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肿瘤微环境中调节性 B 细胞的诱导机制及其对免疫抑制和促肿瘤反应的贡献。

Mechanisms of induction of regulatory B cells in the tumour microenvironment and their contribution to immunosuppression and pro-tumour responses.

机构信息

Centre for Oral Immunobiology and Regenerative Medicine, Barts & The London School of Medicine and Dentistry, Queen Mary University of London, Blizard Institute, 4 Newark Street, London E1 2AT, UK.

Division of Infection & Immunity, Faculty of Medical Sciences, Department of Infection, Immunity, and Transplantation, University College London. The Pears Building, Rowland Hill St, London NW3 2PP, UK.

出版信息

Clin Exp Immunol. 2022 Jul 22;209(1):33-45. doi: 10.1093/cei/uxac029.

Abstract

The presence of tumour-infiltrating immune cells was originally associated with the induction of anti-tumour responses and good a prognosis. A more refined characterization of the tumour microenvironment has challenged this original idea and evidence now exists pointing to a critical role for immune cells in the modulation of anti-tumour responses and the induction of a tolerant pro-tumour environment. The coordinated action of diverse immunosuppressive populations, both innate and adaptive, shapes a variety of pro-tumour responses leading to tumour progression and metastasis. Regulatory B cells have emerged as critical modulators and suppressors of anti-tumour responses. As reported in autoimmunity and infection studies, Bregs are a heterogeneous population with diverse phenotypes and different mechanisms of action. Here we review recent studies on Bregs from animal models and patients, covering a variety of types of cancer. We describe the heterogeneity of Bregs, the cellular interactions they make with other immune cells and the tumour itself, and their mechanism of suppression that enables tumour escape. We also discuss the potential therapeutic tools that may inhibit Bregs function and promote anti-tumour responses.

摘要

肿瘤浸润免疫细胞的存在最初与抗肿瘤反应的诱导和良好的预后相关。对肿瘤微环境的更精细描述挑战了这一最初的观点,现在有证据表明,免疫细胞在调节抗肿瘤反应和诱导耐受的促肿瘤环境中起着关键作用。不同的先天和适应性免疫抑制群体的协调作用,形成了多种促进肿瘤进展和转移的促肿瘤反应。调节性 B 细胞已成为抗肿瘤反应的关键调节剂和抑制剂。正如在自身免疫和感染研究中报道的那样,Bregs 是一个异质性群体,具有不同的表型和不同的作用机制。在这里,我们综述了来自动物模型和患者的 Bregs 的最新研究,涵盖了多种类型的癌症。我们描述了 Bregs 的异质性、它们与其他免疫细胞和肿瘤本身的细胞相互作用以及它们抑制肿瘤逃逸的机制。我们还讨论了可能抑制 Bregs 功能并促进抗肿瘤反应的潜在治疗工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d38/9307227/9d67aea843b1/uxac029_fig3.jpg

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