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Potential roles of activation-induced cytidine deaminase in promotion or prevention of autoimmunity in humans

机译:激活诱导的胞苷脱氨酶在促进或预防人类自身免疫中的潜在作用

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摘要

Autoimmune manifestations are paradoxical and frequent complications of primary immunodeficiencies, including T and/or B cell defects. Among pure B cell defects, the Activation-induced cytidine Deaminase (AID)-deficiency, characterized by a complete lack of immunoglobulin class switch recombination and somatic hypermutation, is especially complicated by autoimmune disorders. We summarized in this review the different autoimmune and inflammatory manifestations present in 13 patients out of a cohort of 45 patients. Moreover, we also review the impact of AID mutations on B-cell tolerance and discuss hypotheses that may explain why central and peripheral B-cell tolerance was abnormal in the absence of functional AID. Hence, AID plays an essential role in controlling autoreactive B cells in humans and prevents the development of autoimmune syndromes.
机译:自身免疫表现是自发免疫缺陷的矛盾和常见并发症,包括T和/或B细胞缺陷。在纯B细胞缺陷中,以完全缺乏免疫球蛋白类别开关重组和体细胞高突变为特征的激活诱导的胞苷脱氨酶(AID)缺陷特别容易导致自身免疫疾病。我们在这篇综述中总结了45名患者中13名患者的不同自身免疫和炎症表现。此外,我们还审查了AID突变对B细胞耐受性的影响,并讨论了一些假设,这些假设可以解释为什么在缺乏功能性AID的情况下中枢和外周B细胞耐受性异常。因此,AID在控制人类自身反应性B细胞方面起着至关重要的作用,并可以防止自身免疫综合征的发展。

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