Qadir Muhammad Imran, Zafar Maria
Institute of Molecular Biology & Biotechnology, Bahauddin Zakariya University, Multan, Pakistan.
Department of Pharmacy, Quaid-i-Azam University, Islamabad, Pakistan.
Crit Rev Eukaryot Gene Expr. 2017;27(3):237-246. doi: 10.1615/CritRevEukaryotGeneExpr.2017019418.
HIV infection presents a major community health hazard, partially because the HIV virus is capable of evading antiretroviral therapies. Most anti-HIV drugs were intended to target virus-encoded mechanisms; however, some host-encoded molecules comparatively execute a vital role in the life cycle of virus. Thus, these might be considered as target sites for antiviral agents. TSG101 is important among these antiviral therapies because, as a cytoplasmic molecule, it facilitates viral budding and release. In this review, HIV-infected cells have TSG101 on their surface and thus can be used in antibody-based therapies. The development of a monoclonal antibody CB8-2 lessens the assembly of viruses from infected cells. This mechanism represents the potential use of TSG101-directed antibodies to fight against AIDS.
艾滋病毒感染对社区健康构成重大危害,部分原因是艾滋病毒能够逃避抗逆转录病毒疗法。大多数抗艾滋病毒药物旨在针对病毒编码的机制;然而,一些宿主编码分子在病毒生命周期中发挥着至关重要的作用。因此,这些分子可能被视为抗病毒药物的靶点。TSG101在这些抗病毒疗法中很重要,因为作为一种细胞质分子,它促进病毒出芽和释放。在本综述中,感染艾滋病毒的细胞表面有TSG101,因此可用于基于抗体的治疗。单克隆抗体CB8-2的开发减少了受感染细胞中病毒的组装。这种机制代表了TSG101导向抗体在抗击艾滋病方面的潜在用途。