Antigen-specific T cell responses in autoimmune diabetes

被引:1
|
作者
Dwyer, Alexander J. [1 ]
Shaheen, Zachary R. [2 ]
Fife, Brian T. [1 ]
机构
[1] Univ Minnesota, Med Sch, Ctr Immunol, Dept Med,Div Rheumat & Autoimmune Dis, Minneapolis, MN USA
[2] Univ Minnesota, Med Sch, Ctr Immunol, Dept Pediat Pediat Rheumatol Allergy & Immunol, Minneapolis, MN 55455 USA
来源
FRONTIERS IN IMMUNOLOGY | 2024年 / 15卷
基金
美国国家卫生研究院;
关键词
autoimmune diabetes; autoantigens; T cells; hybrid insulin peptides; antigen specific therapy; PANCREATIC BETA-CELLS; MHC CLASS-II; GLUTAMIC-ACID DECARBOXYLASE; NECROSIS-FACTOR-ALPHA; NOD MOUSE MODEL; DENDRITIC CELLS; NITRIC-OXIDE; CHROMOGRANIN-A; RECENT-ONSET; INSULIN-SECRETION;
D O I
10.3389/fimmu.2024.1440045
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Autoimmune diabetes is a disease characterized by the selective destruction of insulin-secreting beta-cells of the endocrine pancreas by islet-reactive T cells. Autoimmune disease requires a complex interplay between host genetic factors and environmental triggers that promote the activation of such antigen-specific T lymphocyte responses. Given the critical involvement of self-reactive T lymphocyte in diabetes pathogenesis, understanding how these T lymphocyte populations contribute to disease is essential to develop targeted therapeutics. To this end, several key antigenic T lymphocyte epitopes have been identified and studied to understand their contributions to disease with the aim of developing effective treatment approaches for translation to the clinical setting. In this review, we discuss the role of pathogenic islet-specific T lymphocyte responses in autoimmune diabetes, the mechanisms and cell types governing autoantigen presentation, and therapeutic strategies targeting such T lymphocyte responses for the amelioration of disease.
引用
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页数:22
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