Cutting edge: CD28 controls dominant regulatory T cell activity during active immunization

被引:14
作者
Lyddane, Clay
Gajewska, Beata U.
Santos, Elmer
King, Philip D.
Furtado, Glaucia C.
Sadelain, Michel [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Gene Transfer & Somat Cell Engn Lab, New York, NY 10021 USA
[2] Mem Sloan Kettering Canc Ctr, Program Immunol, New York, NY 10021 USA
[3] Mem Sloan Kettering Canc Ctr, Dept Radiol, New York, NY 10021 USA
[4] Univ Michigan, Program Immunol, Ann Arbor, MI 48109 USA
[5] CUNY Mt Sinai Sch Med, Immunobiol Ctr, New York, NY 10029 USA
关键词
D O I
10.4049/jimmunol.176.6.3306
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Ligation of CD28 during Ag recognition plays an important role in the generation of effective T cell responses. However, its peripheral control of regulatory T cell function remains obscure. In this study, we show that naive wild-type or CD28(-/-) CD4(+) CD25(-) T cells exposed to peptide in vivo develop regulatory activity that suppresses the response of adoptively transferred naive T cells to a subsequent immunogenic challenge. We find that although CD28 is engaged during the initial peptide-priming event and is essential to sustain T cell survival, it is not sufficient to prevent the dominance of regulatory T cell function. Immunization with adjuvant abrogates regulatory dominance, reducing overall Toxp3 expression in a CD28-dependent manner. We conclude that CD28 licenses active immunization by regulating Ag-induced immunoregulation.
引用
收藏
页码:3306 / 3310
页数:5
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