Sneller M C, Strober W, Eisenstein E, Jaffe J S, Cunningham-Rundles C
Laboratory of Immunoregulation, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892.
Ann Intern Med. 1993 May 1;118(9):720-30. doi: 10.7326/0003-4819-118-9-199305010-00011.
Common variable immunodeficiency (CVI) is a heterogenous immunodeficiency syndrome characterized by hypogammaglobulinemia, recurrent bacterial infections, and various immunologic abnormalities. In addition to recurrent infections, patients with this syndrome also have an increased incidence of autoimmune disease and malignancy. Because the spectrum of associated diseases is broad, patients with CVI are seen by various medical specialists. This review discusses the pathogenesis, clinical manifestations, diagnosis, and treatment of CVI.
普通可变免疫缺陷(CVI)是一种异质性免疫缺陷综合征,其特征为低丙种球蛋白血症、反复细菌感染以及各种免疫异常。除反复感染外,该综合征患者患自身免疫性疾病和恶性肿瘤的发生率也增加。由于相关疾病谱广泛,CVI患者会由不同医学专科医生诊治。本文综述讨论了CVI的发病机制、临床表现、诊断和治疗。