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Antiretroviral drug resistance in non-subtype B HIV-1, HIV-2 and SIV.

机译:非亚型B HIV-1,HIV-2和SIV的抗逆转录病毒药物耐药性。

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摘要

Patients infected with HIV-1 of subtype other than B ('non-subtype B') or with HIV-2 are being treated with antiretroviral drugs in increasing numbers. In addition, healthcare providers and laboratory workers working with clinical specimens or animals infected with HIV, SIV or SHIV are at risk of being exposed to the virus and might require post-exposure prophylactic treatment. Thus, it is important to understand the inherent antiviral susceptibility of non-subtype B HIV-1, HIV-2 and SIV to currently available antiretroviral drugs, which have been developed with subtype B HIV-1-infected patients as the primary target population. In addition, knowledge about the consequences of treatment failure in non-subtype B HIV-1- and HIV-2-infected patients, with respect to the development of drug resistance, is crucial for designing optimal treatment strategies. This review summarizes the current state of knowledge in these areas. Non-subtype B group M HIV-1 appears to be susceptible to available agents, but follows several unique pathways to resistance to some drugs that have important clinical implications. Group O HIV-1 is naturally resistant to the non-nucleoside reverse transcriptase inhibitors (NNRTIs). HIV-2 and SIVsm are also naturally resistant to the NNRTIs as well as the protease inhibitor amprenavir. More research into the clinical responses to existing drugs and interpretation of genotypic information is needed, as well as development of diagnostic assays specific for non-subtype B HIV-1 and HIV-2.
机译:正在接受越来越多的抗逆转录病毒药物治疗的感染了非B亚型HIV-1(非B亚型)或HIV-2的患者。此外,与感染了HIV,SIV或SHIV的临床标本或动物打交道的医疗保健提供者和实验室工作人员有暴露于病毒的风险,可能需要暴露后的预防性治疗。因此,重要的是要了解非B型HIV-1,HIV-2和SIV对目前可用的抗逆转录病毒药物的固有抗病毒敏感性,这些药物已经以B型HIV-1感染的患者作为主要目标人群而开发。另外,关于抗药性发展方面的知识,对于非B型HIV-1和HIV-2感染亚型患者的治疗失败的后果,对于设计最佳治疗策略至关重要。这篇综述总结了这些领域的当前知识状态。非B亚型M组HIV-1似乎对现有药物敏感,但遵循几种独特的途径对某些具有重要临床意义的药物产生抗药性。 O型HIV-1对非核苷类逆转录酶抑制剂(NNRTIs)具有天然抗性。 HIV-2和SIVsm以及蛋白酶抑制剂安普那韦也对NNRTIs具有天然抗性。需要对现有药物的临床反应和基因型信息的解释进行更多研究,并需要开发针对非B型HIV-1和HIV-2的诊断分析方法。

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