肿瘤微环境中的调节性T细胞:治疗方法和临床意义。

IF 3.3 3区 生物学 Q3 CELL BIOLOGY
Niti Sureka, Sufian Zaheer
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引用次数: 0

摘要

调节性T细胞(Tregs),以前被称为抑制性T细胞,是CD4+ T细胞的一个独特的亚群,专门用于免疫抑制。它们的特征是细胞核内转录因子FoxP3的组成表达,以及细胞表面的CD25 (IL-2受体α-链)和CTLA-4的组成表达。Tregs不仅可以抑制自然杀伤细胞介导的细胞毒性,还可以抑制CD4+和CD8+ t细胞的增殖,抑制免疫细胞分泌干扰素γ,最终损害有效的抗肿瘤免疫应答。Treg细胞被广泛认为是临床肿瘤免疫治疗有效性的重要障碍。大量研究一致表明Treg细胞在促进肿瘤的发生和发展中起着关键作用。相反,Treg细胞的消耗与肿瘤生长和发展的显著延迟有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Regulatory T Cells in Tumor Microenvironment: Therapeutic Approaches and Clinical Implications.

Regulatory T cells (Tregs), previously referred to as suppressor T cells, represent a distinct subset of CD4+ T cells that are uniquely specialized for immune suppression. They are characterized by the constitutive expression of the transcription factor FoxP3 in their nuclei, along with CD25 (the IL-2 receptor α-chain) and CTLA-4 on their cell surface. Tregs not only restrict natural killer cell-mediated cytotoxicity but also inhibit the proliferation of CD4+ and CD8+ T-cells and suppress interferon-γ secretion by immune cells, ultimately impairing an effective antitumor immune response. Treg cells are widely recognized as a significant barrier to the effectiveness of tumor immunotherapy in clinical settings. Extensive research has consistently shown that Treg cells play a pivotal role in facilitating tumor initiation and progression. Conversely, the depletion of Treg cells has been linked to a marked delay in tumor growth and development.

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来源期刊
Cell Biology International
Cell Biology International 生物-细胞生物学
CiteScore
7.60
自引率
0.00%
发文量
208
审稿时长
1 months
期刊介绍: Each month, the journal publishes easy-to-assimilate, up-to-the minute reports of experimental findings by researchers using a wide range of the latest techniques. Promoting the aims of cell biologists worldwide, papers reporting on structure and function - especially where they relate to the physiology of the whole cell - are strongly encouraged. Molecular biology is welcome, as long as articles report findings that are seen in the wider context of cell biology. In covering all areas of the cell, the journal is both appealing and accessible to a broad audience. Authors whose papers do not appeal to cell biologists in general because their topic is too specialized (e.g. infectious microbes, protozoology) are recommended to send them to more relevant journals. Papers reporting whole animal studies or work more suited to a medical journal, e.g. histopathological studies or clinical immunology, are unlikely to be accepted, unless they are fully focused on some important cellular aspect. These last remarks extend particularly to papers on cancer. Unless firmly based on some deeper cellular or molecular biological principle, papers that are highly specialized in this field, with limited appeal to cell biologists at large, should be directed towards journals devoted to cancer, there being very many from which to choose.
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