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Intrinsic Mechanisms Regulating T Cell Tolerance in Autoimmune Diabetes

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서명/저자사항Intrinsic Mechanisms Regulating T Cell Tolerance in Autoimmune Diabetes.
개인저자Zhang, Qianxia.
단체저자명University of Pittsburgh.
발행사항[S.l.]: University of Pittsburgh., 2018.
발행사항Ann Arbor: ProQuest Dissertations & Theses, 2018.
형태사항171 p.
기본자료 저록Dissertation Abstracts International 80-01B(E).
Dissertation Abstract International
ISBN9780438364943
학위논문주기Thesis (Ph.D.)--University of Pittsburgh, 2018.
일반주기 Source: Dissertation Abstracts International, Volume: 80-01(E), Section: B.
Adviser: Dario A. A. Vignali.
요약Type 1 Diabetes (T1D) is a polygenic autoimmune disease characterized by immune cell infiltration into the islets of Langerhans, destruction of insulin-producing beta cells, and uncontrolled hyperglycemia. Islet-antigen reactive CD4+ and CD8+ T
요약Lymphocyte Activation Gene 3 (LAG3, CD223), a co-inhibitory receptor highly expressed on T cells, is one of these essential mechanisms that intrinsically regulate T cell tolerance in autoimmune diabetes. I evaluate the role of LAG3 on T cells ve
요약In addition to dissecting the role of LAG3 in regulating T cell tolerance, I also show that removal of programmed death protein 1 (PD1) or overexpression of Neuropilin 1 (Nrp1) on Tregs protect NOD mice from autoimmune diabetes in Appendix A and
일반주제명Immunology.
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