Klinik für Immunologie und Rheumatologie, Medizinische Hochschule Hannover (MHH), Carl-Neuberg Straße 1, D-30625 Hannover, Germany.
Centre for Chronic Immunodeficiency, University Medical Centre, University of Freiburg, Faculty of Medicine, Breisacher Straße 115, D-79106 Freiburg, Germany.
Nat Rev Rheumatol. 2017 Dec 19;14(1):7-18. doi: 10.1038/nrrheum.2017.198.
Autoimmunity and immunodeficiency were previously considered to be mutually exclusive conditions; however, increased understanding of the complex immune regulatory and signalling mechanisms involved, coupled with the application of genetic analysis, is revealing the complex relationships between primary immunodeficiency syndromes and autoimmune diseases. Single-gene defects can cause rare diseases that predominantly present with autoimmune symptoms. Such genetic defects also predispose individuals to recurrent infections (a hallmark of immunodeficiency) and can cause primary immunodeficiencies, which can also lead to immune dysregulation and autoimmunity. Moreover, risk factors for polygenic rheumatic diseases often exist in the same genes as the mutations that give rise to primary immunodeficiency syndromes. In this Review, various primary immunodeficiency syndromes are presented, along with their pathogenetic mechanisms and relationship to autoimmune diseases, in an effort to increase awareness of immunodeficiencies that occur concurrently with autoimmune diseases and to highlight the need to initiate appropriate genetic tests. The growing knowledge of various genetically determined pathologic mechanisms in patients with immunodeficiencies who have autoimmune symptoms opens up new avenues for personalized molecular therapies that could potentially treat immunodeficiency and autoimmunity at the same time, and that could be further explored in the context of autoimmune rheumatic diseases.
自身免疫和免疫缺陷以前被认为是相互排斥的条件;然而,对涉及的复杂免疫调节和信号机制的深入了解,加上遗传分析的应用,揭示了原发性免疫缺陷综合征和自身免疫性疾病之间的复杂关系。单基因缺陷可导致主要表现为自身免疫症状的罕见疾病。这种遗传缺陷也使个体易患复发性感染(免疫缺陷的标志),并可导致原发性免疫缺陷,这也可导致免疫失调和自身免疫。此外,多基因风湿性疾病的危险因素通常存在于与导致原发性免疫缺陷综合征的突变相同的基因中。在这篇综述中,介绍了各种原发性免疫缺陷综合征,以及它们的发病机制与自身免疫性疾病的关系,旨在提高对与自身免疫性疾病同时发生的免疫缺陷的认识,并强调需要进行适当的基因检测。对有自身免疫症状的免疫缺陷患者中各种遗传决定的病理机制的不断深入了解,为同时治疗免疫缺陷和自身免疫开辟了新途径,并且可以在自身免疫性风湿性疾病的背景下进一步探索。