HIV-1 infection and low steady state viral loads

被引:319
作者
Callaway, DS
Perelson, AS
机构
[1] Los Alamos Natl Lab, Los Alamos, NM 87545 USA
[2] Cornell Univ, Dept Theoret & Appl Mech, Ithaca, NY 14853 USA
关键词
D O I
10.1006/bulm.2001.0266
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Highly active antiretroviral therapy (HAART) reduces the viral burden in human immunodeficiency virus type 1 (HIV-1) infected patients below the threshold of detectability. However, substantial evidence indicates that viral replication persists in these individuals. In this paper we examine the ability of several biologically motivated models of HIV-1 dynamics to explain sustained low viral loads. At or near drug efficacies that result in steady state viral loads below detectability, most models are extremely sensitive to small changes in drug efficacy. We argue that if these models reflect reality many patients should have cleared the virus, contrary to observation. We find that a model in which the infected cell death rate is dependent on the infected cell density does not suffer this shortcoming. The shortcoming is also overcome in two more conventional models that include small populations of cells in which the drug is less effective than in the main population, suggesting that difficulties with drug penetrance and maintenance of effective intracellular drug concentrations in all cells susceptible to HIV infection may underlie ongoing viral replication. (C) 2002 Society for Mathematical Biology.
引用
收藏
页码:29 / 64
页数:36
相关论文
共 56 条
[41]  
Puddu P, 1999, LAB INVEST, V79, P1299
[42]   The decay of the latent reservoir of replication-competent HIV-1 is inversely correlated with the extent of residual viral replication during prolonged anti-retroviral therapy [J].
Ramratnam, B ;
Mittler, JE ;
Zhang, LQ ;
Boden, D ;
Hurley, A ;
Fang, F ;
Macken, CA ;
Perelson, AS ;
Markowitz, M ;
Ho, DD .
NATURE MEDICINE, 2000, 6 (01) :82-85
[43]   Rapid production and clearance of HIV-1 and hepatitis C virus assessed by large volume plasma apheresis [J].
Ramratnam, B ;
Bonhoeffer, S ;
Binley, J ;
Hurley, A ;
Zhang, LQ ;
Mittler, JE ;
Markowitz, M ;
Moore, JP ;
Perelson, AS ;
Ho, DD .
LANCET, 1999, 354 (9192) :1782-1785
[44]   Turnover of CD4+ and CD8+ T lymphocytes in HIV-1 infection as measured by Ki-67 antigen [J].
Sachsenberg, N ;
Perelson, AS ;
Yerly, S ;
Schockmel, GA ;
Leduc, D ;
Hirschel, B ;
Perrin, L .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 187 (08) :1295-1303
[45]  
Schlegel P CS, 1998, CAMPBELLS UROLOGY, V7, P1254
[46]   Persistence of episomal HIV-1 infection intermediates in patients on highly active anti-retroviral therapy [J].
Sharkey, ME ;
Teo, I ;
Greenough, T ;
Sharova, N ;
Luzuriaga, K ;
Sullivan, JL ;
Bucy, RP ;
Kostrikis, LG ;
Haase, A ;
Veryard, C ;
Davaro, RE ;
Cheeseman, SH ;
Daly, JS ;
Bova, C ;
Ellison, RT ;
Mady, B ;
Lai, KK ;
Moyle, G ;
Nelson, M ;
Gazzard, B ;
Shaunak, S ;
Stevenson, M .
NATURE MEDICINE, 2000, 6 (01) :76-81
[47]   Latency and viral persistence in HIV-1 infection [J].
Siliciano, JD ;
Siliciano, RF .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 106 (07) :823-825
[48]   Persistence of infectious HIV on follicular dendritic cells [J].
Smith, BA ;
Gartner, S ;
Liu, YL ;
Perelson, AS ;
Stilianakis, NI ;
Keele, BF ;
Kerkering, TM ;
Ferreira-Gonzalez, A ;
Szakal, AK ;
Tew, JG ;
Burton, GF .
JOURNAL OF IMMUNOLOGY, 2001, 166 (01) :690-696
[49]   ROLE OF THE HTLV-III/LAV ENVELOPE IN SYNCYTIUM FORMATION AND CYTOPATHICITY [J].
SODROSKI, J ;
GOH, WC ;
ROSEN, C ;
CAMPBELL, K ;
HASELTINE, WA .
NATURE, 1986, 322 (6078) :470-474
[50]   Portals of entry: Uncovering HIV nuclear transport pathways [J].
Stevenson, M .
TRENDS IN CELL BIOLOGY, 1996, 6 (01) :9-15