Centre of Vaccinology, University of Geneva, Switzerland.
Independent Advisor, Stuart, FL, USA.
Vaccine. 2020 Jun 26;38(31):4783-4791. doi: 10.1016/j.vaccine.2020.05.064. Epub 2020 May 25.
A novel coronavirus (CoV), Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), emerged in late 2019 in Wuhan, China and has since spread as a global pandemic. Safe and effective vaccines are thus urgently needed to reduce the significant morbidity and mortality of Coronavirus Disease 2019 (COVID-19) disease and ease the major economic impact. There has been an unprecedented rapid response by vaccine developers with now over one hundred vaccine candidates in development and at least six having reached clinical trials. However, a major challenge during rapid development is to avoid safety issues both by thoughtful vaccine design and by thorough evaluation in a timely manner. A syndrome of "disease enhancement" has been reported in the past for a few viral vaccines where those immunized suffered increased severity or death when they later encountered the virus or were found to have an increased frequency of infection. Animal models allowed scientists to determine the underlying mechanism for the former in the case of Respiratory syncytial virus (RSV) vaccine and have been utilized to design and screen new RSV vaccine candidates. Because some Middle East respiratory syndrome (MERS) and SARS-CoV-1 vaccines have shown evidence of disease enhancement in some animal models, this is a particular concern for SARS-CoV-2 vaccines. To address this challenge, the Coalition for Epidemic Preparedness Innovations (CEPI) and the Brighton Collaboration (BC) Safety Platform for Emergency vACcines (SPEAC) convened a scientific working meeting on March 12 and 13, 2020 of experts in the field of vaccine immunology and coronaviruses to consider what vaccine designs could reduce safety concerns and how animal models and immunological assessments in early clinical trials can help to assess the risk. This report summarizes the evidence presented and provides considerations for safety assessment of COVID-19 vaccine candidates in accelerated vaccine development.
一种新型冠状病毒(CoV),即严重急性呼吸系统综合症冠状病毒 2 型(SARS-CoV-2),于 2019 年末在中国武汉出现,此后已在全球范围内蔓延,成为一种大流行疾病。因此,迫切需要安全有效的疫苗来降低冠状病毒病 2019(COVID-19)疾病的高发病率和死亡率,并缓解其对经济的重大影响。疫苗研发者已经做出了前所未有的快速响应,目前有超过一百种疫苗候选者正在研发中,至少有六种已经进入临床试验。然而,在快速开发过程中,一个主要挑战是既要通过深思熟虑的疫苗设计,又要及时进行全面评估,避免出现安全问题。过去曾有报道称,少数几种病毒疫苗出现了“疾病增强”综合征,即那些接种疫苗的人在后来遇到病毒或发现感染频率增加时,病情加重或死亡。动物模型使科学家能够确定呼吸道合胞病毒(RSV)疫苗的前一种情况的潜在机制,并已被用于设计和筛选新的 RSV 疫苗候选者。由于一些中东呼吸综合征(MERS)和 SARS-CoV-1 疫苗在一些动物模型中显示出疾病增强的证据,因此这是 SARS-CoV-2 疫苗特别关注的问题。为了应对这一挑战,传染病防范创新联盟(CEPI)和布莱顿合作组织(BC)紧急疫苗安全平台(SPEAC)于 2020 年 3 月 12 日至 13 日召集了疫苗免疫学和冠状病毒领域的专家举行了一次科学工作会议,讨论了哪些疫苗设计可以降低安全性问题,以及早期临床试验中的动物模型和免疫学评估如何帮助评估风险。本报告总结了提出的证据,并为加速疫苗开发中 COVID-19 疫苗候选者的安全性评估提供了考虑因素。