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CD4+ CD25+ 调节性T细胞控制癌症患者抗原特异性CD4+ 辅助性T细胞反应的诱导。

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

作者信息

Nishikawa Hiroyoshi, Jäger Elke, Ritter Gerd, Old Lloyd J, Gnjatic Sacha

机构信息

Ludwig Institute for Cancer Research, New York Branch at Memorial Sloan-Kettering Cancer Center, 1275 York Ave, Box 32/Rm K-817, New York, NY 10021, USA.

出版信息

Blood. 2005 Aug 1;106(3):1008-11. doi: 10.1182/blood-2005-02-0607. Epub 2005 Apr 19.

Abstract

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.

摘要

一部分癌症患者会自然产生针对NY-ESO-1的CD4+辅助性T细胞1型(Th1)细胞应答,这种应答与抗NY-ESO-1血清抗体相关。为了探讨T细胞调节在自发性肿瘤免疫控制中的作用,我们在体外分析了CD4+CD25+ T细胞耗竭之前或之后NY-ESO-1特异性Th1细胞的诱导情况。在NY-ESO-1血清阳性的癌症患者中,Th1细胞在CD25+ T细胞存在的情况下产生,而血清阴性的癌症患者和健康供体则需要耗竭CD25+ T细胞才能在体外诱导出NY-ESO-1特异性Th1细胞。在体外,新产生的NY-ESO-1特异性Th1细胞来源于初始前体细胞,而仅在有NY-ESO-1抗体的患者中可检测到预先存在的记忆细胞群。记忆细胞群比初始细胞群对CD4+CD25+调节性T细胞的敏感性更低。我们认为CD4+CD25+调节性T细胞参与了NY-ESO-1特异性抗肿瘤免疫的产生和调节。

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