Beth Israel Deaconess Medical Center, Center for Virology and Vaccine Research, Harvard Medical School, Boston, MA 02115, USA.
Viruses. 2022 Feb 12;14(2):380. doi: 10.3390/v14020380.
The persistent expansion of the coronavirus disease 2019 (COVID-19) global pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) requires the rapid development of safe and effective countermeasures to reduce transmission, morbidity, and mortality. Several highly efficacious vaccines are actively being deployed around the globe to expedite mass vaccination and control of COVID-19. Notably, viral vectored vaccines (VVVs) are among the first to be approved for global distribution and use. In this review, we examine the humoral, cellular, and innate immune responses elicited by viral vectors, and the immune correlates of protection against COVID-19 in preclinical and clinical studies. We also discuss the durability and breadth of immune response induced by VVVs and boosters. Finally, we present challenges associated with VVVs and offer solutions for overcoming certain limitations of current vaccine regimens. Collectively, this review provides the rationale for expanding the portfolio of VVVs against SARS-CoV-2.
由严重急性呼吸系统综合症冠状病毒 2 型(SARS-CoV-2)引起的 2019 年冠状病毒病(COVID-19)大流行持续蔓延,这需要迅速开发安全有效的对策来减少传播、发病率和死亡率。几种高效的疫苗正在全球范围内积极部署,以加快大规模疫苗接种和控制 COVID-19。值得注意的是,病毒载体疫苗(VVV)是首批获准在全球分发和使用的疫苗之一。在这篇综述中,我们研究了病毒载体引起的体液、细胞和先天免疫反应,以及临床前和临床研究中针对 COVID-19 的免疫保护相关性。我们还讨论了 VVVs 和加强针诱导的免疫反应的持久性和广度。最后,我们介绍了与 VVVs 相关的挑战,并提出了克服当前疫苗方案某些局限性的解决方案。总的来说,这篇综述为扩大 SARS-CoV-2 的 VVVs 组合提供了依据。