首页> 外文期刊>International archives of allergy and immunology >Autoimnriunity in Primary Antibody Deficiencies
【24h】

Autoimnriunity in Primary Antibody Deficiencies

机译:原发性抗体缺乏症的自动免疫

获取原文
获取原文并翻译 | 示例
           

摘要

Primary antibody deficiencies (PADs) are the most common inherited primary immunodeficiencies in humans, characterized by hypogammaglobulinemia, an inability to produce specific antibodies, and recurrent infections mainly caused by encapsulated bacteria. However, it has been shown that inflammatory disorders, granulomatous lesions, lymphoproliferative diseases, cancer, and autoimnnunity are associated with the various types of PAD. Both systemic and organ-specific autoimmune diseases could be attributed to B-cell defects in PAD patients. Immune thrombocytopenic purpura and autoimmune hemolytic anemia are the most common autoimmune disorders in this group of patients. The aim of this review is to describe the proposed mechanisms for autoimmunity and to review the literature with respect to the reported autoimmune disorders in each type of PAD. (C) 2016 S. Karger AG, Basel
机译:原发性抗体缺陷症(PAD)是人类最常见的遗传性原发性免疫缺陷症,其特征是低球蛋白球蛋白血症,无法产生特异性抗体以及主要由封装细菌引起的反复感染。然而,已经表明,炎性疾病,肉芽肿性病变,淋巴增生性疾病,癌症和自身免疫性与各种PAD有关。全身性和器官特异性自身免疫性疾病均可归因于PAD患者的B细胞缺陷。免疫性血小板减少性紫癜和自身免疫性溶血性贫血是该组患者中最常见的自身免疫性疾病。这篇综述的目的是描述提出的自身免疫机制,并回顾关于每种PAD类型中报道的自身免疫疾病的文献。 (C)2016 S.Karger AG,巴塞尔

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号