CD4+ CD25+ regulatory T cells control the induction of antigen-specific CD4+ helper T cell responses in cancer patients

被引:141
作者
Nishikawa, H
Jäger, E
Ritter, G
Old, LJ
Gnjatic, S
机构
[1] Mem Sloan Kettering Canc Ctr, Ludwig Inst Canc Res, New York Branch, New York, NY 10021 USA
[2] Krankenhaus NW Frankfurt, Med Klin 2, Frankfurt, Germany
关键词
D O I
10.1182/blood-2005-02-0607
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A proportion of cancer patients naturally develop CD4(+) T-helper type 1 (Th1) cell responses to NY-ESO-1 that correlate with anti-NY-ESO-1 serum antibodies. To address the role of T-cell regulation in the control of spontaneous tumor immunity, we analyzed NY-ESO-1-specific Th1 cell induction before or after depletion of CD4(+)CD25(+) T cells in vitro. While Th1 cells were generated in the presence of CD25(+) T cells in cancer patients seropositive for NY-ESO-1, seronegative cancer patients and healthy donors required CD25(+) T-cell depletion for in vitro induction of NY-ESO-1-specific Th1 cells. In vitro, newly generated NY-ESO-1-specific Th1 cells were derived from naive precursors, whereas preexisting memory populations were detectable exclusively in patients with NY-ESO-1 antibody. Memory populations were less sensitive than naive populations to CD4(+)CD25(+) regulatory T cells. We propose that CD4(+)CD25(+) regulatory T cells are involved in the generation and regulation of NY-ESO-1-specific antitumor immunity.
引用
收藏
页码:1008 / 1011
页数:4
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