T-cell stimulation and regulation: With complements from CD46

被引:44
作者
Kemper, C
Verbsky, JW
Price, JD
Atkinson, JP
机构
[1] Washington Univ, Sch Med, Div Rheumatol, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Dept Pediat, St Louis, MO 63110 USA
[4] Washington Univ, Sch Med, Grad Program Immunol, St Louis, MO 63110 USA
关键词
CD46; complement; T-regulatory T-cells; immunosuppression; interleukin-10;
D O I
10.1385/IR:32:1-3:031
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Crosslinking of CD46 and CD3 on naive human CD41 T-lymphocytes induces interleukin- 10 secretion and granzyme B expression. These highly proliferative T-regulatory type I-like T-regulatory T-cells (Tregs) can suppress an immune response. We propose that this process is important in the prevention of chronic inflammation such as at epithelial borders and in deactivation of a successful immune response. Relative to the latter, once a complement-fixing polyclonal antibody response has been mounted, in most cases, the pathogen will be rapidly destroyed. At this time, the C3b/C4b-bearing immune complexes could initiate the deactivation arm of an immune response by shutting down immunocompetent cells through CD46-generated T-cells. Herein, we review this pathway for the induction of Tregs, focusing on a role for the complement system and especially signaling through CD46 on human T-cells.
引用
收藏
页码:31 / 43
页数:13
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