D Urbano Vanessa, De Crignis Elisa, Re Maria Carla
Retrovirus Laboratory, Operative Unit of Clinical Microbiology, S. Orsola-Malpighi University Hospital, Bologna, Italy.
Curr HIV Res. 2018;16(3):184-207. doi: 10.2174/1570162X16666180817115830.
Mammalian cells have evolved several mechanisms to prevent or block lentiviral infection and spread. Among the innate immune mechanisms, the signaling cascade triggered by type I interferon (IFN) plays a pivotal role in limiting the burden of HIV-1. In the presence of IFN, human cells upregulate the expression of a number of genes, referred to as IFN-stimulated genes (ISGs), many of them acting as antiviral restriction factors (RFs). RFs are dominant proteins that target different essential steps of the viral cycle, thereby providing an early line of defense against the virus. The identification and characterization of RFs have provided unique insights into the molecular biology of HIV-1, further revealing the complex host-pathogen interplay that characterizes the infection. The presence of RFs drove viral evolution, forcing the virus to develop specific proteins to counteract their activity. The knowledge of the mechanisms that prevent viral infection and their viral counterparts may offer new insights to improve current antiviral strategies. This review provides an overview of the RFs targeting HIV-1 replication and the mechanisms that regulate their expression as well as their impact on viral replication and the clinical course of the disease.
哺乳动物细胞已经进化出多种机制来预防或阻止慢病毒感染和传播。在先天免疫机制中,I型干扰素(IFN)触发的信号级联反应在限制HIV-1负担方面起着关键作用。在IFN存在的情况下,人类细胞会上调许多基因的表达,这些基因被称为IFN刺激基因(ISG),其中许多基因作为抗病毒限制因子(RF)发挥作用。RF是主要蛋白质,靶向病毒周期的不同关键步骤,从而提供针对病毒的早期防御线。RF的鉴定和表征为HIV-1的分子生物学提供了独特的见解,进一步揭示了表征感染的复杂宿主-病原体相互作用。RF的存在推动了病毒进化,迫使病毒产生特定蛋白质来对抗它们的活性。了解预防病毒感染的机制及其病毒对应物可能为改进当前抗病毒策略提供新的见解。本综述概述了靶向HIV-1复制的RF、调节其表达的机制以及它们对病毒复制和疾病临床进程的影响。