette, B. L. Doughty, P. J. Perrin et N. el Fathelbab. « The immune response to Schistosoma mansoni infections in inbred rats. VI. Regulation by T cell subpopulations. » Journal of Immunology 139, no 8 (15 octobre 1987) : 2781–87. http://dx.doi.org/10.4049/jimmunol.139.8.2781.
Texte intégralKanof, Marjorie E. « Purification of T Cell Subpopulations ». Current Protocols in Immunology 00, no 1 (décembre 1991) : 7.3.1–7.3.5. http://dx.doi.org/10.1002/0471142735.im0703s00.
Texte intégralKubick, Norwin, Patrick C. Henckell Flournoy, Ana-Maria Enciu, Gina Manda et Michel-Edwar Mickael. « Drugs Modulating CD4+ T Cells Blood–Brain Barrier Interaction in Alzheimer’s Disease ». Pharmaceutics 12, no 9 (16 septembre 2020) : 880. http://dx.doi.org/10.3390/pharmaceutics12090880.
Texte intégralLeonhardt, U., U. Wagner, M. Werner et L. Engelmann. « T-cell-subpopulations in septic patients ». Critical Care 5, Suppl 1 (2001) : P059. http://dx.doi.org/10.1186/cc1127.
Texte intégralFerrara, Andrea, Marvin M. McMillen et Garth H. Ballantyne. « T-cell subpopulations and colorectal cancer ». Diseases of the Colon & ; Rectum 33, no 5 (mai 1990) : 367–69. http://dx.doi.org/10.1007/bf02156259.
Texte intégralAbramova, A. V., I. V. Galtseva, E. A. Mikhailova, N. M. Kapranov, Yu O. Davydova, Z. T. Fidarova, V. V. Troitskaya, E. N. Parovichnikova et V. G. Savchenko. « Oligoclonality and subpopulation structure of bone marrow T-cells in patients with aplastic anaemia ». Russian journal of hematology and transfusiology 65, no 4 (10 décembre 2020) : 417–30. http://dx.doi.org/10.35754/0234-5730-2020-65-4-417-430.
Texte intégralHafler, D. A., D. A. Fox, D. Benjamin et H. L. Weiner. « Antigen reactive memory T cells are defined by Ta1. » Journal of Immunology 137, no 2 (15 juillet 1986) : 414–18. http://dx.doi.org/10.4049/jimmunol.137.2.414.
Texte intégralSKÖLD, RYTTER, IVARS et CARDELL. « Characterization of Subpopulations of T-Cell Receptor Intermediate (TCRint) T Cells ». Scandinavian Journal of Immunology 49, no 6 (juin 1999) : 611–19. http://dx.doi.org/10.1046/j.1365-3083.1999.00535.x.
Texte intégralBertrand, F. E., L. G. Billips, G. L. Gartland, H. Kubagawa et H. W. Schroeder. « The J chain gene is transcribed during B and T lymphopoiesis in humans. » Journal of Immunology 156, no 11 (1 juin 1996) : 4240–44. http://dx.doi.org/10.4049/jimmunol.156.11.4240.
Texte intégralThèses sur le sujet "T-cell subpopulations"
McKnight, Andrew John. « The repertoire of lymphokine production by T cell subpopulations ». Thesis, University of Oxford, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.291402.
Texte intégralTormey, Vincent Joseph. « Regulation of macrophage subpopulations and their relationship to T-cell function in the pathogenesis of asthma ». Thesis, University College London (University of London), 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.367893.
Texte intégralRogers, Paul R. « Analysis of CD45 Alternative Exon Expression in Murine and Human CD4+ T Cell Subpopulations : a Thesis ». eScholarship@UMMS, 1993. http://escholarship.umassmed.edu/gsbs_diss/282.
Texte intégralRädler, Diana [Verfasser], et Thomas [Akademischer Betreuer] Illig. « Mechanisms of immune regulation during development of atopic diseases in childhood : analysis of T cell subpopulations considering genetic and epigenetic influences / Diana Rädler. Betreuer : Thomas Illig ». München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2014. http://d-nb.info/104915312X/34.
Texte intégralJiang, Janina Q. « The production of HIV suppressive factors by CD28, CD38 and HLA-DR subpopulations of CD8+ T cells ». Thesis, University of Ottawa (Canada), 2001. http://hdl.handle.net/10393/9104.
Texte intégralMourah, Fadila. « Caractérisation phénotypique et fonctionnelle des sous-populations de monocytes dans les réponses immunitaires ». Thesis, Sorbonne Paris Cité, 2017. http://www.theses.fr/2017USPCC319/document.
Texte intégralMonocytes are circulating leukocytes which characterization has long been difficult. Dissection of these cells into functional subpopulations in humans is still insufficient. Monocytes are however circulating precursors of several populations of dendritic cells and tissue macrophages, and play a prominent role in the development of immune response in steady state and pathology. At present, three monocyte subpopulations are described in humans: classical CD14+CD16neg, non-classical CD14dimCD16+ and intermediates CD14++CD16. Functionally, these subpopulations are diverse and heterogeneous and with apparently redundant pro - and anti-inflammatory properties. In pathology, an increase in the ratio of CD16 + to CD16neg monocytes has been described in inflammatory situation, suggesting a role of the former in the development and amplification of inflammation. Among the non-classical monocytes, cells that can detect changes in the endothelium and having then specific properties of vascular bed monitoring have been identified and characterized. In order to get a better definition of monocyte populations and break them down into subpopulations in which the identification of the cell functions would be more accessible, I endeavoured in this thesis work to analyse different populations of circulating human monocytes as comprehensively as possible and with state of the art analytical and computer tools. The results of flow cytometry analysis of PBMC from 28 healthy donors after cell staining with twenty antibodies directed against surface molecules revealed the existence of a population of monocytes of larger size
Cohen, Shannon. « Identification et caractérisation fonctionnelle de sous-populations monocytaires circulantes chez l'homme ». Thesis, Sorbonne Paris Cité, 2018. http://www.theses.fr/2018USPCC241.
Texte intégralMonocytes are circulating leucocytes, precursors of dendritic cells and macrophages, whose phenotype is heterogeneous. The association between human monocyte subsets described in the literature and the functions in the immune response remains difficult.The different populations of human monocytes are classified according to the expression of surface markers CD14 and CD16. Three populations have thus been identified: the classical monocytes CD14+ CD16neg, the non-classical monocytes CD14dim CD16+ and the intermediate monocytes CD14+ CD16+. The functions assigned to these populations are diverse and entangled. In particular, the pro- and anti-inflammatory properties associated with these populations are redundant and conflicting depending on the authors. In an inflammatory situation, the increase of the CD16+ monocyte fraction suggests their involvement in the development and/or the amplification of inflammation.The aim of this thesis is to improve the definition of monocytes populations so that they can be subdivided into subpopulations whose functions are better defined. This work was part of a long term laboratory project which has the goal to the most comprehensive phenotypic analysis of monocytes, using current biological and computer analysis tools. This highlighted to demonstrate the existence of a larger monocyte population. These "large" monocytes are subdivided into CD16neg and CD16+ populations (respectively named la14+16neg and la14+16+). Monocytes commonly analyzed, of smaller size or "small", are subdivided as expected in three subpopulations identified here as monocytes sm14+16neg largely in the majority, sm14dim16+ and sm14+16+.Finally, the analysis of the phenotypes of circulating monocytes in pathological situation was conducted in burn victims. These patients have an increased susceptibility to infection due, among other things, to deficient innate immune responses. These results obtained in 18 patients taken at admission and at 7 and 28 days later permitted to identify different phenotypic modification profiles of monocytes and their evolution depending on the clinical state. This study has also highlighted the existence of a population of cells with high granulosity, greatly amplified in patients and whose functions are being analyzed
Blanc, Charlotte. « Lymphocytes T résidents mémoires dans les tumeurs du poumon et ORL : sous-populations et mécanismes de migration Cxcr6-deficiency impairs cancer vaccine efficacy and resident memory CD8+ T cells recruitment in tumor Phénotype et localisation des sous-populations de LT résidents mémoires dans les tumeurs pulmonaires ». Thesis, Sorbonne Paris Cité, 2019. http://www.theses.fr/2019USPCB046.
Texte intégralWith the immunoediting theory, new concept in the cancer physiopathology has appeared in the beginning of the 21st century. It is now established that the immune system and CD8+ T cells play a crucial role in tumor growth control. However, by selective pressure, the tumor cell develops mechanisms to avoid immune destruction and to inhibit T cells cytotoxicity. Reinvigorating antitumor functions is a well-proven therapeutic strategy with immunotherapy. Nevertheless, patients do not always respond to these treatments which could be optimized. In this context, we had studied antitumor response induction by focusing on CD8+ T cells and especially on resident memory T cells (Trm), new cytotoxic cells correlated with a good prognosis and which could be a relevant therapeutic target. A potent antitumor response requires an optimal antigenic presentation to prime CD8+ T cells and favor their migration into the tumor through chemokine network. In a first study, we identified a chemokine receptor CXCR6, highly expressed by lung CD8+ Trm. Its chemokine CXCL16 is produced by antigen presenting cells, epithelial and tumor cells, but the role of the CXCR6/CXCL16 axis in cancer immunosurveillance is not known yet. To understand its mechanisms, antitumor vaccinations strategies by intranasal (i.n.) route had been set up in CXCR6-deficient mice and had shown the role of CXCR6 in promoting the infiltration of specific CD8+ T cells and Trm in lung tissue and head and neck tumors. The CXCR6/CXCL16 axis could represent an interesting therapeutic tool for antitumor vaccines or adoptive cell transfer in which tumor infiltration is a challenge. Trm have the particularity to express integrins (CD103, CD49a) involved in the interaction with the tumor microenvironment. They exhibit an original and an heterogenous phenotype, microenvironment-dependent. Their phenotype is involved in their cytotoxic activities, highlighting their high prognostic impact and their potential to be a suitable therapeutic target. Better understanding Trm phenotype complexity and their induction mechanisms are crucial to further optimize antitumor response. The second work of this thesis focused on the expression of two main integrins CD103 and CD49a in lung cancer by an in situ multiparametric immunofluorescence technique and by flow cytometry. The results showed that their expression determine their contact with the tumor cells and their involvement in patient survival. Our data obtained by i.n. vaccination models and by tertiary lymphoid structures analysis suggest the possibility of a priming in the lung to induce the Trm phenotype. Our work shows the necessity of analyzing local immunity and CD8+ Trm T cells for a better understanding of antitumor response. Studying Trm phenotype has highlighted their crucial role and their potential to be a relevant therapeutic target. Identifying and targeting their mechanisms of induction might optimize therapies and patient's survival
Qian, Chongsheng. « Immunothérapie adoptive pour le traitement des infections à Adénovirus réfractaires après allogreffes de Cellules Souches Hématopoïétiques : de la recherche fondamentale à la recherche clinique ». Thesis, Université de Lorraine, 2017. http://www.theses.fr/2017LORR0069/document.
Texte intégralHematopoietic stem cell transplantation (HSCT) is one of the only curative treatments for benign or malignant hematological diseases and primary immune deficiencies. However, viral infections and graft-versus-host disease (GVHD) are among the most frequent complications after HSCT associated with high morbidity and mortality. Viral infections often occur in the absence of specific immune reconstitution in the context of immunosuppression related to GVHD itself or to the prophylaxis or treatment of GVHD. The recommended anti-viral drug treatments have an inconsistent efficacy in this context of immunodeficiency and are not devoid of toxicity. The promising therapeutic alternative is adoptive immunotherapy, in particular the infusion of specific anti-viral T lymphocytes isolated by immunomagnetic technique (VSTs). However, these T lymphocytes may be targeted by immunosuppressive treatments administered for GVHD, but also may be the cause of the onset or reactivation of GVHD. We have shown in this work that the efficacy of VSTs, which is based on their in vivo expansion when they encounter the circulating virus, is mainly allowed by the most immature lymphocyte subpopulations, even in a small proportion. We argue in this work that the efficacy of VSTs and their persistence is mainly based on the presence of the most immature T lymphocyte subpopulations and this regardless of the degree of HLA compatibility between the VSTs and the recipient. Moreover, their moderate sensitivity to corticosteroids, which we have studied in vitro, does not justify the modulation of immunosuppression at the time of infusion of ADV-VSTs, as observed in vivo in the multicenter phase I / II clinical trial we conducted between 2012 and 2015. Indeed, this clinical trial does not report any de novo GVHD after ADV-VSTs infusion. On the other hand, modulation of immunosuppression may potentially be incriminated in the reactivation of GVHD within weeks of ADV-VST infusion. A Phase II comparative trial will bring the evidence of efficacy and will clearly determine the role of VSTs in the reactivation of GVHD
Cohen-Kaminsky, Sylvia. « Analyse de composants cellulaires et moleculaires du microenvironnement thymique chez l'homme : interet dans l'etude du role du thymus dans la myasthenie ». Paris 6, 1988. http://www.theses.fr/1988PA066157.
Texte intégralLivres sur le sujet "T-cell subpopulations"
Ian, Kimber, et Selgrade MaryJane K, dir. T lymphocyte subpopulations in immunotoxicology. Chichester : John Wiley & Sons, 1998.
Trouver le texte intégralT-helper cell subpopulations. Copenhagen : Munksgaard, 1991.
Trouver le texte intégralKimber, Ian, et MaryJane K. Selgrade. T Lymphocytes Subpopulations in Immunotoxicology. Wiley & Sons, Incorporated, John, 2007.
Trouver le texte intégralKisor, Robin L. A quantitative and functional analysis of T Lymphocyte subpopulations in protein and/or zinc deficient mice. 1988.
Trouver le texte intégralChapitres de livres sur le sujet "T-cell subpopulations"
Romagnani, Sergio. « T Cell Subpopulations ». Dans History of Allergy, 155–64. Basel : S. KARGER AG, 2014. http://dx.doi.org/10.1159/000358622.
Texte intégralOhigashi, Izumi, et Yousuke Takahama. « Flow Cytometry Analysis of Thymic Epithelial Cells and Their Subpopulations ». Dans T-Cell Development, 65–73. New York, NY : Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-2809-5_5.
Texte intégralKatz, J., J. H. Eldridge et S. M. Michalek. « Rat T cell subpopulations : Effect of environmental and microbial antigens ». Dans Advances in Mucosal Immunology, 186–87. Dordrecht : Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-1848-1_53.
Texte intégralClement, Loran T., Max D. Cooper et Thomas F. Tedder. « Analysis of the Ontogeny and Function of Human Helper T Cell Subpopulations ». Dans Leukocyte Typing II, 101–9. New York, NY : Springer New York, 1986. http://dx.doi.org/10.1007/978-1-4613-8587-5_8.
Texte intégralCalvano, S. E., J. D. Albert, A. Legaspi, B. Organ, K. J. Tracey, S. F. Lowry, G. T. Shires et A. C. Antonacci. « T Cell Subpopulations Following Thermal Injury Effect of the Acute Stress Response ». Dans Lipid Mediators in the Immunology of Shock, 349–60. Boston, MA : Springer US, 1987. http://dx.doi.org/10.1007/978-1-4613-0919-2_38.
Texte intégralBottomly, K., M. Luqman, J. Murray, J. West, A. Woods et S. Carding. « Clonal Expansion and Differentiation to Effector Function in Normal CD4 T Cell Subpopulations ». Dans Progress in Immunology, 593–97. Berlin, Heidelberg : Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-83755-5_80.
Texte intégralMinskaia, Ekaterina, et João F. Lacerda. « Analysis of FOXP3 DNA Methylation Patterns to Identify Functional FOXP3+ T-Cell Subpopulations ». Dans Methods in Molecular Biology, 115–36. New York, NY : Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2647-4_9.
Texte intégralBarrett, Douglas J., Desmond A. Schatz et John W. Sleasman. « Immunoregulatory CD4+ T Cell Subpopulations : Enumeration, Activation, and Functional Analyses in Normals and Autoimmune Disease ». Dans Topics in Pediatrics, 83–95. New York, NY : Springer New York, 1990. http://dx.doi.org/10.1007/978-1-4612-3230-8_8.
Texte intégralKronin, Vadim, Gabriele Süss, Ken Winkel et Ken Shortman. « The Regulation of T Cell Responses by a Subpopulation of CD8+DEC205+ Murine Dendritic Cells ». Dans Advances in Experimental Medicine and Biology, 239–48. Boston, MA : Springer US, 1997. http://dx.doi.org/10.1007/978-1-4757-9966-8_40.
Texte intégralMami-Choubaid, F., et T. Hercend. « TCT.1 : A Target Structure for a Subpopulation of Human γ/δ T Lymphocytes ». Dans Function and Specificity of γ/δ T Cells, 189–95. Berlin, Heidelberg : Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-642-76492-9_26.
Texte intégralActes de conférences sur le sujet "T-cell subpopulations"
Nakstad, Britt, et Torstein Lyberg. « PR0C0AGULANT ACTIVITIES IN HUMAN ALVEOLAR MACROPHAGES : ». Dans XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643159.
Texte intégralChen, Gregory M., Changya Chen, Rajat K. Das, Yang-Yang Ding, Bing He, Hannah Kim, David M. Barrett et Kai Tan. « Abstract PR3 : Development of a transcriptomic T-cell atlas highlights the differential role of T-cell subpopulations in CAR T-cell therapy resistance ». Dans Abstracts : AACR Special Conference on Tumor Immunology and Immunotherapy ; November 17-20, 2019 ; Boston, MA. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/2326-6074.tumimm19-pr3.
Texte intégralPinho, Mariana Pereira, et José Alexandre Marzagão Barbuto. « Abstract B069 : Systemic alterations in T cell subpopulations of breast cancer patients ». Dans Abstracts : CRI-CIMT-EATI-AACR Inaugural International Cancer Immunotherapy Conference : Translating Science into Survival ; September 16-19, 2015 ; New York, NY. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/2326-6074.cricimteatiaacr15-b069.
Texte intégralDi Sante, G., M. C. Caparello, B. Tolusso, C. Di Mario, M. Valentini, F. Ria, G. Ferraccioli, R. Cimaz et E. Gremese. « FRI0002 Analysis of b cells and t cells subpopulations and collagen specific t cell repertoire in juvenile idiopathic arthritis patients ». Dans Annual European Congress of Rheumatology, EULAR 2018, Amsterdam, 13–16 June 2018. BMJ Publishing Group Ltd and European League Against Rheumatism, 2018. http://dx.doi.org/10.1136/annrheumdis-2018-eular.5415.
Texte intégralSaito, Takuro, Hiroyoshi Nishikawa, Hisashi Wada, Masaki Mori, Yuichiro Doki et Shimon Sakaguchi. « Abstract B174 : FOXP3+CD4+ T-cell subpopulations distinctly control the prognosis of colorectal cancers ». Dans Abstracts : CRI-CIMT-EATI-AACR Inaugural International Cancer Immunotherapy Conference : Translating Science into Survival ; September 16-19, 2015 ; New York, NY. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/2326-6074.cricimteatiaacr15-b174.
Texte intégralDyhre-Petersen, Nanna, Gustav Ørting Jørgensen, Louise Munkholm Andreasson, Trine Hilkjær Petersen, Lisa Pfluger, Alexander Wessely Silberbrandt, Morten Winther Hvidtfeldt, Charlotte Menne Bonefeld, Celeste Porsbjerg et Asger Sverrild. « Effects of blocking TSLP on ILC and T cell subpopulations in patients with asthma ». Dans ERS Lung Science Conference 2022 abstracts. European Respiratory Society, 2022. http://dx.doi.org/10.1183/23120541.lsc-2022.94.
Texte intégralKoller, U., I. Pabinger, K. Lechner et W. Knapp. « HEAT INACTIVATED HIGHLY PURIFIED FACTOR VIII CONCENTRATE IN THE TREATMENT OF HEMOPHILIACS ». Dans XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644057.
Texte intégralXu, Qing, BaiHua Cheng et Songlin Xu. « Effects of diode laser ILIB on peripheral blood T lymphocyte subpopulations and NK cells ». Dans 1997 Shanghai International Conference on Laser Medicine and Surgery, sous la direction de Jing Zhu. SPIE, 1998. http://dx.doi.org/10.1117/12.330179.
Texte intégralSantinon, François, Maxime Batignes, Charlotte Pouchy, Benoit Salomon, Patrice Decker, Marie-Christophe Boissier, Luca Semerano et Natacha Bessis. « 03.12 Tnfr2+regulatory t cells subpopulations are highly suppressive and are increased on anti-tnf treatment ». Dans 37th European Workshop for Rheumatology Research 2–4 March 2017 Athens, Greece. BMJ Publishing Group Ltd and European League Against Rheumatism, 2017. http://dx.doi.org/10.1136/annrheumdis-2016-211049.12.
Texte intégralZhu, Jing, et Fan Ni. « The effects of ILLLI on peripheral blood T lymphocytes subpopulation and NK cells in psoriasis treatment ». Dans 2004 Shanghai international Conference on Laser Medicine and Surgery, sous la direction de Jing Zhu. SPIE, 2005. http://dx.doi.org/10.1117/12.639326.
Texte intégralRapports d'organisations sur le sujet "T-cell subpopulations"
Splitter, Gary, Zeev Trainin et Yacov Brenner. Lymphocyte Response to Genetically Engineered Bovine Leukemia Virus Proteins in Persistently Lymphocytic Cattle from Israel and the U.S. United States Department of Agriculture, juillet 1995. http://dx.doi.org/10.32747/1995.7570556.bard.
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