[Development of autoimmunity in patients with primary immunodeficiencies].

Práxedes Chiunti-Andrade, Carlos Arturo Gallardo-Hernández, Sandra Luz González-Herrera
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Abstract

The autoimmune diseases include many in which the immune system is directed against the host, leading to life-threatening destruction of organs. The origin of autoimmune disorders can be multifactorial and, there are no specific therapy for these diseases. Primary immunodeficiencies are a group of immune disorders that affect different components of the innate and adaptive responses. Interestingly, patients with primary immunodeficiencies have an increased susceptibility to infectious diseases and non-infectious complications including allergies, malignancies, and autoimmune diseases. The molecular mechanism for development of autoimmunity in immunodeficiencies is unclear. The study of the complex immune regulatory and signaling mechanisms is revealing the relationships between primary immunodeficiency syndromes and autoimmune diseases. Newly, it has been demonstrated that a deficient maturation of immune cells; the deficiency of proteins important for T and B lymphocyte function and impaired signally pathways that include key molecules in regulation and activation of immune cells are associated with the development of autoimmunity in patients with primary immunodeficiencies. The aim of the present work is to review the evidence available to date regarding the cellular and molecular mechanisms involved in the development of autoimmunity in patients with primary immunodeficiencies.

Abstract Image

【原发性免疫缺陷患者自身免疫的发展】。
自身免疫性疾病包括许多免疫系统直接针对宿主,导致危及生命的器官破坏。自身免疫性疾病的起源可以是多因素的,并且没有针对这些疾病的特异性治疗方法。原发性免疫缺陷是一组免疫紊乱,影响先天和适应性反应的不同组成部分。有趣的是,原发性免疫缺陷患者对感染性疾病和非感染性并发症(包括过敏、恶性肿瘤和自身免疫性疾病)的易感性增加。免疫缺陷患者自身免疫发生的分子机制尚不清楚。复杂的免疫调节和信号机制的研究揭示了原发性免疫缺陷综合征与自身免疫性疾病之间的关系。最近,已经证明免疫细胞成熟缺陷;原发性免疫缺陷患者自身免疫的发展与T和B淋巴细胞功能重要蛋白的缺乏以及包括调节和激活免疫细胞的关键分子在内的信号通路受损有关。本研究的目的是回顾迄今为止有关原发性免疫缺陷患者自身免疫发展的细胞和分子机制的证据。
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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