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Development of recombinant COVID-19 vaccine based on CHO-produced, prefusion spike trimer and alum/CpG adjuvants

COVID-19 pandemic has severely impacted the public health and social economy worldwide. A safe, effective, and affordable vaccine against SARS-CoV-2 infections/diseases is urgently needed. We have been developing a recombinant vaccine based on a prefusion-stabilized spike trimer of SARS-CoV-2 and fo...

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Detalles Bibliográficos
Autores principales: Liu, Haitao, Zhou, Chenliang, An, Jiao, Song, Yujiao, Yu, Pin, Li, Jiadai, Gu, Chenjian, Hu, Dongdong, Jiang, Yuanxiang, Zhang, Lingli, Huang, Chuanqi, Zhang, Chao, Yang, Yunqi, Zhu, Qianjun, Wang, Dekui, Liu, Yuqiang, Miao, Chenyang, Cao, Xiayao, Ding, Longfei, Zhu, Yuanfei, Zhu, Hua, Bao, Linlin, Zhou, Lingyun, Yan, Huan, Fan, Jiang, Xu, Jianqing, Hu, Zhongyu, Xie, Youhua, Liu, Jiangning, Liu, Ge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8556577/
https://www.ncbi.nlm.nih.gov/pubmed/34750014
http://dx.doi.org/10.1016/j.vaccine.2021.10.066
Descripción
Sumario:COVID-19 pandemic has severely impacted the public health and social economy worldwide. A safe, effective, and affordable vaccine against SARS-CoV-2 infections/diseases is urgently needed. We have been developing a recombinant vaccine based on a prefusion-stabilized spike trimer of SARS-CoV-2 and formulated with aluminium hydroxide and CpG 7909. The spike protein was expressed in Chinese hamster ovary (CHO) cells, purified, and prepared as a stable formulation with the dual adjuvant. Immunogenicity studies showed that candidate vaccines elicited robust neutralizing antibody responses and substantial CD4(+) T cell responses in both mice and non-human primates. And vaccine-induced neutralizing antibodies persisted at high level for at least 6 months. Challenge studies demonstrated that candidate vaccine reduced the viral loads and inflammation in the lungs of SARS-CoV-2 infected golden Syrian hamsters significantly. In addition, the vaccine-induced antibodies showed cross-neutralization activity against B.1.1.7 and B.1.351 variants. These data suggest candidate vaccine is efficacious in preventing SARS-CoV-2 infections and associated pneumonia, thereby justifying ongoing phase I/II clinical studies in China (NCT04982068 and NCT04990544).