The Initial Phase of an Immune Response Functions to Activate Regulatory T Cells

被引:112
|
作者
O'Gorman, William E. [2 ]
Dooms, Hans [1 ]
Thorne, Steve H. [3 ,4 ]
Kuswanto, Wilson F. [1 ]
Simonds, Erin F. [2 ]
Krutzik, Peter O. [2 ]
Nolan, Garry P. [2 ]
Abbas, Abul K. [1 ]
机构
[1] Univ Calif San Francisco, Sch Med, Dept Pathol, San Francisco, CA 94143 USA
[2] Stanford Univ, Sch Med, Dept Microbiol & Immunol, Baxter Lab Genet Pharmacol, Stanford, CA 94305 USA
[3] Univ Pittsburgh, Div Surg Oncol, Pittsburgh, PA 15213 USA
[4] Univ Pittsburgh, Dept Immunol, Pittsburgh, PA 15213 USA
来源
JOURNAL OF IMMUNOLOGY | 2009年 / 183卷 / 01期
基金
美国国家卫生研究院;
关键词
PHOSPHOSPECIFIC FLOW-CYTOMETRY; IN-VIVO; INTERLEUKIN-2; SUPPRESSION; PROTEIN; MEMORY; SELF; PROLIFERATION; INDUCTION; INFECTION;
D O I
10.4049/jimmunol.0900691
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
An early reaction of CD4(+) T lymphocytes to Ag is the production of cytokines, notably IL-2. To detect cytokine-dependent responses, naive Ag-specific T cells were stimulated in vivo and the presence of phosphorylated STAT5 molecules was used to identify the cell populations responding to IL-2. Within hours of T cell priming, IL-2-dependent STAT5 phosphorylation occurred primarily in Foxp3(+) regulatory T cells. In contrast, the Ag-specific T cells received STAT5 signals only after repeated Ag exposure or memory differentiation. Regulatory T cells receiving IL-2 signals proliferated and developed enhanced suppressive activity. These results indicate that one of the earliest events in a T cell response is the activation of endogenous regulatory cells, potentially to prevent autoimmunity. The Journal of Immunology, 2009, 183: 332-339.
引用
收藏
页码:332 / 339
页数:8
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