Williams Carolyn F, Klinzman Donna, Yamashita Traci E, Xiang Jinhua, Polgreen Philip M, Rinaldo Charles, Liu Chenglong, Phair John, Margolick Joseph B, Zdunek Dietmar, Hess Georg, Stapleton Jack T
Epidemiology Branch, Division of AIDS, National Institute of Allergy and Infectious Diseases, Bethesda, Md, USA.
N Engl J Med. 2004 Mar 4;350(10):981-90. doi: 10.1056/NEJMoa030107.
GB virus C (GBV-C), which is not known to be pathogenic in humans, replicates in lymphocytes, inhibits the replication of human immunodeficiency virus (HIV) in vitro, and has been associated with a decreased risk of death among HIV-positive persons in some, but not all, studies. Previous studies did not control for differences in the duration of HIV or GBV-C infection.
We evaluated 271 men who were participants in the Multicenter Acquired Immunodeficiency Syndrome Cohort Study for GBV-C viremia (by means of a reverse-transcriptase-polymerase-chain-reaction assay) or E2 antibody (by means of an enzyme-linked immunosorbent assay) 12 to 18 months after seroconversion to positivity for HIV (the early visit); a subgroup of 138 patients was also evaluated 5 to 6 years after HIV seroconversion (the late visit).
GBV-C infection was detected in 85 percent of men with HIV seroconversion on the basis of the presence of E2 antibody (46 percent) or GBV-C RNA (39 percent). Only one man acquired GBV-C viremia between the early and the late visit, but 9 percent of men had clearance of GBV-C RNA between these visits. GBV-C status 12 to 18 months after HIV seroconversion was not significantly associated with survival; however, men without GBV-C RNA 5 to 6 years after HIV seroconversion were 2.78 times as likely to die as men with persistent GBV-C viremia (95 percent confidence interval, 1.34 to 5.76; P=0.006). The poorest prognosis was associated with the loss of GBV-C RNA (relative hazard for death as compared with men with persistent GBV-C RNA, 5.87; P=0.003).
GBV-C viremia was significantly associated with prolonged survival among HIV-positive men 5 to 6 years after HIV seroconversion, but not at 12 to 18 months, and the loss of GBV-C RNA by 5 to 6 years after HIV seroconversion was associated with the poorest prognosis. Understanding the mechanisms of interaction between GBV-C and HIV may provide insight into the progression of HIV disease.
丙型肝炎病毒GB病毒C型(GBV-C)在人类中不具有致病性,可在淋巴细胞中复制,在体外可抑制人类免疫缺陷病毒(HIV)复制,并且在一些(但并非所有)研究中,GBV-C感染与HIV阳性者死亡风险降低有关。既往研究未对HIV或GBV-C感染持续时间的差异进行控制。
我们对参加多中心获得性免疫缺陷综合征队列研究的271名男性进行了评估,在其HIV血清转化呈阳性后12至18个月(早期访视)检测GBV-C病毒血症(采用逆转录-聚合酶链反应法)或E2抗体(采用酶联免疫吸附测定法);还对138名患者的亚组在HIV血清转化后5至6年进行了评估(晚期访视)。
根据E2抗体(46%)或GBV-C RNA(39%)的存在情况,在85%的HIV血清转化男性中检测到GBV-C感染。在早期和晚期访视之间,只有1名男性出现GBV-C病毒血症,但9%的男性在这两次访视期间GBV-C RNA清除。HIV血清转化后12至18个月时的GBV-C状态与生存无显著相关性;然而,HIV血清转化后5至6年时无GBV-C RNA的男性死亡可能性是持续存在GBV-C病毒血症男性的2.78倍(95%置信区间为1.34至5.76;P = 0.006)。预后最差与GBV-C RNA消失有关(与持续存在GBV-C RNA的男性相比,死亡相对风险为5.87;P = 0.003)。
GBV-C病毒血症与HIV血清转化后5至6年的HIV阳性男性长期生存显著相关,但在12至18个月时并非如此,并且HIV血清转化后5至6年GBV-C RNA消失与预后最差有关。了解GBV-C与HIV之间的相互作用机制可能有助于深入了解HIV疾病的进展。