Lady Davis Institute, Jewish General Hospital, Montreal, QC H3T 1E2, Canada.
Department of Medicine, McGill University, Montreal, QC H3G 2M1, Canada.
Viruses. 2023 Mar 29;15(4):871. doi: 10.3390/v15040871.
The COVID-19 pandemic has resulted in upwards of 6.8 million deaths over the past three years, and the frequent emergence of variants continues to strain global health. Although vaccines have greatly helped mitigate disease severity, SARS-CoV-2 is likely to remain endemic, making it critical to understand its viral mechanisms contributing to pathogenesis and discover new antiviral therapeutics. To efficiently infect, this virus uses a diverse set of strategies to evade host immunity, accounting for its high pathogenicity and rapid spread throughout the COVID-19 pandemic. Behind some of these critical host evasion strategies is the accessory protein Open Reading Frame 8 (ORF8), which has gained recognition in SARS-CoV-2 pathogenesis due to its hypervariability, secretory property, and unique structure. This review discusses the current knowledge on SARS-CoV-2 ORF8 and proposes actualized functional models describing its pivotal roles in both viral replication and immune evasion. A better understanding of ORF8's interactions with host and viral factors is expected to reveal essential pathogenic strategies utilized by SARS-CoV-2 and inspire the development of novel therapeutics to improve COVID-19 disease outcomes.
在过去的三年中,COVID-19 大流行导致了超过 680 万人死亡,变种的频繁出现继续给全球健康带来压力。尽管疫苗极大地帮助减轻了疾病的严重程度,但 SARS-CoV-2 可能仍然会流行,因此了解其导致发病机制的病毒机制并发现新的抗病毒疗法至关重要。为了有效地感染,该病毒使用了多种策略来逃避宿主的免疫,这就是其高致病性和在整个 COVID-19 大流行期间迅速传播的原因。在这些关键的宿主逃逸策略背后的一些是辅助蛋白开放阅读框 8(ORF8),由于其高变异性、分泌特性和独特的结构,它在 SARS-CoV-2 发病机制中得到了认可。这篇综述讨论了目前关于 SARS-CoV-2 ORF8 的知识,并提出了实际的功能模型,描述了它在病毒复制和免疫逃逸中的关键作用。更好地了解 ORF8 与宿主和病毒因子的相互作用有望揭示 SARS-CoV-2 利用的重要发病策略,并激发新疗法的开发,以改善 COVID-19 的疾病结局。