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 1010 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 (t1/2) of 3.7 ± 1.2 d, similar to the t1/2 observed in the noncytolytic clearance of covalently closed circular DNA for other hepadnaviruses. The final phase of virion clearance occurs at a variable rate (t1/2 of 4.8 to 284 d) and may relate to the rate of loss of infected hepatocytes. Free virus has a mean t1/2 of at most 1.2 ± 0.6 d. We estimate a peak HBV production rate of at least 1013 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.
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2 April 2001
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April 02 2001
Kinetics of Acute Hepatitis B Virus Infection in Humans
Simon A. Whalley,
Simon A. Whalley
aCentre for Hepatology, Department of Medicine, Royal Free Campus,
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John M. Murray,
John M. Murray
cTheoretical Division, Los Alamos National Laboratory, Los Alamos, New Mexico 87545
dSchool of Mathematics, University of New South Wales, Sydney NSW 2052, Australia
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Dave Brown,
Dave Brown
aCentre for Hepatology, Department of Medicine, Royal Free Campus,
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George J.M. Webster,
George J.M. Webster
aCentre for Hepatology, Department of Medicine, Royal Free Campus,
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Vincent C. Emery,
Vincent C. Emery
bDepartment of Virology, Royal Free and University College Medical School, London NW3 2QG, United Kingdom
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Geoffrey M. Dusheiko,
Geoffrey M. Dusheiko
aCentre for Hepatology, Department of Medicine, Royal Free Campus,
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Alan S. Perelson
Alan S. Perelson
cTheoretical Division, Los Alamos National Laboratory, Los Alamos, New Mexico 87545
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Simon A. Whalley
aCentre for Hepatology, Department of Medicine, Royal Free Campus,
John M. Murray
cTheoretical Division, Los Alamos National Laboratory, Los Alamos, New Mexico 87545
dSchool of Mathematics, University of New South Wales, Sydney NSW 2052, Australia
Dave Brown
aCentre for Hepatology, Department of Medicine, Royal Free Campus,
George J.M. Webster
aCentre for Hepatology, Department of Medicine, Royal Free Campus,
Vincent C. Emery
bDepartment of Virology, Royal Free and University College Medical School, London NW3 2QG, United Kingdom
Geoffrey M. Dusheiko
aCentre for Hepatology, Department of Medicine, Royal Free Campus,
Alan S. Perelson
cTheoretical Division, Los Alamos National Laboratory, Los Alamos, New Mexico 87545
Abbreviations used in this paper: ALT, alanine transaminase; ccc, covalently closed circular; DHBV, duck HBV; HBV, hepatitis B virus; HBsAg, hepatitis B surface antigen; IS, internal standard.
Received:
October 11 2000
Accepted:
February 26 2001
Online ISSN: 1540-9538
Print ISSN: 0022-1007
© 2001 The Rockefeller University Press
2001
The Rockefeller University Press
J Exp Med (2001) 193 (7): 847–854.
Article history
Received:
October 11 2000
Accepted:
February 26 2001
Citation
Simon A. Whalley, John M. Murray, Dave Brown, George J.M. Webster, Vincent C. Emery, Geoffrey M. Dusheiko, Alan S. Perelson; Kinetics of Acute Hepatitis B Virus Infection in Humans. J Exp Med 2 April 2001; 193 (7): 847–854. doi: https://doi.org/10.1084/jem.193.7.847
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