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癌症中的CD25 + CD4 +调节性T细胞。

CD25+ CD4+ regulatory T-cells in cancer.

作者信息

Linehan David C, Goedegebuure Peter S

机构信息

Department of Surgery and Alvin J. Siteman Cancer Center, Washington University School of Medicine, St. Louis, MO 63110, USA.

出版信息

Immunol Res. 2005;32(1-3):155-68. doi: 10.1385/IR:32:1-3:155.

Abstract

Regulatory T-cells (Treg) protect the host from autoimmune disease by suppressing self-reactive immune cells. As such, Treg may also block antitumor immune responses. Recent observations by us and others showed that the prevalence of Treg is increased in cancer patients, particularly in the tumor environment. Our studies in a mouse pancreas cancer model suggest that the tumor actively promotes the accrual of Treg through several mechanisms involving activation of naturally occurring Treg as well as conversion of non-Treg into Treg. Our studies focus on further defining these mechanisms with the ultimate goal of designing strategies that block Treg-mediated suppression in cancer patients.

摘要

调节性T细胞(Treg)通过抑制自身反应性免疫细胞来保护宿主免受自身免疫性疾病的侵害。因此,Treg也可能阻断抗肿瘤免疫反应。我们和其他人最近的观察结果表明,癌症患者中Treg的比例增加,特别是在肿瘤环境中。我们在小鼠胰腺癌模型中的研究表明,肿瘤通过多种机制积极促进Treg的积累,这些机制包括天然存在的Treg的激活以及非Treg向Treg的转化。我们的研究重点是进一步明确这些机制,最终目标是设计出能够阻断癌症患者中Treg介导的免疫抑制的策略。

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