Characterization of viral dynamics in human immunodeficiency virus type 1-infected patients treated with combination antiretroviral therapy: Relationships to host factors, cellular restoration, and virologic end points

被引:94
作者
Wu, HL
Kuritzkes, DR
McClernon, DR
Kessler, H
Connick, E
Landay, A
Spear, G
Heath-Chiozzi, M
Rousseau, F
Fox, L
Spritzler, J
Leonard, JM
Lederman, MM
机构
[1] Frontier Sci & Technol Res Fdn Inc, Chestnut Hill, MA 02467 USA
[2] Harvard Univ, Sch Publ Hlth, Boston, MA 02115 USA
[3] Univ Colorado, Hlth Sci Ctr, Denver, CO USA
[4] Vet Affairs Med Ctr, Denver, CO USA
[5] Glaxo Wellcome Inc, Res Triangle Pk, NC 27709 USA
[6] Rush Presbyterian St Lukes Med Ctr, Chicago, IL 60612 USA
[7] Abbott Labs, Abbott Pk, IL 60064 USA
[8] NIAID, HIV Res Branch, Bethesda, MD 20892 USA
[9] Case Western Reserve Univ, Univ Hosp Cleveland, Cleveland, OH 44106 USA
关键词
D O I
10.1086/314670
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Biphasic plasma viral decays were modeled in 48 patients treated with ritonavir, zidovudine, and lamivudine, Estimated first- and second-phase decay rates were d(1) as 0.47/day and d(2) as 0.04/day. Interpatient differences in both decay rates were significant. The d(1) was directly correlated with baseline CD4(+), CD4(+)CD28(+), and CD8(+)CD28(+) T lymphocyte counts (P<.05) and inversely correlated with baseline virus load (P=.044) and the magnitude of CD4(+) and CD8(+) T lymphocyte recovery (P<.01). The d(2) was directly correlated with baseline percentage of CD8(+) T lymphocytes (P=.023), the CD8(+)CD38(+) cell number (P=.024), and the level of IgG that binds to human immunodeficiency virus (HIV) type 1 gp120 (P=.02), Viral decay rates were not predictive of treatment failure or durability of viral suppression. These exploratory findings are consistent with a model in which immunologic factors contribute to elimination of HIV-infected cells and suggest a dynamic interplay between regulation of HIV expression and lymphocyte activation and recovery.
引用
收藏
页码:799 / 807
页数:9
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