Rosenberg Jacob M, Utz Paul J
Department of Medicine, Division of Immunology and Rheumatology, Stanford University School of Medicine , Stanford, CA , USA.
Department of Medicine, Division of Immunology and Rheumatology, Stanford University School of Medicine , Stanford, CA , USA ; Institute for Immunity, Transplantation, and Infection, Stanford University School of Medicine , Stanford, CA , USA.
Front Immunol. 2015 Apr 7;6:138. doi: 10.3389/fimmu.2015.00138. eCollection 2015.
Autoimmunity is highly coincident with immunodeficiency. In a small but growing number of primary immunodeficiencies, autoantibodies are diagnostic of a given disease and implicated in disease pathogenesis. In order to improve our understanding of the role of autoantibodies in immunodeficiencies and to discover novel autoantibodies, new proteomic tools are needed. Protein microarrays have the ability to screen for reactivity to hundreds to many thousands of unique autoantigens simultaneously on a single chip using minimal serum input. Here, we review different types of protein microarrays and how they can be useful in framing the study of primary and secondary immunodeficiencies.
自身免疫与免疫缺陷高度相关。在少数但数量不断增加的原发性免疫缺陷中,自身抗体可用于诊断特定疾病,并与疾病发病机制有关。为了更好地理解自身抗体在免疫缺陷中的作用并发现新的自身抗体,需要新的蛋白质组学工具。蛋白质微阵列能够在单个芯片上使用最少的血清输入同时筛选对数百至数千种独特自身抗原的反应性。在此,我们综述了不同类型的蛋白质微阵列以及它们如何有助于构建原发性和继发性免疫缺陷的研究。