Department of Infectious Disease, St Mary's Campus, Imperial College London, London, UK.
Clin Exp Immunol. 2020 Nov;202(2):162-192. doi: 10.1111/cei.13517. Epub 2020 Oct 18.
Since the emergence of COVID-19, caused by the SARS-CoV-2 virus at the end of 2019, there has been an explosion of vaccine development. By 24 September 2020, a staggering number of vaccines (more than 200) had started preclinical development, of which 43 had entered clinical trials, including some approaches that have not previously been licensed for human vaccines. Vaccines have been widely considered as part of the exit strategy to enable the return to previous patterns of working, schooling and socializing. Importantly, to effectively control the COVID-19 pandemic, production needs to be scaled-up from a small number of preclinical doses to enough filled vials to immunize the world's population, which requires close engagement with manufacturers and regulators. It will require a global effort to control the virus, necessitating equitable access for all countries to effective vaccines. This review explores the immune responses required to protect against SARS-CoV-2 and the potential for vaccine-induced immunopathology. We describe the profile of the different platforms and the advantages and disadvantages of each approach. The review also addresses the critical steps between promising preclinical leads and manufacturing at scale. The issues faced during this pandemic and the platforms being developed to address it will be invaluable for future outbreak control. Nine months after the outbreak began we are at a point where preclinical and early clinical data are being generated for the vaccines; an overview of this important area will help our understanding of the next phases.
自 2019 年底由 SARS-CoV-2 病毒引起的 COVID-19 出现以来,疫苗的研发如雨后春笋般涌现。截至 2020 年 9 月 24 日,已有令人震惊的 200 多种疫苗开始进行临床前开发,其中 43 种已进入临床试验,包括一些以前未获准用于人类疫苗的方法。疫苗被广泛认为是恢复到以前的工作、学习和社交模式的退出策略的一部分。重要的是,为了有效控制 COVID-19 大流行,需要将生产从少数临床前剂量扩大到足以装满小瓶以免疫世界人口,这需要与制造商和监管机构密切合作。控制病毒需要全球共同努力,所有国家都需要公平获得有效的疫苗。本综述探讨了预防 SARS-CoV-2 所需的免疫反应以及疫苗引起的免疫病理的可能性。我们描述了不同平台的概况以及每种方法的优缺点。该综述还解决了从有希望的临床前先导到大规模生产的关键步骤。在大流行期间面临的问题以及为解决这些问题而开发的平台对于未来的疫情控制将是非常宝贵的。疫情爆发九个月后,我们已经获得了疫苗的临床前和早期临床数据;对这一重要领域的概述将有助于我们理解下一阶段。