Morris A, Webster A D, Brown D, Harrison T J, Dusheiko G
Department of Clinical Immunology, Medical Research Council Immunodeficiency Clinic, Royal Free Hospital, London, United Kingdom.
J Infect Dis. 1998 Jun;177(6):1719-22. doi: 10.1086/517430.
Sera from 77 patients with common variable immunodeficiency (CVID) were tested for GB virus C (GBV-C) RNA, because they are prone to unexplained chronic hepatitis, and from 28 patients with X-linked agammaglobulinemia (XLA) who have a similar primary antibody deficiency but are not prone to hepatitis. Eight CVID and 8 XLA patients were positive; 6 positive CVID and 3 XLA patients had abnormal liver enzymes, explained in 3 by either hepatitis B or C virus infection. Most patients tested had antibodies to the E2 antigen of GBV-C, apparently passively acquired from their immunoglobulin therapy. The high prevalence of GBV-C viremia in CVID and XLA patients is probably explained by their long-term exposure to blood products. Our data indicate that GBV-C does not cause chronic hepatitis in immunocompromised XLA patients and is not the cause of chronic non-B or -C hepatitis in the majority of CVID patients.
对77例普通可变免疫缺陷(CVID)患者的血清进行了GB病毒C(GBV-C)RNA检测,因为他们易患不明原因的慢性肝炎,还检测了28例X连锁无丙种球蛋白血症(XLA)患者的血清,这些患者有类似的原发性抗体缺陷,但不易患肝炎。8例CVID患者和8例XLA患者检测结果呈阳性;6例CVID阳性患者和3例XLA阳性患者肝功能酶异常,其中3例由乙型或丙型肝炎病毒感染所致。大多数接受检测的患者体内有针对GBV-C E2抗原的抗体,显然是从免疫球蛋白治疗中被动获得的。CVID和XLA患者中GBV-C病毒血症的高流行率可能是由于他们长期接触血液制品所致。我们的数据表明,GBV-C不会在免疫功能低下的XLA患者中引起慢性肝炎,也不是大多数CVID患者慢性非B或非C型肝炎的病因。