Chinniah Romona, Adimulam Theolan, Nandlal Louansha, Arumugam Thilona, Ramsuran Veron
Centre for the AIDS Programme of Research in South Africa (CAPRISA), University of KwaZulu-Natal, Durban, South Africa.
School of Laboratory Medicine and Medical Sciences, University of KwaZulu-Natal, Durban, South Africa.
Front Genet. 2022 May 4;13:862642. doi: 10.3389/fgene.2022.862642. eCollection 2022.
Over many years, research on HIV/AIDS has advanced with the introduction of HAART. Despite these advancements, significant gaps remain with respect to aspects in HIV life cycle, with specific attention to virus-host interactions. Investigating virus-host interactions may lead to the implementation of novel therapeutic strategies against HIV/AIDS. Notably, host gene silencing can be facilitated by cellular small non-coding RNAs such as microRNAs paving the way for epigenetic anti-viral therapies. Numerous studies have elucidated the importance of microRNAs in HIV pathogenesis. Some microRNAs can either promote viral infection, while others can be detrimental to viral replication. This is accomplished by targeting the HIV-proviral genome or by regulating host genes required for viral replication and immune responses. In this review, we report on 1) the direct association of microRNAs with HIV infection; 2) the indirect association of known human genetic factors with HIV infection; 3) the regulation of human genes by microRNAs in other diseases that can be explored experimentally to determine their effect on HIV-1 infection; and 4) therapeutic interactions of microRNA against HIV infection.
多年来,随着高效抗逆转录病毒疗法(HAART)的引入,对艾滋病毒/艾滋病的研究取得了进展。尽管有这些进展,但在艾滋病毒生命周期的各个方面仍存在重大差距,尤其在病毒与宿主的相互作用方面。研究病毒与宿主的相互作用可能会带来针对艾滋病毒/艾滋病的新型治疗策略。值得注意的是,细胞小非编码RNA(如微小RNA)可促进宿主基因沉默,为表观遗传抗病毒疗法铺平了道路。众多研究阐明了微小RNA在艾滋病毒发病机制中的重要性。一些微小RNA可促进病毒感染,而另一些则可能对病毒复制有害。这是通过靶向艾滋病毒前病毒基因组或通过调节病毒复制和免疫反应所需的宿主基因来实现的。在本综述中,我们报告了:1)微小RNA与艾滋病毒感染的直接关联;2)已知人类遗传因素与艾滋病毒感染的间接关联;3)微小RNA在其他疾病中对人类基因的调控,可通过实验探索以确定其对HIV-1感染的影响;以及4)微小RNA针对艾滋病毒感染的治疗相互作用。