Poveda Eva, Briz Verónica, Soriano Vincent
Department of Infectious Diseases, Hospital Carlos III, Madrid, Spain.
AIDS Rev. 2005 Jul-Sep;7(3):139-47.
Entry inhibitors are a new class of drugs for the treatment of HIV infection. Enfuvirtide is the first compound of this family to be approved for clinical use. It blocks HIV fusion to host cells. It is a synthetic peptide that mimics an HR2 fragment of gp41, blocking the formation of a six-helix bundle structure which is critical in the fusion process. Enfuvirtide is a good therapeutic option as rescue therapy in combination with other active antiretrovirals and works against different HIV-1 variants, including all group M subtypes and group O. However, it is not active against HIV-2. The main mechanism of resistance to enfuvirtide depends of the selection of changes in a 10-amino acid domain between residues 36 to 45 in the HR1 region of gp41. Single and double mutations in this region have been shown to result in high-level resistance to enfuvirtide. A negative impact of enfuvirtide-resistance mutations on viral fitness has been postulated, since resistance mutations tend to disappear soon after drug discontinuation and because immunologic benefits have been noticed despite virologic failure in patients undergoing enfuvirtide treatment.
进入抑制剂是一类用于治疗HIV感染的新型药物。恩夫韦肽是该类药物中首个被批准用于临床的化合物。它可阻断HIV与宿主细胞的融合。它是一种合成肽,模拟gp41的HR2片段,阻止六螺旋束结构的形成,而该结构在融合过程中至关重要。恩夫韦肽作为与其他活性抗逆转录病毒药物联合使用的挽救疗法是一种很好的治疗选择,并且对不同的HIV-1变体有效,包括所有M组亚型和O组。然而,它对HIV-2无活性。对恩夫韦肽耐药的主要机制取决于gp41的HR1区域中36至45位残基之间10个氨基酸结构域变化的选择。该区域的单突变和双突变已被证明会导致对恩夫韦肽的高水平耐药。有人推测恩夫韦肽耐药突变对病毒适应性有负面影响,因为耐药突变在停药后往往很快消失,并且尽管接受恩夫韦肽治疗的患者出现病毒学失败,但仍观察到了免疫学益处。