Villano S A, Vlahov D, Nelson K E, Cohn S, Thomas D L
Division of Infectious Diseases, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Hepatology. 1999 Mar;29(3):908-14. doi: 10.1002/hep.510290311.
The purpose of this investigation was to prospectively characterize acute hepatitis C virus (HCV) infections and to evaluate the hypothesis that the outcome is affected by identifiable clinical or viral factors. One hundred forty-two people with a history of illicit drug use who were HCV antibody-negative in 1988 were followed semiannually through 1996. HCV seroconversion (second generation enzyme immunoassay and recombinant immunoblot assay) was recognized in 43 (30%) of the participants, who were followed up for a median of 72 months. HCV RNA was detected and quantified by polymerase chain reaction in a median of 10 specimens per participant and showed two distinct patterns of viremia: viral clearance was noted in 6 (14%) of the participants, and viral persistence was observed in 37 (86%) of the participants. Subjects with viral clearance were more likely to be white (P =.004), have jaundice (P =.03), and have lower peak viral titer (P =.003). However, the outcome for a given person could not be predicted by clinical features, RNA level, or HCV subtype (as ascertained by analysis of core-E1 complementary DNA sequence). No acute infections were recognized by health care providers. At the time of seroconversion, HCV RNA was detectable in 81% of participants, and recombinant immunoblot assay (RIBA) was positive in 85% of participants. We conclude that approximately 85% of people with acute hepatitis C develop persistent viremia. However, acute infections are uncommonly recognized clinically, underscoring the importance of screening individuals at risk. Long-term follow-up, but no single laboratory test, is necessary to ascertain the outcome and in some cases make the diagnosis of acute HCV infection.
本研究的目的是前瞻性地描述急性丙型肝炎病毒(HCV)感染情况,并评估结局受可识别的临床或病毒因素影响这一假设。1988年,142名有非法药物使用史且HCV抗体阴性的人每半年接受随访,直至1996年。43名(30%)参与者出现HCV血清学转换(第二代酶免疫测定和重组免疫印迹测定),这些参与者的随访中位时间为72个月。通过聚合酶链反应检测并定量每位参与者的HCV RNA,每位参与者的10份标本中值显示出两种不同的病毒血症模式:6名(14%)参与者出现病毒清除,37名(86%)参与者出现病毒持续存在。病毒清除的受试者更可能是白人(P = 0.004)、出现黄疸(P = 0.03)且病毒峰值滴度较低(P = 0.003)。然而,无法通过临床特征、RNA水平或HCV亚型(通过核心-E1互补DNA序列分析确定)预测特定个体的结局。医疗保健提供者未识别出任何急性感染。在血清学转换时,81%的参与者可检测到HCV RNA,85%的参与者重组免疫印迹测定(RIBA)呈阳性。我们得出结论,约85%的急性丙型肝炎患者会出现持续性病毒血症。然而,急性感染在临床上很少被识别,这凸显了对高危个体进行筛查的重要性。需要长期随访,但无需单一实验室检查来确定结局,在某些情况下进行急性HCV感染的诊断。