调节性T细胞在乳腺癌中的多重作用。

IF 4.7 2区 医学 Q1 ONCOLOGY
Kevin Kos, Karin E de Visser
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引用次数: 19

摘要

乳腺癌的微环境承载着免疫系统不同参与者之间的动态串扰。虽然细胞毒性免疫细胞能够控制肿瘤的生长和转移,但肿瘤破坏的免疫抑制免疫细胞会努力损害有效免疫并促进肿瘤的进展。其中,调节T细胞(Tregs),免疫稳态的守门人,在乳腺癌中扮演着多方面的角色。有趣的是,临床观察表明,血液和肿瘤内Tregs可能具有很强的预后价值,这取决于乳腺癌亚型。因此,新出现的临床前证据表明Tregs在乳腺癌的发生和发展中起着核心作用,并为转移形成提供关键支持。在这里,Tregs不仅对免疫逃逸很重要,而且还独立于其免疫调节能力促进肿瘤进展。将Treg生物学的见解与快速发展的免疫肿瘤学领域的进展相结合,有望为设计更有效的免疫治疗策略奠定基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The Multifaceted Role of Regulatory T Cells in Breast Cancer.

The Multifaceted Role of Regulatory T Cells in Breast Cancer.

The microenvironment of breast cancer hosts a dynamic cross talk between diverse players of the immune system. While cytotoxic immune cells are equipped to control tumor growth and metastasis, tumor-corrupted immunosuppressive immune cells strive to impair effective immunity and promote tumor progression. Of these, regulatory T cells (Tregs), the gatekeepers of immune homeostasis, emerge as multifaceted players involved in breast cancer. Intriguingly, clinical observations suggest that blood and intratumoral Tregs can have strong prognostic value, dictated by breast cancer subtype. Accordingly, emerging preclinical evidence shows that Tregs occupy a central role in breast cancer initiation and progression and provide critical support to metastasis formation. Here, Tregs are not only important for immune escape but also promote tumor progression independent of their immune regulatory capacity. Combining insights into Treg biology with advances made across the rapidly growing field of immuno-oncology is expected to set the stage for the design of more effective immunotherapy strategies.

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来源期刊
CiteScore
14.50
自引率
1.30%
发文量
13
期刊介绍: The Annual Review of Cancer Biology offers comprehensive reviews on various topics within cancer research, covering pivotal and emerging areas in the field. As our understanding of cancer's fundamental mechanisms deepens and more findings transition into targeted clinical treatments, the journal is structured around three main themes: Cancer Cell Biology, Tumorigenesis and Cancer Progression, and Translational Cancer Science. The current volume of this journal has transitioned from gated to open access through Annual Reviews' Subscribe to Open program, ensuring all articles are published under a CC BY license.
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