Sjögren综合征B细胞表型、免疫球蛋白基因表达异常及自身免疫的出现。

Arthritis Research Pub Date : 2002-01-01 Epub Date: 2002-09-25 DOI:10.1186/ar603
Thomas Dörner, Peter E Lipsky
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引用次数: 48

摘要

原发性Sjögren综合征(pSS)是一种自身免疫性疾病,以特定的病理特征和产生典型的自身抗体为特征。此外,外周B细胞亚群分布的特征性变化和免疫球蛋白可变区基因使用的差异也是pSS的特征。将pSS患者的血液和腮腺中的B细胞与正常供体的B细胞进行比较,表明外周血中的记忆B细胞减少,这些抗原经历的B细胞在腮腺中积累或保留。由于无序选择导致这些患者的B细胞库存在相当大的差异,因此对其性质的描述将为这种自身免疫性炎症疾病的发病机制提供重要的进一步线索。
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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Abnormalities of B cell phenotype, immunoglobulin gene expression and the emergence of autoimmunity in Sjögren's syndrome.

Primary Sjögren's syndrome (pSS) is an autoimmune disorder characterized by specific pathologic features and the production of typical autoantibodies. In addition, characteristic changes in the distribution of peripheral B cell subsets and differences in use of immunoglobulin variable-region genes are also features of pSS. Comparison of B cells from the blood and parotid gland of patients with pSS with those of normal donors suggests that there is a depletion of memory B cells from the peripheral blood and an accumulation or retention of these antigen-experienced B cells in the parotids. Because disordered selection leads to considerable differences in the B cell repertoire in these patients, the delineation of its nature should provide important further clues to the pathogenesis of this autoimmune inflammatory disorder.

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