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抗中性粒细胞胞浆抗体相关性血管炎中的抗髓过氧化物酶IgM B细胞

Anti-myeloperoxidase IgM B cells in anti-neutrophil cytoplasmic antibody-associated vasculitis.

作者信息

Wortel C M, van de Wetering R, Stork E M, Kissel T, Reijm S, van der Woude D, van Schie K A, Trouw L A, Teng Yko, Rutgers A, Heeringa P, Voll R E, Rizzi M, Venhoff N, Toes Rem, Scherer H U

机构信息

Department of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.

Department of Immunology, Leiden University Medical Center, Leiden, The Netherlands.

出版信息

Nat Commun. 2025 Feb 12;16(1):1582. doi: 10.1038/s41467-025-56786-x.

Abstract

Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is a prototypic autoimmune disease, with a subset of AAV patients manifesting anti-myeloperoxidase (MPO) IgG. Patients with AAV respond positively to B cell-targeting and complement-targeting therapies, but disease flares are not uncommon. Here, by comparing samples from healthy individuals and MPO AVV patients, we show that B cell autoreactivity against MPO in the circulation of patients is dominated by CD27IgM B cells whereas MPO-specific IgG cells are infrequent. Additionally, while naive anti-MPO-IgM B cells are present in both patients and controls and produce anti-MPO IgM upon stimulation, anti-MPO-IgM memory B cells and serum anti-MPO IgM are features of patients. Our results thus hint that defective elimination of B cell reactivity to MPO in the human repertoire, the presence of activated IgM anti-MPO B cells in disease, and a dominant role for anti-MPO IgM in complement activation, may all contribute to MPO AAV etiology and thereby serve as potential target for therapy.

摘要

抗中性粒细胞胞浆抗体(ANCA)相关血管炎(AAV)是一种典型的自身免疫性疾病,部分AAV患者表现出抗髓过氧化物酶(MPO)IgG。AAV患者对靶向B细胞和靶向补体的疗法反应良好,但疾病复发并不罕见。在此,通过比较健康个体和MPO AAV患者的样本,我们发现患者循环中针对MPO的B细胞自身反应性以CD27IgM B细胞为主,而MPO特异性IgG细胞很少见。此外,虽然患者和对照组中均存在初始抗MPO-IgM B细胞,且在刺激后产生抗MPO IgM,但抗MPO-IgM记忆B细胞和血清抗MPO IgM是患者的特征。因此,我们的结果提示,人类免疫库中对MPO的B细胞反应性消除缺陷、疾病中活化的IgM抗MPO B细胞的存在以及抗MPO IgM在补体激活中的主导作用,可能都有助于MPO AAV的病因形成,从而成为潜在的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af43/11822119/e95d40354060/41467_2025_56786_Fig1_HTML.jpg

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