Littérature scientifique sur le sujet « Sclerosi multipla peptides »
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Articles de revues sur le sujet "Sclerosi multipla peptides"
Bourdette, D. N., E. Edmonds, C. Smith, J. D. Bowen, C. RG Guttmann, Z. P. Nagy, J. Simon et al. « A highly immunogenic trivalent T cell receptor peptide vaccine for multiple sclerosis ». Multiple Sclerosis Journal 11, no 5 (octobre 2005) : 552–61. http://dx.doi.org/10.1191/1352458505ms1225oa.
Texte intégralMatsoukas, John, George Deraos, Kostas Kelaidonis, Md Kamal Hossain, Jack Feehan, Andreas G. Tzakos, Elizabeth Matsoukas, Emmanuel Topoglidis et Vasso Apostolopoulos. « Myelin Peptide–Mannan Conjugate Multiple Sclerosis Vaccines : Conjugation Efficacy and Stability of Vaccine Ingredient ». Vaccines 9, no 12 (8 décembre 2021) : 1456. http://dx.doi.org/10.3390/vaccines9121456.
Texte intégralBourdette, D. N., R. H. Whitham, Y. K. Chou, W. J. Morrison, J. Atherton, C. Kenny, D. Liefeld, G. A. Hashim, H. Offner et A. A. Vandenbark. « Immunity to TCR peptides in multiple sclerosis. I. Successful immunization of patients with synthetic V beta 5.2 and V beta 6.1 CDR2 peptides. » Journal of Immunology 152, no 5 (1 mars 1994) : 2510–19. http://dx.doi.org/10.4049/jimmunol.152.5.2510.
Texte intégralPlanas, Raquel, Radleigh Santos, Paula Tomas-Ojer, Carolina Cruciani, Andreas Lutterotti, Wolfgang Faigle, Nicole Schaeren-Wiemers et al. « GDP-l-fucose synthase is a CD4+ T cell–specific autoantigen in DRB3*02:02 patients with multiple sclerosis ». Science Translational Medicine 10, no 462 (10 octobre 2018) : eaat4301. http://dx.doi.org/10.1126/scitranslmed.aat4301.
Texte intégralOwens, Gregory P., Andrew J. Shearer, Xiaoli Yu, Alanna M. Ritchie, Kathryne M. Keays, Jeffrey L. Bennett, Donald H. Gilden et Mark P. Burgoon. « Screening Random Peptide Libraries with Subacute Sclerosing PanencephalitisBrain-Derived Recombinant Antibodies Identifies Multiple Epitopes in the C-Terminal Region of the Measles Virus Nucleocapsid Protein ». Journal of Virology 80, no 24 (15 décembre 2006) : 12121–30. http://dx.doi.org/10.1128/jvi.01704-06.
Texte intégralBeddow, Sara A., Tobias Neef, Igal Ifergan, Joseph R. Podojil, Daniel Getts et Stephen D. Miller. « Treatment with Multiple-linked Myelin Peptides Encapsulated within Nanoparticles Induces Antigen-specific Tolerance in SJL/J Relapsing-remitting Experimental Autoimmune Encephalomyelitis ». Journal of Immunology 204, no 1_Supplement (1 mai 2020) : 160.10. http://dx.doi.org/10.4049/jimmunol.204.supp.160.10.
Texte intégralBronstein, J. M., R. Lallone, R. S. Seitz, G. W. Ellison et L. W. Myers. « A humoral response to OSP in multiple sclerosis : A molecular mimic ? » Multiple Sclerosis Journal 2, no 5 (décembre 1996) : 250. http://dx.doi.org/10.1177/135245859600200512.
Texte intégralMatsoukas, John M., Irene Ligielli, Christos T. Chasapis, Konstantinos Kelaidonis, Vasso Apostolopoulos et Thomas Mavromoustakos. « Novel Approaches in the Immunotherapy of Multiple Sclerosis : Cyclization of Myelin Epitope Peptides and Conjugation with Mannan ». Brain Sciences 11, no 12 (29 novembre 2021) : 1583. http://dx.doi.org/10.3390/brainsci11121583.
Texte intégralAndroutsou, Maria-Eleni, Agathi Nteli, Areti Gkika, Maria Avloniti, Anastasia Dagkonaki, Lesley Probert, Theodore Tselios et Simona Golič Grdadolnik. « Characterization of Asparagine Deamidation in Immunodominant Myelin Oligodendrocyte Glycoprotein Peptide Potential Immunotherapy for the Treatment of Multiple Sclerosis ». International Journal of Molecular Sciences 21, no 20 (13 octobre 2020) : 7566. http://dx.doi.org/10.3390/ijms21207566.
Texte intégralBourdette, Dennis N., Yuan K. Chou, Ruth H. Whitham, Jane Buckner, Hi Jong Kwon, Gerald T. Nepom, Abigail Buenafe et al. « Immunity to T Cell Receptor Peptides in Multiple Sclerosis. III. Preferential Immunogenicity of Complementarity-Determining Region 2 Peptides from Disease-Associated T Cell Receptor BV Genes* ». Journal of Immunology 161, no 2 (15 juillet 1998) : 1034–44. http://dx.doi.org/10.4049/jimmunol.161.2.1034.
Texte intégralThèses sur le sujet "Sclerosi multipla peptides"
Kissler, Stephan. « How transgenic T cells interpret encounter with peptide antigen ». Thesis, University of Bristol, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.324380.
Texte intégralAllen, Stephanie D. « Therapeutic peptidomimetic strategies for costimulation blockade in multiple sclerosis and transplantation / conformational peptide vaccines of the HER-2/neu dimerization loop are effective in inhibiting mammary tumor growth in vivo ». Columbus, Ohio : Ohio State University, 2006. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1150479940.
Texte intégralKanthamneni, Naveen. « Development of Immunosupressant and Peptide Loaded Microparticles as Tolerogenic Vaccines for Treatment of Autoimmune Diseases ». The Ohio State University, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=osu1331050212.
Texte intégralVargas, Sanchez Jeinny. « In vivo peptide biomarker screening for molecular imaging in eae neuroinflammation ». Thesis, Bordeaux 2, 2013. http://www.theses.fr/2013BOR22102/document.
Texte intégralIn neurodegenerative disorders like multiple sclerosis, neuroinflammation modifies the blood brain barrier (BBB) status by causing complex cellular and molecular alterations. Characterization of such molecular changes by an in vivo labeling approach is most challenging to generate reliable in vivo targeting tools and biomarkers. In vivo strategies to define such markers are, however, hampered by the plethora of the accessible target molecules, the vicinity of diseased target expression among healthy tissue and the potentially structural alterations of target molecules when studied by histopathology. The aim of this work is to streamline the biomarker discovery of pathological molecular tissue alterations by in vivo selection of phage displayed peptide repertoires that are further submitted to physical DNA subtraction (“PhiSSH”) of sequences encoding common peptides in both repertoires (HEALTHY and PATHOLOGY). The strategy of Subtraction allows thus the enrichment of clones specific for one repertoire and is of particular interest for complex repertoires produced by in vivo selection. We present the application of this strategy in the multiple sclerosis rat model, Experimental Autoimmune Encephalomyelitis (EAE) pathology, where target lesions are disseminated in the central nervous system (CNS) generating a large amount of clones binding to healthy tissue among the recovered repertoire clones binding to the lesions by comparison with healthy control rats. The efficiency of the subtraction was monitored by massive sequencing of the three repertoires, «EAE», «HEALTHY», and «SUBTRACTION». More than 95% of the clones common to EAE and Healthy repertoires were shown to be absent from the Subtraction repertoire. A set of randomly chosen clones and synthesized peptides from the EAE and subtraction repertoires were tested for differential labeling of a) diseased and healthy animal tissues and b) an in vitro BBB model, in IL-1ß challenged and resting control state culture human cells (hCMEC/D3). One of the phage clones and 4 chemically synthesized peptides showed specific binding to brain ECs in neuro-inflammatory conditions. Using a strategy of crosslinking of an EAE specific phage clone on protein targets expressed by IL-1ß activated ECs followed by mass spectrometry, we propose hypothetically Galectin-1 as a possible target of this phage. PhiSSH will be useful for in vivo screening of small peptide combinatorial libraries for the discovery of biomarkers specific of molecular and cellular alterations untangled with healthy tissues, as in most pathologies presenting neuroinflammatory activity
Schirer, Alicia. « Les maladies neurodégénératives : étude de peptides modèles, de tissus cérébraux et de liquides céphalorachidiens par (micro)spectroscopie infrarouge et Raman ». Thesis, Strasbourg, 2016. http://www.theses.fr/2016STRAF055/document.
Texte intégralNeurodegenerative diseases represent a major societal challenge. So, it is necessary to develop new tools for a better understanding and diagnosing of these diseases. Infrared (IR) and Raman spectroscopies seem to be good candidates since they can characterize the physiopathological conditions of a biological sample. The purpose of this thesis was to apply these methods to the study of model peptides, brain tissues and cerebrospinal fluids (CSF). As a part of brain tissue analysis, IR and Raman spectroscopy were coupled to microscopy in order to combine spectral and spatial information. This methodology improved our understanding of the formation and the role of amyloid plaques in Alzheimer’s disease (AD). Moreover, it allowed to demonstrate the potential of these approaches in future studies on the effect of various treatments against multiple sclerosis. Concerning the study of CSF, IR-ATR and surface enhanced Raman spectroscopy were applied to identify spectroscopic markers of AD and Lewy body disease that could enable early diagnosis of these diseases and discrimination between them
Becquet, Laurine. « Evaluation des effets thérapeutiques de neuropeptides contre la sclérose en plaques : les orexines, le vasoactive intestinal peptide, le pituitary adenylate cyclase-activating polypeptide et leurs analogues ». Thesis, Normandie, 2018. http://www.theses.fr/2018NORMR071.
Texte intégralMultiple sclerosis (MS) is a chronic autoimmune and neurodegenerative disease of the central nervous system (CNS). First MS symptoms are cognitive deterioration, dizziness, pain, fatigue and loss of vision. In physiological condition, the axons of neurons are surrounded by a myelin sheath synthesized by oligodendrocytes to accelerate the conduction velocity of nerve impulses and to prevent neuronal death. The most widely used experimental model of MS is the EAE model. After immunization against MOG35-55, self-reactive Th1 and Th17 cells induce an acute inflammatory response at the periphery and then migrate into the SNC. Then they induce an inflammatory response against myelin, with the intervention of myeloid cells. This results in the destruction of myelin sheaths decreasing the rate of conduction of nerve impulses and axonal loss, responsible for the aforementioned symptoms. Currently, MS treatments can slow the progression of paralysis and decrease the severity and the incidence of symptoms by targeting immune responses. However, these treatments have no effect on the progressive forms of the disease when the neurodegenerative processes amplify and dominate the inflammatory component. It is therefore necessary to find effective therapies that can both block inflammation and also promote remyelination and neuroregeneration.In this context, new therapeutic targets have emerged to treat MS: VIP, PACAP, orexin A, their receptors and their analogs. These neuropeptides have several effects such as anti-inflammatory and neuroprotective activities. My thesis works were focused on the effect of a VPAC2 receptor agonist, one of the three receptors of VIP and PACAP, and orexin A in inflammatory and neurodegenerative processes during MOG35-55-induced EAE model and toxic model using CPZ, which induces mature oligodendrocyte death and demyelination without the influence of lymphocytes.A short term and systemic treatment of BAY55-9837, a VPAC2 agonist, decreases chronic EAE severity with less activation of T lymphocytes and antigen presentation activities of dendritic cells and monocytes as well as Treg population modulation at the periphery. In the CNS, immune cell infiltration is reduced in VPAC2-treated mice compared to PBS-treated mice with an higher microglia/macrophage proportion. Moreover, VPAC2 agonist decreases demyelination processes and enhances remyelination during cuprizone model. In parallel, short term and intraperitoneal administration of orexin A decreases drastically the severity of chronic EAE. Orexin A treatment has no effect on immunization phase of EAE but limits effective phase with a lower infiltration of CD4+ T lymphocytes, inflammatory mediators, demyelination, astrogliosis and microglial activation in the CNS. In contrast, systemic administration of orexin A seems to have no effect during demyelination and remyelination phases in CPZ model
Mazzoleni, Antonio. « Glucosylated peptides in autoimmune diseases : synthetic strategies and application to antibody detection and capture ». Doctoral thesis, 2020. http://hdl.handle.net/2158/1197513.
Texte intégralSibilla, Antonio. « Use of the non-peptidic Nerve Growth Factor mimetic MT2 to activate TrkA and TrkB receptors : a therapeutic tool in Multiple Sclerosis ». Doctoral thesis, 2018. http://hdl.handle.net/2158/1178147.
Texte intégralDargahi, Narges. « Immune modulation using probiotics and multiple sclerosis peptides ». Thesis, 2019. https://vuir.vu.edu.au/41847/.
Texte intégralΔεράος, Σπύρος. « Σχεδιασμός και σύνθεση αναλόγων επιτόπων της μυελίνης καθώς και αναλόγων της Β αλυσίδας του υποδοχέα της ιντερλευκίνης-2 : μελέτη δομής - βιολογικής δραστηριότητας ». Thesis, 2003. http://nemertes.lis.upatras.gr/jspui/handle/10889/3451.
Texte intégralChapitres de livres sur le sujet "Sclerosi multipla peptides"
Ebringer, Alan. « Antibodies to Prion and Acinetobacter Peptide Sequences in Bovine Spongiform Encephalopathy ». Dans Multiple Sclerosis, Mad Cow Disease and Acinetobacter, 79–86. Cham : Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-02735-7_10.
Texte intégralEbringer, Alan. « Antibodies to Acinetobacter Peptide Sequences Resembling Myelin and Neurofilaments in Multiple Sclerosis Patients ». Dans Multiple Sclerosis, Mad Cow Disease and Acinetobacter, 97–107. Cham : Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-02735-7_12.
Texte intégralEbringer, Alan. « Antibodies to Short Synthetic Acinetobacter and Pseudomonas Peptide Sequences Resembling Myelin and Neurofilaments in Multiple Sclerosis Patients ». Dans Multiple Sclerosis, Mad Cow Disease and Acinetobacter, 119–29. Cham : Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-02735-7_14.
Texte intégralKurnellas, Michael P., Jonathan B. Rothbard et Lawrence Steinman. « Self-Assembling Peptides Form Immune Suppressive Amyloid Fibrils Effective in Autoimmune Encephalomyelitis ». Dans Emerging and Evolving Topics in Multiple Sclerosis Pathogenesis and Treatments, 221–32. Cham : Springer International Publishing, 2015. http://dx.doi.org/10.1007/7854_2015_377.
Texte intégralCarotenuto, Alfonso, Armida Di Fenza, Elena Nardi, Anna M. Papini et Paolo Rovero. « Conformational Studies of a Glycopeptide Recognized with High Affinity by Autoantibodies in Multiple Sclerosis ». Dans Peptides : The Wave of the Future, 340–41. Dordrecht : Springer Netherlands, 2001. http://dx.doi.org/10.1007/978-94-010-0464-0_156.
Texte intégralBrocke, S. « T Cell Receptor Peptides for the Vaccination Therapy of Multiple Sclerosis ». Dans Therapeutic Vaccination Strategies, 167–79. Berlin, Heidelberg : Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-662-04183-3_11.
Texte intégralBlalock, J. Edwin. « Neuroendocrine Peptide Hormones and their Receptors as Endogenous Components of the Immune System ». Dans Cellular and Humoral Immunological Components of Cerebrospinal Fluid in Multiple Sclerosis, 443–51. Boston, MA : Springer US, 1987. http://dx.doi.org/10.1007/978-1-4899-5348-3_51.
Texte intégralArnon, Ruth, Michael Sela et Rina Aharoni. « Peptides and Polypeptides as Immunomodulators and Their Consequential Therapeutic Effect in Multiple Sclerosis and Other Autoimmune Diseases ». Dans Peptide Drug Discovery and Development, 313–35. Weinheim, Germany : Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527636730.ch15.
Texte intégralBielekova, B., et R. Martin. « Specific Immunotherapy of Multiple Sclerosis by Altered Peptide Ligands — Risk or Benefit ? » Dans New Concepts in Pathology and Treatment of Autoimmune Disorders, 69–87. Berlin, Heidelberg : Springer Berlin Heidelberg, 2001. http://dx.doi.org/10.1007/978-3-662-04450-6_5.
Texte intégralTzoupis, Haralambos, et Theodore Tselios. « In Silico Drug Design : Non-peptide Mimetics for the Immunotherapy of Multiple Sclerosis ». Dans Methods in Molecular Biology, 33–47. New York, NY : Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-8630-9_3.
Texte intégralActes de conférences sur le sujet "Sclerosi multipla peptides"
Vezenkov, Lyubomir, Borislav Anchev, Ivanka Kostadinova, Kristian Fidanov, Daniela S. Tsekova, Nikolay G. Vasilev et Nikolai D. Danchev. « New 4-Aminopyridine derivatives containing peptide fragment designed for the treatment of Alzheimer disease and multiple sclerosis ». Dans 35th European Peptide Symposium. Prompt Scientific Publishing, 2018. http://dx.doi.org/10.17952/35eps.2018.241.
Texte intégralCasoria, Michele, Paolo Rovero, Gianni Cardini, Marina Macchiagodena, Anna Maria Papini, Claudia Andreini et Marco Pagliai. « From a Bioinformatic Approach to Synthetic Conformational Peptide Epitopes to Disclose Molecular Mechanism of Aberrant Glucosylation in Multiple Sclerosis ». Dans 36th European Peptide Symposium. The European Peptide Society, 2022. http://dx.doi.org/10.17952/36eps/36eps.2022.237.
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