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治疗性B细胞耗竭可识别免疫调节网络。

Therapeutic B cell depletion identifies immunoregulatory networks.

作者信息

Polonio Carolina M, Quintana Francisco J

机构信息

Ann Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.

Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA.

出版信息

J Clin Invest. 2025 Jun 2;135(11). doi: 10.1172/JCI189442.

Abstract

B cell depletion is a highly effective therapy in multiple sclerosis (MS), reducing inflammation and restoring immune balance. In this issue of the JCI, Wei et al. used single-cell RNA-Seq and flow cytometry, identifying the comprehensive effects of B cell depletion on the immune response, including an increase in antiinflammatory cerebrospinal fluid macrophages and elevated TNF-α expression by peripheral CD16+ monocytes. The authors also detected shifts in T cell populations that resulted in reduced myelin-reactive CD4+ T cells and the expansion of TIGIT+ Tregs. The findings uncover immunoregulatory mechanisms and suggest therapeutic strategies for MS and other autoimmune disorders.

摘要

B细胞耗竭是治疗多发性硬化症(MS)的一种高效疗法,可减轻炎症并恢复免疫平衡。在本期《临床研究杂志》中,Wei等人使用单细胞RNA测序和流式细胞术,确定了B细胞耗竭对免疫反应的全面影响,包括抗炎性脑脊液巨噬细胞增加以及外周CD16+单核细胞的TNF-α表达升高。作者还检测到T细胞群体的变化,导致髓鞘反应性CD4+ T细胞减少以及TIGIT+调节性T细胞(Tregs)扩增。这些发现揭示了免疫调节机制,并为MS和其他自身免疫性疾病提出了治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e94/12126224/93dfa01fd1c8/jci-135-189442-g095.jpg

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