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目前对人类调节性B细胞(Bregs)的表型和功能特性的理解。

The current understanding of the phenotypic and functional properties of human regulatory B cells (Bregs).

作者信息

Ahsan Nawara Faiza, Lourenço Stella, Psyllou Dimitra, Long Alexander, Shankar Sushma, Bashford-Rogers Rachael

机构信息

Department of Biochemistry, University of Oxford, Oxford OX1 3QU, United Kingdom.

Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, United Kingdom.

出版信息

Oxf Open Immunol. 2024 Sep 20;5(1):iqae012. doi: 10.1093/oxfimm/iqae012. eCollection 2024.

DOI:10.1093/oxfimm/iqae012
PMID:39346706
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11427547/
Abstract

B cells can have a wide range of pro- and anti- inflammatory functions. A subset of B cells called regulatory B cells (Bregs) can potently suppress immune responses. Bregs have been shown to maintain immune homeostasis and modulate inflammatory responses. Bregs are an exciting cellular target across a range of diseases, including Breg induction in autoimmunity, allergy and transplantation, and Breg suppression in cancers and infection. Bregs exhibit a remarkable phenotypic heterogeneity, rendering their unequivocal identification a challenging task. The lack of a universally accepted and exclusive surface marker set for Bregs across various studies contributes to inconsistencies in their categorization. This review paper presents a comprehensive overview of the current understanding of the phenotypic and functional properties of human Bregs while addressing the persisting ambiguities and discrepancies in their characterization. Finally, the paper examines the promising therapeutic opportunities presented by Bregs as their immunomodulatory capacities have gained attention in the context of autoimmune diseases, allergic conditions, and cancer. We explore the exciting potential in harnessing Bregs as potential therapeutic agents and the avenues that remain open for the development of Breg-based treatment strategies.

摘要

B细胞可具有广泛的促炎和抗炎功能。一类被称为调节性B细胞(Bregs)的B细胞亚群能够有效抑制免疫反应。研究表明,Bregs可维持免疫稳态并调节炎症反应。在一系列疾病中,Bregs都是令人关注的细胞靶点,包括在自身免疫性疾病、过敏和移植中诱导Bregs,以及在癌症和感染中抑制Bregs。Bregs表现出显著的表型异质性,这使得明确鉴定它们成为一项具有挑战性的任务。在各种研究中,缺乏一套普遍接受且唯一的Bregs表面标志物,这导致了它们分类的不一致性。本文综述全面概述了目前对人类Bregs表型和功能特性的理解,同时解决了其特征描述中持续存在的模糊性和差异。最后,鉴于Bregs的免疫调节能力在自身免疫性疾病、过敏性疾病和癌症背景下受到关注,本文探讨了Bregs带来的有前景的治疗机会。我们探索了将Bregs作为潜在治疗剂的令人兴奋的潜力,以及基于Bregs的治疗策略开发仍有待开拓的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a21b/11427547/7805f60b708f/iqae012f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a21b/11427547/b254c291529a/iqae012f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a21b/11427547/a91a2fb3bd19/iqae012f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a21b/11427547/7805f60b708f/iqae012f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a21b/11427547/b254c291529a/iqae012f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a21b/11427547/a91a2fb3bd19/iqae012f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a21b/11427547/7805f60b708f/iqae012f3.jpg

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2
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Nature. 2023 Jul;619(7969):348-356. doi: 10.1038/s41586-023-06231-0. Epub 2023 Jun 21.
3
CAR T Cell Therapy: A Versatile Living Drug.嵌合抗原受体 T 细胞疗法:一种多功能活体药物。
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Front Immunol. 2025 Apr 8;16:1561171. doi: 10.3389/fimmu.2025.1561171. eCollection 2025.
4
Tumor secretome shapes the immune landscape during cancer progression.肿瘤分泌组在癌症进展过程中塑造免疫格局。
J Exp Clin Cancer Res. 2025 Feb 10;44(1):47. doi: 10.1186/s13046-025-03302-0.
Int J Mol Sci. 2023 Mar 27;24(7):6300. doi: 10.3390/ijms24076300.
4
Pancreatic cancer: Emerging field of regulatory B-cell-targeted immunotherapies.胰腺癌:调控性 B 细胞靶向免疫治疗的新兴领域。
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