Weiler Catherine R, Bankers-Fulbright Jennifer L
Department of Internal Medicine and Division of Allergic Diseases, Mayo Clinic College of Medicine, Rochester, MN 55905, USA.
Mayo Clin Proc. 2005 Sep;80(9):1187-200. doi: 10.4065/80.9.1187.
Common variable immunodeficiency (CVID) is a primary immunodeficiency disorder that can present with multiple phenotypes, all of which are characterized by hypogammaglobulinemia, in a person at any age. A specific genetic defect that accounts for all CVID phenotypes has not been identified, and it is likely that several distinct genetic disorders with similar clinical presentations are responsible for the observed variation. In this review, we summarize the known genetic mutations that give rise to hypogammaglobulinemia and how these gene products affect normal or abnormal B-cell development and function, with particular emphasis on CVID. Additionally, we describe specific phenotypic and genetic laboratory tests that can be used to diagnose CVID and provide guidelines for test interpretation and subsequent therapeutic intervention.
普通可变免疫缺陷(CVID)是一种原发性免疫缺陷疾病,可在任何年龄的个体中表现出多种表型,所有这些表型均以低丙种球蛋白血症为特征。尚未确定导致所有CVID表型的特定遗传缺陷,观察到的变异可能是由几种具有相似临床表现的不同遗传疾病引起的。在本综述中,我们总结了已知的导致低丙种球蛋白血症的基因突变,以及这些基因产物如何影响正常或异常的B细胞发育和功能,特别强调了CVID。此外,我们描述了可用于诊断CVID的特定表型和基因实验室检测,并提供检测结果解读及后续治疗干预的指导原则。