Zhao Fangxin, Zai Xiaodong, Zhang Zhiling, Xu Junjie, Chen Wei
Laboratory of Vaccine and Antibody Engineering, Beijing Institute of Biotechnology, Beijing, 10071, China.
School of Medicine, Zhejiang University, Hangzhou, 310058, China.
NPJ Vaccines. 2022 Dec 19;7(1):167. doi: 10.1038/s41541-022-00597-4.
The emergence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) had become a global concern because of its unexpectedly high pathogenicity and transmissibility. SARS-CoV-2 variants that reduce the immune protection elicited from previous vaccination or natural infection raise challenges in controlling the spread of the pandemic. The development of universal vaccines against these variants seems to be a practical solution to alleviate the physical and economic effects caused by this disease, but it is hard to achieve. In this review, we describe the high mutation rate of RNA viruses and dynamic molecular structures of SARS-CoV-2 variants in several major neutralizing epitopes, trying to answer the question of why universal vaccines are difficult to design. Understanding the biological basis of immune evasion is crucial for combating these obstacles. We then summarize several advancements worthy of further study, including heterologous prime-boost regimens, construction of chimeric immunogens, design of protein nanoparticle antigens, and utilization of conserved neutralizing epitopes. The fact that some immunogens can induce cross-reactive immune responses against heterologous coronaviruses provides hints for universal vaccine development. We hope this review can provide inspiration to current universal vaccine studies.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的出现因其出乎意料的高致病性和传播性而成为全球关注的问题。降低先前疫苗接种或自然感染所引发的免疫保护的SARS-CoV-2变体,给控制疫情传播带来了挑战。开发针对这些变体的通用疫苗似乎是减轻这种疾病所造成的身体和经济影响的切实可行的解决方案,但却很难实现。在这篇综述中,我们描述了RNA病毒的高突变率以及SARS-CoV-2变体在几个主要中和表位中的动态分子结构,试图回答为什么通用疫苗难以设计的问题。了解免疫逃逸的生物学基础对于克服这些障碍至关重要。然后,我们总结了几项值得进一步研究的进展,包括异源初免-加强方案、嵌合免疫原的构建、蛋白质纳米颗粒抗原的设计以及保守中和表位的利用。一些免疫原能够诱导针对异源冠状病毒的交叉反应性免疫应答这一事实,为通用疫苗的开发提供了线索。我们希望这篇综述能够为当前的通用疫苗研究提供启发。