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病毒表型和基因型作为临床试验中的标志物。

Viral phenotype and genotype as markers in clinical trials.

作者信息

Katzenstein D A

机构信息

Center for AIDS Research, Stanford University Medical Center, CA 94305, USA.

出版信息

J Acquir Immune Defic Syndr Hum Retrovirol. 1995;10 Suppl 2:S25-34.

PMID:7552510
Abstract

Treatment of AIDS and HIV infection is increasingly dependent on the use of surrogate markers to assess the efficacy of drug and biologic therapies in individual patients and in the clinical trials. Recent developments in laboratory techniques have resulted in new assays to measure circulating viral RNA in HIV-infected individuals, standardized methods to assess genotypic changes in virus associated with drug resistance and biologic assays for syncytia-inducing phenotype, a viral characteristic associated with rapid clinical progression. Studies from our laboratory have examined the relationship between surrogate markers of drug efficacy, CD4 cell changes, quantitative HIV plasma RNA and cell dilution cultures, genotypic changes associated with drug resistance and the syncytia-inducing phenotype. The results of these studies suggest that drug-resistance genotype and syncytia-inducing phenotype are independent factors that contribute to disease progression in patients receiving zidovudine. The design of studies of drugs and biologics for the treatment of HIV should include assessment of genotypic and phenotypic characteristics of HIV in addition to CD4 cell numbers and virus load.

摘要

艾滋病和艾滋病毒感染的治疗越来越依赖于使用替代指标来评估药物和生物疗法在个体患者以及临床试验中的疗效。实验室技术的最新进展带来了新的检测方法,用于测量艾滋病毒感染者体内循环的病毒RNA,评估与耐药性相关的病毒基因型变化的标准化方法,以及针对诱导融合表型(一种与临床快速进展相关的病毒特征)的生物检测方法。我们实验室的研究考察了药物疗效替代指标、CD4细胞变化、艾滋病毒血浆RNA定量与细胞稀释培养之间的关系,以及与耐药性和诱导融合表型相关的基因型变化。这些研究结果表明,耐药基因型和诱导融合表型是导致接受齐多夫定治疗的患者疾病进展的独立因素。用于治疗艾滋病毒的药物和生物制剂的研究设计,除了CD4细胞数量和病毒载量外,还应包括对艾滋病毒基因型和表型特征的评估。

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