Center for Virology and Vaccine Research, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215, USA; email:
Harvard Medical School, Boston, Massachusetts 02115, USA.
Annu Rev Med. 2022 Jan 27;73:41-54. doi: 10.1146/annurev-med-012621-102252. Epub 2021 Oct 5.
The worldwide pandemic of coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has led to the unprecedented pace of development of multiple vaccines. This review evaluates how adenovirus (Ad) vector platforms have been leveraged in response to this pandemic. Ad vectors have been used in the past for vaccines against other viruses, most notably HIV and Ebola, but they never have been produced, distributed, or administered to humans at such a large scale. Several different serotypes of Ads encoding SARS-CoV-2 Spike have been tested and found to be efficacious against COVID-19. As vaccine rollouts continue and the number of people receiving these vaccines increases, we will continue to learn about this vaccine platform for COVID-19 prevention and control.
由严重急性呼吸系统综合征冠状病毒 2 型(SARS-CoV-2)引起的 2019 年冠状病毒病(COVID-19)全球大流行,导致多种疫苗以前所未有的速度发展。这篇综述评估了腺病毒(Ad)载体平台如何应对这一大流行。腺病毒载体过去曾被用于针对其他病毒(尤其是 HIV 和埃博拉病毒)的疫苗,但从未以如此大规模的方式在人类中生产、分发或使用。已经测试了几种编码 SARS-CoV-2 刺突蛋白的不同血清型 Ad,发现它们对 COVID-19 有效。随着疫苗的推出和接种这些疫苗的人数不断增加,我们将继续了解这种用于 COVID-19 预防和控制的疫苗平台。
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