Targeting antigen presentation in autoimmunity

被引:9
|
作者
Lees, Jason R. [1 ]
机构
[1] Uniformed Serv Univ Hlth Sci, Dept Med, Room A3060, Bethesda, MD 20814 USA
关键词
Antigen presentation; Autoimmunity; Inflammation; Immune regulation; CD8(+) T-CELLS; NONOBESE DIABETIC MICE; CENTRAL-NERVOUS-SYSTEM; DENDRITIC CELLS; IN-VIVO; B-CELLS; ANTIBODY PREVENTS; ANIMAL-MODEL; GENETIC RISK; LYMPH-NODES;
D O I
10.1016/j.cellimm.2018.12.006
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Autoimmune diseases are heterogeneous group of disorders that together represent an enormous societal and medical problem. CD4+ T cells have critical roles in the initiation and pathogenesis of autoimmune disease. As such, modulation of T cell activity has proven to have significant therapeutic effects in multiple autoimmune settings. T cell activation is a complex process with multiple potential therapeutic targets, many of which have been successfully utilized to treat human disease. Current pharmacological treatment largely targets T cell intrinsic activities as a means of treating various autoimmune disorders. Here I review extant and potential therapeutic approaches that instead specifically target antigen presentation to CD4+ T cells as a critical checkpoint in autoimmune responses. In addition, the contribution of antigen modulation components in current therapeutic approaches is considered along with the impact of new antigen targeted treatment modalities. Finally, potential challenges are considered in the context of the potential for antigen specific targeting of the antigen presentation process.
引用
收藏
页码:4 / 9
页数:6
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