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dc.contributor.authorFLAVELL, RA
dc.contributor.authorTuzun, Erdem
dc.contributor.authorDONG, C
dc.contributor.authorCHRISTADOSS, P
dc.contributor.authorSCOTT, BG
dc.contributor.authorYANG, HA
dc.date.accessioned2021-03-03T08:26:38Z
dc.date.available2021-03-03T08:26:38Z
dc.identifier.citationSCOTT B., YANG H., Tuzun E., DONG C., FLAVELL R., CHRISTADOSS P., "ICOS is essential for the development of experimental autoimmune myasthenia gravis", JOURNAL OF NEUROIMMUNOLOGY, cilt.153, ss.16-25, 2004
dc.identifier.issn0165-5728
dc.identifier.othervv_1032021
dc.identifier.otherav_178577a6-6195-4466-80b0-edf7f7c068ea
dc.identifier.urihttp://hdl.handle.net/20.500.12627/21171
dc.identifier.urihttps://doi.org/10.1016/j.jneuroim.2004.04.019
dc.description.abstractLymphocyte costimulation via the inducible costimulatory molecule (ICOS) is required for effective humoral immunity development. Following immunization with Torpedo acetylcholine receptor (AChR), ICOS gene knockout (KO) mice were highly resistant to clinical experimental autoimmune myasthenia gravis (EAMG) development, had less serum AChR-specific immunoglobulins (Igs), and exhibited a diminutive germinal center (GC) reaction in secondary lymphoid tissues. Lymphocyte proliferation and both Th1 and Th2 differentiation in response to AChR and the AChR dominant alpha146-162 peptide were inhibited by the ICOS gene deficiency. ICOS-mediated lymphocyte costimulation is thus vital to the induction of T cell-mediated humoral immunity to AChR and the development of clinical EAMG. (C) 2004 Elsevier B.V. All rights reserved.
dc.language.isoeng
dc.subjectTemel Bilimler
dc.subjectYaşam Bilimleri
dc.subjectSinirbilim ve Davranış
dc.subjectNEUROSCIENCES
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectİmmünoloji
dc.titleICOS is essential for the development of experimental autoimmune myasthenia gravis
dc.typeMakale
dc.relation.journalJOURNAL OF NEUROIMMUNOLOGY
dc.contributor.department, ,
dc.identifier.volume153
dc.identifier.startpage16
dc.identifier.endpage25
dc.contributor.firstauthorID1937


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