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[调节性T细胞在抗肿瘤免疫反应调节中的作用]

[The role of regulatory T cells in the modulation of anti-tumor immune response].

作者信息

Radosavljević Gordana D, Jovanović Ivan P, Kanjevac Tatjana V, Arsenijević Nebojsa N

出版信息

Srp Arh Celok Lek. 2013 Mar-Apr;141(3-4):262-7. doi: 10.2298/sarh1304262r.

Abstract

Regulatory T cells (Treg) represent a subset of CD4+T cells whose function is to suppress immune responses. Treg lymphocytes can be divided into two subsets: natural nTreg lymphocytes that are developed in the thymus and inducible iTreg lymphocytes, which originate from conventional T lymphocytes on the periphery.The majority of Treg lymphocytes express high levels of interleukin-2 (IL-2) receptor a chain (CD25) and transcription factor FoxP3 (critical for the development and suppressor activity of iTreg lymphocytes). Cancer cells can modulate anti-tumor immune response indirectly, through the activation of Treg lymphocytes. It has been shown that the loss of regulatory function by depletion of tumor-induced Treg lymphocytes may enhance effectors response, resulting in tumor rejection, while the increased number of Treg lymphocytes effectively prevents tumor destruction. nTreg lymphocytes express increasingly CTLA-4 and membrane-bound TGF-beta, which inhibits cytokine production and responses of effectors lymphocytes.iTreg lymphocytes secrete immunosuppressive cytokines such as ILreg-10 and TGF-beta.Treg lymphocytes represent one of important obstruction in anti-tumor immunity.

摘要

调节性T细胞(Treg)是CD4 + T细胞的一个亚群,其功能是抑制免疫反应。Treg淋巴细胞可分为两个亚群:在胸腺中发育的天然nTreg淋巴细胞和源自外周常规T淋巴细胞的诱导性iTreg淋巴细胞。大多数Treg淋巴细胞表达高水平的白细胞介素-2(IL-2)受体α链(CD25)和转录因子FoxP3(对iTreg淋巴细胞的发育和抑制活性至关重要)。癌细胞可通过激活Treg淋巴细胞间接调节抗肿瘤免疫反应。研究表明,通过消耗肿瘤诱导的Treg淋巴细胞来丧失调节功能可能会增强效应细胞反应,导致肿瘤排斥,而Treg淋巴细胞数量的增加则有效地阻止了肿瘤破坏。nTreg淋巴细胞越来越多地表达CTLA-4和膜结合型转化生长因子-β,这会抑制细胞因子的产生和效应淋巴细胞的反应。iTreg淋巴细胞分泌免疫抑制细胞因子,如ILreg-10和转化生长因子-β。Treg淋巴细胞是抗肿瘤免疫中的重要障碍之一。

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