Regulatory T cells suppress CD8+ T cell responses induced by direct priming and cross-priming and moderate immunodominance disparities

被引:108
作者
Haeryfar, SMM
DiPaolo, RJ
Tscharke, DC
Bennink, JR
Yewdell, JW
机构
[1] NIAID, Viral Dis Lab, NIH, Bethesda, MD 20892 USA
[2] NIAID, Immunol Lab, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.4049/jimmunol.174.6.3344
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Little is known regarding the participation of CD4(+)CD25(+) regulatory T cells (T-reg) in T-CD8(+) responses. In this study, we show that T-reg depletion via treatment with anti-CD25 mAb (PC61) significantly enhances T-CD8(+) responses to influenza A virus, vaccinia virus, and SV40-transformed cells induced by either direct priming or cross-priming. PC61 did not enhance T-CD8(+) responses in CD4-deficient mice, providing the initial demonstration that PC61 acts on a subset of T-CD4(+), and not on other cells that express either CD25 or a fortuitously cross-reactive Ag. We further show that T-reg selectively suppress responses to the most immunodominant T-CD8(+) determinants in the three systems examined. Therefore, T-reg influence T-CD8 immunodominance hierarchies by moderating disparities in responses to different determinants.
引用
收藏
页码:3344 / 3351
页数:8
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