期刊
JOURNAL OF IMMUNOLOGY
卷 171, 期 7, 页码 3348-3352出版社
AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.171.7.3348
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资金
- NIAID NIH HHS [F32 AI10360, AI466430] Funding Source: Medline
CD28/B7 blockade leads to exacerbated autoimmune disease in the nonobese diabetic mouse strain as a result of a marked reduction in the number of CD4(+) CD25(+) regulatory T cells (Tregs). Herein, we demonstrate that CD28 controls both thymic development and peripheral homeostasis of Tregs. CD28 maintains a stable pool of peripheral Tregs by both supporting their survival and promoting their self-renewal. CD28 engagement promotes survival by regulating IL-2 production by conventional T cells and CD25 expression on Tregs.
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