Circulating tumor antigen-specific regulatory T cells in patients with metastatic melanoma

被引:137
作者
Vence, Luis [1 ]
Palucka, A. Karolina [1 ]
Fay, Joseph W. [1 ]
Ito, Tomoki [2 ]
Liu, Yong-Jun [2 ]
Banchereau, Jacques [1 ]
Ueno, Hideki [1 ]
机构
[1] Baylor Univ, Baylor Immunol Res Inst, Dallas, TX 75204 USA
[2] Univ Texas Houston, MD Anderson Canc Ctr, Houston, TX 77030 USA
关键词
foxp3; IL-10; NY-ESO-1;
D O I
10.1073/pnas.0710557105
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
Although it is accepted that regulatory T cells (T regs) contribute to cancer progression, most studies in the field consider nonantigen-specific suppression. Here, we show the presence of tumor antigen-specific CD4(+) T regs in the blood of patients with metastatic melanoma. These CD4+ T regs recognize a broad range of tumor antigens, including gp100 and TRP1 (melanoma tissue differentiation antigens), NY-ESO-1 (cancer/testis antigen) and survivin (inhibitor of apoptosis protein (IAP) family antigen). These tumor antigen-specific T regs proliferate in peripheral blood mononuclear cells (PBMC) cultures in response to specific 15-mer peptides, produce preferentially IL-10 and express high levels of FoxP3. They suppress autologous CD4(+)CD25(-) T cell responses in a cell contact-dependent manner and thus share properties of both naturally occurring regulatory T cells and type 1 regulatory T cells. Such tumor antigen-specific T regs were not detected in healthy individuals. These tumor antigen-specific T regs might thus represent another target for immunotherapy of metastatic melanoma.
引用
收藏
页码:20884 / 20889
页数:6
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