CD25+CD4+T cells contribute to the control of memory CD8+T cells

被引:194
作者
Murakami, M
Sakamoto, A
Bender, J
Kappler, J
Marrack, P
机构
[1] Natl Jewish Med & Res Ctr, Howard Hughes Med Inst, Denver, CO 80206 USA
[2] Natl Jewish Med & Res Ctr, Intergrated Dept Immunol, Denver, CO 80206 USA
[3] Univ Colorado, Hlth Sci Ctr, Denver, CO 80206 USA
[4] Univ Colorado, Hlth Sci Ctr, Dept Biochem & Mol Biol, Denver, CO 80206 USA
[5] Univ Colorado, Hlth Sci Ctr, Dept Pharmacol & Med, Denver, CO 80206 USA
关键词
D O I
10.1073/pnas.132254399
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Previously we demonstrated that IL-15 and IL-2 control the number of memory CD8+ T cells in mice. IL-15 induces, and IL-2 suppresses the division of these cells. Here we show that CD25+CD4+ regulatory T cells play an important role in the IL-2-mediated control of memory phenotype CD8+ T cell number. in animals, the numbers of CD25+CD4+ T cells were inversely correlated with the numbers of memory phenotype CD8+ T cells with age. Treatment with anti-IL-2 caused CD25+CD4+ T cells to disappear and, concurrently, increased the numbers of memory phenotype CD8+ T cells. This increase in the numbers of CD8+ memory phenotype T cells was not manifest in animals lacking CD4+ cells. Importantly, adoptive transfer of CD25+CD4+ T cells significantly reduced division of memory phenotype CD8+ T cells. Thus, we conclude that CD25+CD4+ T cells are involved in the IL-2-mediated inhibition of memory CD8+ T cell division and that IL-2 controls memory phenotype CD8+ T cell numbers at least in part through maintenance of the CD25+CD4+ T cell population.
引用
收藏
页码:8832 / 8837
页数:6
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