Kinetics of acute hepatitis B virus infection in humans

被引:142
作者
Whalley, SA
Murray, JM
Brown, D
Webster, GJM
Emery, VC
Dusheiko, GM
Perelson, AS
机构
[1] Los Alamos Natl Lab, Div Theoret, Los Alamos, NM 87545 USA
[2] UCL Royal Free & Univ Coll Med Sch, Dept Virol, London NW3 2QG, England
[3] UCL Royal Free & Univ Coll Med Sch, Dept Med, Ctr Hepatol, London NW3 2QG, England
[4] Univ New S Wales, Sch Math, Sydney, NSW 2052, Australia
关键词
acute hepatitis B; kinetics; cytotoxic T lymphocytes; mutation; hepatocyte;
D O I
10.1084/jem.193.7.847
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Using patient data from a unique single source outbreak of hepatitis B virus (HBV) infection, we have characterized the kinetics of acute HBV infection by monitoring viral turnover in the serum during the late incubation and clinical phases of the disease in humans. HBV replicates rapidly with minimally estimated doubling times ranging between 2.2 and 5.8 d (mean 3.7 +/- 1.5 d), After a peak viral load in serum of nearly 10(10) HBV DNA copies/ml is attained, clearance of HBV DNA follows a two or three phase decay pattern with an initial rapid decline characterized by mean half-life (t(1/2)) of 3.7 +/- 1.2 d, similar to the t(1/2) observed in the noncytolytic clearance of covalently closed circular DNA for other hepadnaviruses. The final phase of virion clearance occurs at a variable rate (t(1/2) of 4.8 to 284 d) and may relate to the rate of loss of infected hepatocytes. Free virus has a mean t(1/2) of at most 1.2 +/- 0.6 d. We estimate a peak HBV production rate of at least 10(13) virions/day and a maximum production rate of an infected hepatocyte of 200-1,000 virions/day, on average. At this peak rate of virion production we estimate that every possible single and most double mutations would be created each day.
引用
收藏
页码:847 / 853
页数:7
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