Centro de Desenvolvimento Científico e Tecnológico (CDCT), Fundação Estadual de Produção e Pesquisa em Saúde (FEPPS), Porto Alegre, Brazil. leonardo
J Clin Virol. 2012 May;54(1):6-10. doi: 10.1016/j.jcv.2012.01.005. Epub 2012 Feb 13.
Entry inhibitors are a class of antiretroviral (ARV) drugs that prevent HIV replication by blocking viral entry into the host cell. The investigation of naturally occurring mutations associated with entry inhibitors across subtypes is required because genetic differences between HIV-1 variants may influence the emergence of drug resistance. Despite the importance of subtype C, which predominates globally, the majority of studies include only subtype B strains.
To investigate the presence of natural resistance mutations to entry inhibitors in HIV-1 subtypes B, C, and CRF31_BC strains.
Eighty samples were collected from antiretroviral-naïve patients. The gp41 gene from 67 patients and the gp120 gene from 65 patients were partially sequenced. Resistance mutations to entry inhibitors Enfuvirtide, Maraviroc, and Vicriviroc were screened.
ENF resistance-associated mutations of HR1 and HR2 on gp41 were not associated with any subtype. However, the major polymorphisms detected in HR1: N42S, L54M, and A67T were most prevalent in subtype C (p<0.001). Mutations A316T and R315Q in gp120, which are related to MVC and VCV reduced susceptibility respectively, were predominant in subtype C (p<0.05).
This study shows that many more resistance-associated mutations to entry inhibitors in ARV-naïve patients occur in subtype C compared with subtype B strains. However, further studies will be necessary to elucidate if the differential genetic background of HIV subtypes can affect the efficacy of treatment with entry inhibitors.
进入抑制剂是一类抗逆转录病毒 (ARV) 药物,通过阻止病毒进入宿主细胞来阻止 HIV 复制。需要研究与进入抑制剂相关的自然发生的突变,因为 HIV-1 变体之间的遗传差异可能会影响耐药性的出现。尽管 C 亚型(全球主要亚型)很重要,但大多数研究仅包括 B 亚型株。
研究 HIV-1 B、C 和 CRF31_BC 亚型中进入抑制剂的天然耐药突变的存在情况。
从抗逆转录病毒初治患者中采集了 80 个样本。对 67 名患者的 gp41 基因和 65 名患者的 gp120 基因进行了部分测序。筛选了对进入抑制剂恩夫韦肽、马拉韦罗和维克瑞韦的耐药突变。
gp41 上 HR1 和 HR2 的 ENF 耐药相关突变与任何亚型均无关。然而,在 HR1 中检测到的主要多态性 N42S、L54M 和 A67T 最常见于 C 亚型(p<0.001)。与 MVC 和 VCV 分别相关的 gp120 上的突变 A316T 和 R315Q 主要见于 C 亚型(p<0.05)。
本研究表明,与 B 亚型株相比,在 ARV 初治患者中,许多与进入抑制剂相关的耐药突变更常见于 C 亚型。然而,需要进一步研究来阐明 HIV 亚型的不同遗传背景是否会影响进入抑制剂治疗的疗效。