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从巨噬细胞储存库中根除慢病毒的当前及未来治疗策略

Current and Future Therapeutic Strategies for Lentiviral Eradication from Macrophage Reservoirs.

作者信息

Peterson Tiffany A, MacLean Andrew G

机构信息

Division of Comparative Pathology, Tulane National Primate Research Center, Covington, LA, USA.

Department of Microbiology & Immunology, Division of Comparative Pathology, Tulane National Primate Research Center, Tulane Center for Aging, Tulane Brain Institute, 18703 Three Rivers Road, Covington, LA, 70433, USA.

出版信息

J Neuroimmune Pharmacol. 2019 Mar;14(1):68-93. doi: 10.1007/s11481-018-9814-5. Epub 2018 Oct 13.

DOI:10.1007/s11481-018-9814-5
PMID:30317409
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6391209/
Abstract

Macrophages, one of the most abundant populations of leukocytes in the body, function as the first line of defense against pathogen invaders. Human Immunodeficiency virus 1 (HIV-1) remains to date one of the most extensively studied viral infections. Naturally occurring lentiviruses in domestic and primate species serve as valuable models to investigate lentiviral pathogenesis and novel therapeutics. Better understanding of the role macrophages play in HIV pathogenesis will aid in the advancement towards a cure. Even with current efficacy of first- and second-line Antiretroviral Therapy (ART) guidelines and future efficacy of Long Acting Slow Effective Release-ART (LASER-ART); ART alone does not lead to a cure. The major challenge of HIV eradication is viral latency. Latency Reversal Agents (LRAs) show promise as a possible means to eradicate HIV-1 from the body. It has become evident that complete eradication will need to include combinations of various effective therapeutic strategies such as LASER-ART, LRAs, and gene editing. Review of the current literature indicates the most promising HIV eradication strategy appears to be LASER-ART in conjunction with viral and receptor gene modifications via the CRISPR/Cas9 system. Graphical abstract A multimodal approach to HIV treatment including gene editing, LASER-ART, and latency reversal agents may provide a means to achieve HIV eradication.

摘要

巨噬细胞是体内最丰富的白细胞群体之一,作为抵御病原体入侵的第一道防线发挥作用。人类免疫缺陷病毒1(HIV-1)至今仍是研究最为广泛的病毒感染之一。家畜和灵长类动物中天然存在的慢病毒是研究慢病毒发病机制和新型疗法的宝贵模型。更好地了解巨噬细胞在HIV发病机制中的作用将有助于推动治愈方法的进展。即使有目前一线和二线抗逆转录病毒疗法(ART)指南的疗效以及长效缓释抗逆转录病毒疗法(LASER-ART)未来的疗效;仅靠抗逆转录病毒疗法并不能治愈。根除HIV的主要挑战是病毒潜伏。潜伏逆转剂(LRA)有望成为从体内根除HIV-1的一种可能手段。显而易见,彻底根除需要包括LASER-ART、LRA和基因编辑等各种有效治疗策略的组合。对当前文献的综述表明,最有前景的HIV根除策略似乎是LASER-ART结合通过CRISPR/Cas9系统对病毒和受体基因进行修饰。图形摘要 一种包括基因编辑、LASER-ART和潜伏逆转剂的多模式HIV治疗方法可能提供实现根除HIV的手段。