Cell research · 2022
A variant-proof SARS-CoV-2 vaccine targeting HR1 domain in S2 subunit of spike protein.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
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Pang Wei, Lu Ying, Zhao Yan-Bo, Shen Fan, Fan Chang-Fa, Wang Qian, He Wen-Qiang, He Xiao-Yan, Li Ze-Kai, Chen Tao-Tao, Yang Cui-Xian, Li You-Zhi, Xiao Si-Xuan, Zhao Zu-Jiang, Huang Xu-Sheng, Luo Rong-Hua, Yang Liu-Meng, Zhang Mi, Dong Xing-Qi, Li Ming-Hua, Feng Xiao-Li, Zhou Qing-Cui, Qu Wang, Jiang Shibo, Ouyang Songying, Zheng Yong-Tang
Аннотация
The emerging SARS-CoV-2 variants, commonly with many mutations in S1 subunit of spike (S) protein are weakening the efficacy of the current vaccines and antibody therapeutics. This calls for the variant-proof SARS-CoV-2 vaccines targeting the more conserved regions in S protein. Here, we designed a recombinant subunit vaccine, HR121, targeting the conserved HR1 domain in S2 subunit of S protein. HR121 consisting of HR1-linker1-HR2-linker2-HR1, is conformationally and functionally analogous to the HR1 domain present in the fusion intermediate conformation of S2 subunit. Immunization with HR121 in rabbits and rhesus macaques elicited highly potent cross-neutralizing antibodies against SARS-CoV-2 and its variants, particularly Omicron sublineages. Vaccination with HR121 achieved near-full protections against prototype SARS-CoV-2 infection in hACE2 transgenic mice, Syrian golden hamsters and rhesus macaques, and effective protection against Omicron BA.2 infection in Syrian golden hamsters. This study demonstrates that HR121 is a promising candidate of variant-proof SARS-CoV-2 vaccine with a novel conserved target in the S2 subunit for application against current and future SARS-CoV-2 variants.