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关于肠道微生物群-B细胞-IgA轴及IgA肾病治疗的新思考

New thoughts on the intestinal microbiome-B cell-IgA axis and therapies in IgA nephropathy.

作者信息

Dang Shaoqing, Zhang Xiangyu, Zhang Yuemiao, Zhang Hong

机构信息

Renal Division, Department of Medicine, Peking University First Hospital, Beijing, China; Institute of Nephrology, Peking University, Beijing, China; Key Laboratory of Renal Disease, Ministry of Health of China, Beijing, China; Key Laboratory of Chronic Kidney Disease Prevention and Treatment (Peking University), Ministry of Education, Beijing, China; Research Units of Diagnosis and Treatment of Immune-mediated Kidney Diseases, Chinese Academy of Medical Sciences, Beijing, China.

Renal Division, Department of Medicine, Peking University First Hospital, Beijing, China; Institute of Nephrology, Peking University, Beijing, China; Key Laboratory of Renal Disease, Ministry of Health of China, Beijing, China; Key Laboratory of Chronic Kidney Disease Prevention and Treatment (Peking University), Ministry of Education, Beijing, China; Research Units of Diagnosis and Treatment of Immune-mediated Kidney Diseases, Chinese Academy of Medical Sciences, Beijing, China.

出版信息

Autoimmun Rev. 2025 Jul 31;24(8):103835. doi: 10.1016/j.autrev.2025.103835. Epub 2025 May 11.

DOI:10.1016/j.autrev.2025.103835
PMID:40360014
Abstract

IgA nephropathy (IgAN), as the most common chronic glomerulonephritis worldwide, is often triggered by mucosal infections and follows a chronic progression, with the majority of patients ultimately progressing to end-stage renal disease (ESRD) during their lifetimes. Since the mystery of its complete pathogenesis has not been fully solved, the resulting lack of effective early diagnosis and treatment greatly affects the prognosis of patients. Given the well-defined pathological feature of IgA deposition in the mesangial region, the source and role of pathogenic IgA has been focused on. Starting from the microbiology and immunity of the gut, we systematically review both the physiological and the pathological process of microbiome-B cell-IgA axis, from microbial-induced IgA production to the role of IgA in the intestinal immune milieu, and ultimately end up with the various aspects of microbiome-B cell-IgA axis in the pathogenesis of IgAN as well as the corresponding therapeutic initiatives available. Our retrospective review helps researchers to systematically understand the complex role between intestinal flora dysbiosis and pathogenic IgA in IgAN. This understanding provides a foundation for in-depth explorations to uncover more detailed pathogenic mechanisms and to develop more precise and effective diagnostic and therapeutic approaches.

摘要

IgA肾病(IgAN)是全球最常见的慢性肾小球肾炎,常由黏膜感染引发,并呈慢性进展,大多数患者最终会在一生中发展为终末期肾病(ESRD)。由于其完整发病机制的谜团尚未完全解开,因此缺乏有效的早期诊断和治疗方法,这极大地影响了患者的预后。鉴于系膜区IgA沉积这一明确的病理特征,致病性IgA的来源和作用一直是研究重点。从肠道微生物学和免疫学出发,我们系统回顾了微生物群-B细胞-IgA轴的生理和病理过程,从微生物诱导的IgA产生到IgA在肠道免疫环境中的作用,最终阐述了微生物群-B细胞-IgA轴在IgAN发病机制中的各个方面以及相应的治疗措施。我们的回顾性综述有助于研究人员系统地了解肠道菌群失调与致病性IgA在IgAN中的复杂作用。这种理解为深入探索以揭示更详细的致病机制以及开发更精确有效的诊断和治疗方法奠定了基础。

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引用本文的文献

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Front Pharmacol. 2025 Jul 30;16:1559593. doi: 10.3389/fphar.2025.1559593. eCollection 2025.