McGill University AIDS Centre, Jewish General Hospital, 3755 Cote-Ste-Catherine Road, Montreal, Quebec, H3T 1E2, Canada; E-Mail:
Viruses. 2010 Nov;2(11):2493-508. doi: 10.3390/v2112493. Epub 2010 Nov 11.
Despite the fact that over 90% of HIV-1 infected people worldwide harbor non-subtype B variants of HIV-1, knowledge of resistance mutations in non-B HIV-1 and their clinical relevance is limited. Due to historical delays in access to antiretroviral therapy (ART) on a worldwide basis, the vast majority of reports on drug resistance deal with subtype B infections in developed countries. However, both enzymatic and virological data support the concept that naturally occurring polymorphisms among different nonB subtypes can affect HIV-1 susceptibility to antiretroviral drugs (ARVs), the magnitude of resistance conferred by major mutations, and the propensity to acquire some resistance mutations. Tools need to be optimized to assure accurate measurements of drug susceptibility of non-B subtypes. Furthermore, there is a need to recognize that each subtype may have a distinct resistance profile and that differences in resistance pathways may also impact on cross-resistance and the selection of second-line regimens. It will be essential to pay attention to newer drug combinations in well designed long-term longitudinal studies involving patients infected by viruses of different subtypes.
尽管全球超过 90%的 HIV-1 感染者携带非 B 型 HIV-1 变异株,但对非 B 型 HIV-1 中的耐药突变及其临床意义的了解有限。由于在全球范围内获得抗逆转录病毒治疗 (ART) 的时间滞后,大多数耐药性报告都涉及发达国家的 B 型感染。然而,酶学和病毒学数据都支持这样一种观点,即不同非 B 型之间的自然发生的多态性会影响 HIV-1 对抗逆转录病毒药物 (ARV) 的敏感性、主要突变赋予的耐药程度以及获得某些耐药突变的倾向。需要优化工具以确保对非 B 型的药物敏感性进行准确测量。此外,还需要认识到每个亚型可能具有独特的耐药谱,并且耐药途径的差异也可能影响交叉耐药性和二线方案的选择。在涉及不同亚型病毒感染患者的精心设计的长期纵向研究中,关注新的药物组合将至关重要。