包涵体肌炎患者肌肉组织中的浆细胞浸润物具有不同的B细胞受体再灌注特性。

Roy Jiang, Bhaskar Roy, Qian Wu, Subhasis Mohanty, Richard J Nowak, Albert C Shaw, Steven H Kleinstein, Kevin C O'Connor
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摘要

包涵体肌炎(IBM)是一种自身免疫性和退行性骨骼肌疾病。IBM肌肉组织中的B细胞浸润主要是完全分化的分泌Ab的浆细胞,很少有幼稚或记忆性B细胞。这种浸润在疾病病理中的作用尚不清楚。为了更好地定义IBM的体液反应,我们使用人类来源标本的适应性免疫受体库测序,从IBM肌肉活检中生成大型BCR库,并将其与皮肌炎、多发性肌炎和循环CD27+记忆B细胞生成的BCR库进行比较,这些细胞来源于健康对照和接种疫苗后收集的Ab分泌细胞。IBM浸润的细胞库特性包括:在大小上等于或超过高度克隆的疫苗相关Ab分泌细胞库的克隆;CDR和框架区中体细胞突变选择压力降低;以及使用具有少量表达IgM的细胞群的类别转换IgG和IgA同种型。表达IBM IgM的群体显示出独特的特征,包括体细胞突变频率升高和CDR3的独特物理化学性质。这些发现表明,IBM肌肉BCR的一些特征与皮肌炎、多发性肌炎和循环Ag经历亚群不同,这表明它可能是通过疾病特异性Ag的选择形成的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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The Plasma Cell Infiltrate Populating the Muscle Tissue of Patients with Inclusion Body Myositis Features Distinct B Cell Receptor Repertoire Properties.

Inclusion body myositis (IBM) is an autoimmune and degenerative disorder of skeletal muscle. The B cell infiltrates in IBM muscle tissue are predominantly fully differentiated Ab-secreting plasma cells, with scarce naive or memory B cells. The role of this infiltrate in the disease pathology is not well understood. To better define the humoral response in IBM, we used adaptive immune receptor repertoire sequencing, of human-derived specimens, to generate large BCR repertoire libraries from IBM muscle biopsies and compared them to those generated from dermatomyositis, polymyositis, and circulating CD27+ memory B cells, derived from healthy controls and Ab-secreting cells collected following vaccination. The repertoire properties of the IBM infiltrate included the following: clones that equaled or exceeded the highly clonal vaccine-associated Ab-secreting cell repertoire in size; reduced somatic mutation selection pressure in the CDRs and framework regions; and usage of class-switched IgG and IgA isotypes, with a minor population of IgM-expressing cells. The IBM IgM-expressing population revealed unique features, including an elevated somatic mutation frequency and distinct CDR3 physicochemical properties. These findings demonstrate that some of IBM muscle BCR repertoire characteristics are distinct from dermatomyositis and polymyositis and circulating Ag-experienced subsets, suggesting that it may form through selection by disease-specific Ags.

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