Johnson V A
Department of Medicine, University of Alabama at Birmingham 35294-0006.
J Infect Dis. 1995 Mar;171 Suppl 2:S140-9. doi: 10.1093/infdis/171.supplement_2.s140.
Drug-resistant isolates of human immunodeficiency virus type 1 (HIV-1) emerge during long-term treatment with nucleoside reverse transcriptase inhibitors, such as zidovudine. The clinical significance of in vitro drug resistance to zidovudine has been difficult to determine. However, in a virologic analysis of baseline specimens from the AIDS Clinical Trials Group (ACTG) 116B/117 study, high-level zidovudine resistance, defined as an IC50 of > or = 1 microM at study entry, was significantly associated with clinical disease progression. High-level zidovudine resistance also was an independent predictor of death as an end point, although this finding does not imply a direct causal effect. Duration and cumulative dose of prior zidovudine therapy did not predict clinical disease progression. More potent antiretroviral agents are needed that can be used in combination to achieve more complete virus suppression and to reduce the selection of drug-resistant HIV-1 mutants.
在使用核苷类逆转录酶抑制剂(如齐多夫定)进行长期治疗期间,会出现1型人类免疫缺陷病毒(HIV-1)的耐药分离株。体外对齐多夫定耐药的临床意义一直难以确定。然而,在艾滋病临床试验组(ACTG)116B/117研究的基线标本病毒学分析中,高水平的齐多夫定耐药(定义为研究开始时IC50≥1微摩尔)与临床疾病进展显著相关。高水平的齐多夫定耐药也是以死亡为终点的独立预测因素,尽管这一发现并不意味着存在直接因果效应。既往齐多夫定治疗的持续时间和累积剂量并不能预测临床疾病进展。需要更有效的抗逆转录病毒药物,可联合使用以实现更完全的病毒抑制,并减少耐药HIV-1突变体的产生。