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在未接受过抗逆转录病毒治疗的患者中,基线HIV-1 RNA水平和CD4细胞计数可预测对奈非那韦病毒学应答丧失的时间,但不能预测对洛匹那韦/利托那韦病毒学应答丧失的时间。

Baseline HIV-1 RNA level and CD4 cell count predict time to loss of virologic response to nelfinavir, but not lopinavir/ritonavir, in antiretroviral therapy-naive patients.

作者信息

King Martin S, Bernstein Barry M, Walmsley Sharon L, Sherer Renslow, Feinberg Judith, Sanne Ian, Cernohous Paul, Montaner Julio S G, Brun Scott C, Sun Eugene

机构信息

Abbott Laboratories, Abbott Park, Illinois, USA.

出版信息

J Infect Dis. 2004 Jul 15;190(2):280-4. doi: 10.1086/422037. Epub 2004 Jun 11.

Abstract

Baseline CD4 cell counts and human immunodeficiency virus (HIV)-1 RNA levels have been shown to predict immunologic and virologic responses in HIV-infected patients receiving antiretroviral therapy. In our randomized, double-blind, comparative trial, 653 antiretroviral therapy-naive patients received lopinavir/ritonavir or nelfinavir, plus stavudine and lamivudine, for up to 96 weeks. The risk of loss of virologic response was significantly higher for nelfinavir-treated patients than for lopinavir/ritonavir-treated patients (Cox model hazard ratio, 2.2; 95% confidence interval, 1.7-3.0; P<.001). For nelfinavir-treated patients, but not for lopinavir/ritonavir-treated patients, higher baseline HIV-1 RNA levels and lower baseline CD4 cell counts were associated with a higher risk of loss of virologic response.

摘要

基线CD4细胞计数和人类免疫缺陷病毒(HIV)-1 RNA水平已被证明可预测接受抗逆转录病毒治疗的HIV感染患者的免疫和病毒学反应。在我们的随机、双盲、对照试验中,653例初治抗逆转录病毒治疗患者接受洛匹那韦/利托那韦或奈非那韦,加司他夫定和拉米夫定,治疗长达96周。奈非那韦治疗的患者病毒学反应丧失的风险显著高于洛匹那韦/利托那韦治疗的患者(Cox模型风险比,2.2;95%置信区间,1.7 - 3.0;P<0.001)。对于奈非那韦治疗的患者,而非洛匹那韦/利托那韦治疗的患者,较高的基线HIV-1 RNA水平和较低的基线CD4细胞计数与病毒学反应丧失的较高风险相关。

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