首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Circulating tumor antigen-specific regulatory T cells in patients with metastatic melanoma
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Circulating tumor antigen-specific regulatory T cells in patients with metastatic melanoma

机译:转移性黑色素瘤患者的循环肿瘤抗原特异性调节性T细胞

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摘要

Although it is accepted that regulatory T cells (T regs) contribute to cancer progression, most studies in the field consider nonantigen-specif ic 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.
机译:尽管公认调节性T细胞(T regs)有助于癌症进展,但该领域的大多数研究都考虑了非抗原特异性抑制。在这里,我们显示了转移性黑素瘤患者血液中存在肿瘤抗原特异性CD4〜+ T regs。这些CD4 + T regs识别广泛的肿瘤抗原,包括gp100和TRP1(黑色素瘤组织分化抗原),NY-ESO-1(癌症/睾丸抗原)和survivin(凋亡蛋白(IAP)家族抗原抑制剂)。这些肿瘤抗原特异性T regs响应特定的15-mer肽在外周血单核细胞(PBMC)培养物中增殖,优先产生IL-10并表达高水平的FoxP3。它们以细胞接触依赖性的方式抑制自体CD4〜+ CD25 T细胞应答,因此共享天然存在的调节性T细胞和1型调节性T细胞的特性。在健康个体中未检测到此类肿瘤抗原特异性T reg。这些肿瘤抗原特异性T regs因此可能代表转移性黑色素瘤免疫治疗的另一个目标。

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