HIV-1潜伏的机制及其治疗意义

A. Sanyaolu, D. Hammoudi, O. Badaru, Ifeoluwa Adekanye, Adeola Akinwekomi, Kateryna Shyshkova
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引用次数: 0

摘要

在接受高效抗逆转录病毒治疗(HAART)的患者中,静止HIV-1在CD4+ T细胞中的潜伏期是病毒完全破坏的障碍。这种潜伏期在急性感染早期出现,但在宿主细胞中保持沉默;然而,如果停止抗病毒治疗,它仍然能够制造感染性原病毒。HAART治疗的目标是将感染者血清中HIV-1的复制水平降低到检测不到的水平。HIV-1的治疗涉及使用多种药物,因为这种病毒很容易获得对抑制剂的耐药性。由于HIV-1基因组在几个个体内的多样性而产生耐药性。基因治疗方法已被证明在某种程度上更安全,但尚未在人体模型中得到证实。HIV-1潜伏的过程是多因素的,涉及几个仍在研究中的分子途径。本研究综述了HIV-1潜伏期及其治疗意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Mechanism of HIV-1 Latency and Therapeutic Implication
The latency of resting HIV-1 in CD4+ T cells is the obstacle to complete destruction of the virus in patients that have been given highly active antiretroviral therapy (HAART). This latency occurs early during acute infection but remains silent in the host cells; however it is still capable of making infectious proviruses if antiviral therapy is stopped. The goal of HAART therapy is to reduce the replication levels of HIV-1 to undetectable levels in serum of infected individuals. HIV-1 therapy involves the use of multiple drugs because of the ability of the virus to easily acquire drug resistance to an inhibitor. Resistance develops due to the diversity of HIV-1 genome within several individuals. Gene therapy approaches have been shown to be somewhat safer but have not been proven yet in human models. The process of HIV-1 latency is multifactorial and involves several molecular pathways which are still being studied. This study reviews HIV-1 latency as well as its therapeutic implication.
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