Reassessing the Human Immunodeficiency Virus Type 1 Life Cycle through Age-Structured Modeling: Life Span of Infected Cells, Viral Generation Time, and Basic Reproductive Number, R0

被引:39
作者
Althaus, Christian L. [1 ]
De Vos, Anneke S. [1 ]
De Boer, Rob J. [1 ]
机构
[1] Univ Utrecht, NL-3584 CH Utrecht, Netherlands
关键词
HIV-1; INFECTION; IN-VIVO; ANTIRETROVIRAL THERAPY; INTRACELLULAR DELAY; LOAD DATA; DYNAMICS; LIMITATIONS; CLEARANCE; DEATH;
D O I
10.1128/JVI.01799-08
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The rapid decay of the viral load after drug treatment in patients infected with human immunodeficiency virus type 1 (HIV-1) has been shown to result from the rapid loss of infected cells due to their high turnover, with a generation time of around 1 to 2 days. Traditionally, viral decay dynamics after drug treatment is investigated using models of differential equations in which both the death rate of infected cells and the viral production rate are assumed to be constant. Here, we describe age-structured models of the viral decay dynamics in which viral production rates and death rates depend on the age of the infected cells. In order to investigate the effects of age-dependent rates, we compared these models with earlier descriptions of the viral load decay and fitted them to previously published data. We have found no supporting evidence that infected-cell death rates increase, but cannot reject the possibility that viral production rates increase, with the age of the cells. In particular, we demonstrate that an exponential increase in viral production with infected-cell age is perfectly consistent with the data. Since an exponential increase in virus production can compensate for the exponential loss of infected cells, the death rates of HIV-1-infected cells may be higher than previously anticipated. We discuss the implications of these findings for the life span of infected cells, the viral generation time, and the basic reproductive number, R-0.
引用
收藏
页码:7659 / 7667
页数:9
相关论文
共 26 条
  • [1] Target cell limited and immune control models of HIV infection: A comparison
    De Boer, RJ
    Perelson, AS
    [J]. JOURNAL OF THEORETICAL BIOLOGY, 1998, 190 (03) : 201 - 214
  • [2] Dixit NM, 2004, ANTIVIR THER, V9, P237
  • [3] Modelling cell lifespan and proliferation: is likelihood to die or to divide independent of age?
    Dowling, MR
    Milutinovic, D
    Hodgkin, PD
    [J]. JOURNAL OF THE ROYAL SOCIETY INTERFACE, 2005, 2 (05) : 517 - 526
  • [4] HIV replication elicits little cytopathic effects little cytopathic effects in vivo:: Analysis of surrogate markers for virus production, cytotoxic T cell response and infected cell death
    Funk, Georg A.
    Oxenius, Annette
    Fischer, Marek
    Opravil, Milos
    Joos, Beda
    Flepp, Markus
    Weber, Rainer
    Guenthard, Huldrych F.
    Bonhoeffer, Sebastian
    [J]. JOURNAL OF MEDICAL VIROLOGY, 2006, 78 (09) : 1141 - 1146
  • [5] Optimizing within-host viral fitness: infected cell lifespan and virion production rate
    Gilchrist, MA
    Coombs, D
    Perelson, AS
    [J]. JOURNAL OF THEORETICAL BIOLOGY, 2004, 229 (02) : 281 - 288
  • [6] Gompertz B., 1825, PHILOS T ROY SOC LON, V115, P513, DOI [10.1098/rstl.1825.0026, DOI 10.1098/RSTL.1825.0026]
  • [7] VISNA DNA-SYNTHESIS AND THE TEMPO OF INFECTION INVITRO
    HAASE, AT
    STOWRING, L
    HARRIS, JD
    TRAYNOR, B
    VENTURA, P
    PELUSO, R
    BRAHIC, M
    [J]. VIROLOGY, 1982, 119 (02) : 399 - 410
  • [8] Viral dynamics in vivo: Limitations on estimates of intracellular delay and virus decay
    Herz, AVM
    Bonhoeffer, S
    Anderson, RM
    May, RM
    Nowak, MA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (14) : 7247 - 7251
  • [9] RAPID TURNOVER OF PLASMA VIRIONS AND CD4 LYMPHOCYTES IN HIV-1 INFECTION
    HO, DD
    NEUMANN, AU
    PERELSON, AS
    CHEN, W
    LEONARD, JM
    MARKOWITZ, M
    [J]. NATURE, 1995, 373 (6510) : 123 - 126
  • [10] The HIV-1 vaccine race
    Ho, DD
    Huang, YX
    [J]. CELL, 2002, 110 (02) : 135 - 138