School of Chemistry and Molecular Biosciences, The University of Queensland, St. Lucia, QLD, 4072, Australia.
Institute for Molecular Bioscience, The University of Queensland, St. Lucia, QLD, 4072, Australia.
Adv Sci (Weinh). 2021 Aug;8(16):e2100985. doi: 10.1002/advs.202100985. Epub 2021 Jun 27.
COVID-19 is disastrous to global health and the economy. SARS-CoV-2 infection exhibits similar clinical symptoms and immunopathological sequelae to SARS-CoV infection. Therefore, much of the developmental progress on SARS-CoV vaccines can be utilized for the development of SARS-CoV-2 vaccines. Careful antigen selection during development is always of utmost importance for the production of effective vaccines that do not compromise recipient safety. This holds especially true for SARS-CoV vaccines, as several immunopathological disorders are associated with the activity of structural and nonstructural proteins encoded in the virus's genetic material. Whole viral protein and RNA-encoding full-length proteins contain both protective and "dangerous" sequences, unless pathological fragments are deleted. In light of recent advances, peptide vaccines may present a very safe and effective alternative. Peptide vaccines can avoid immunopathological pro-inflammatory sequences, focus immune responses on neutralizing immunogenic epitopes, avoid off-target antigen loss, combine antigens with different protective roles or mechanisms, even from different viral proteins, and avoid mutant escape by employing highly conserved cryptic epitopes. In this review, an attempt is made to exploit the similarities between SARS-CoV and SARS-CoV-2 in vaccine antigen screening, with particular attention to the pathological and immunogenic properties of SARS proteins.
COVID-19 对全球健康和经济造成了灾难性影响。SARS-CoV-2 感染表现出与 SARS-CoV 感染相似的临床症状和免疫病理后果。因此,SARS-CoV 疫苗的许多研发进展可用于 SARS-CoV-2 疫苗的开发。在开发过程中,仔细选择抗原对于生产不影响受体安全性的有效疫苗始终至关重要。对于 SARS-CoV 疫苗来说尤其如此,因为几种免疫病理疾病与病毒遗传物质编码的结构和非结构蛋白的活性有关。完整的病毒蛋白和 RNA 编码全长蛋白既包含保护性序列,也包含“危险”序列,除非删除病理片段。鉴于最近的进展,肽疫苗可能是一种非常安全有效的替代方法。肽疫苗可以避免免疫病理的促炎序列,将免疫反应集中在中和免疫原性表位上,避免非靶向抗原丢失,将具有不同保护作用或机制的抗原(甚至来自不同的病毒蛋白)结合起来,并通过使用高度保守的隐匿表位来避免突变逃逸。在这篇综述中,我们尝试利用 SARS-CoV 和 SARS-CoV-2 在疫苗抗原筛选中的相似性,特别关注 SARS 蛋白的病理和免疫原性特性。