Coen D M
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115.
Ann N Y Acad Sci. 1990;616:224-37. doi: 10.1111/j.1749-6632.1990.tb17843.x.
Antiviral drug resistance is an area of increasing importance in acquired immunodeficiency syndrome (AIDS), not only in terms of the human immunodeficiency virus (HIV), but also opportunistic pathogens such as herpes simplex virus (HSV) and human cytomegalovirus (CMV). Studies of drug resistance in these and other viruses have proven valuable both for the molecular dissection of drug mechanisms and drug targets and for predicting the features of drug resistance in clinical settings: Drug-resistance mutations arise readily, due in part to a lack of fidelity of viral polymerase. Both biochemical and genetic analyses are generally required to understand the basis of drug resistance. Novel drug targets, such as a CMV gene product that contributes to ganciclovir phosphorylation, can be identified by analysis of such mutations. Regions of drug targets that are involved in drug recognition can be identified by sequencing of drug-resistance mutations. Analysis of drug-resistant viruses, obtained either in the laboratory or from patients, reveals a broad spectrum of alterations and points to the importance of heterogeneous populations of virus in resistance and pathogenesis.
抗病毒药物耐药性在获得性免疫缺陷综合征(AIDS)中是一个日益重要的领域,不仅涉及人类免疫缺陷病毒(HIV),还包括机会性病原体,如单纯疱疹病毒(HSV)和人巨细胞病毒(CMV)。对这些病毒及其他病毒的耐药性研究已证明,其对于药物作用机制和药物靶点的分子剖析,以及预测临床环境中的耐药特征均具有重要价值:耐药突变易于出现,部分原因是病毒聚合酶缺乏保真度。通常需要生化和遗传学分析来理解耐药性的基础。通过对这类突变的分析,可以识别出新的药物靶点,例如一种有助于更昔洛韦磷酸化的CMV基因产物。通过对耐药突变进行测序,可以确定药物靶点中参与药物识别的区域。对在实验室中获得或从患者身上分离出的耐药病毒进行分析,揭示了广泛的变异,并指出病毒异质群体在耐药性和发病机制中的重要性。