Heterologous immunization with adenovirus vectored and inactivated vaccines effectively protects against SARS-CoV-2 variants in mice and macaques

To cope with the decline in COVID-19 vaccine-induced immunity caused by emerging SARS-CoV-2 variants, a heterologous immunization regimen using chimpanzee adenovirus vectored vaccine expressing SARS-CoV-2 spike (ChAd-S) and an inactivated vaccine (IV) was tested in mice and non-human primates (NHPs)...

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Veröffentlicht in:Frontiers in immunology 2022-08, Vol.13, p.949248-949248
Hauptverfasser: He, Qian, Mao, Qunying, Zhang, Jialu, Gao, Fan, Bai, Yu, Cui, Bopei, Liu, Jianyang, An, Chaoqiang, Wang, Qian, Yan, Xujia, Yang, Jinghuan, Song, Lifang, Song, Ziyang, Liu, Dong, Yuan, Yadi, Sun, Jing, Zhao, Jincun, Bian, Lianlian, Wu, Xing, Huang, Weijin, Li, Changgui, Wang, Junzhi, Liang, Zhenglun, Xu, Miao
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Sprache:eng
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Zusammenfassung:To cope with the decline in COVID-19 vaccine-induced immunity caused by emerging SARS-CoV-2 variants, a heterologous immunization regimen using chimpanzee adenovirus vectored vaccine expressing SARS-CoV-2 spike (ChAd-S) and an inactivated vaccine (IV) was tested in mice and non-human primates (NHPs). Heterologous regimen successfully enhanced or at least maintained antibody and T cell responses and effectively protected against SARS-CoV-2 variants in mice and NHPs. An additional heterologous booster in mice further improved and prolonged the spike-specific antibody response and conferred effective neutralizing activity against the Omicron variant. Interestingly, priming with ChAd-S and boosting with IV reduced the lung injury risk caused by T cell over activation in NHPs compared to homologous ChAd-S regimen, meanwhile maintained the flexibility of antibody regulation system to react to virus invasion by upregulating or preserving antibody levels. This study demonstrated the satisfactory compatibility of ChAd-S and IV in prime-boost vaccination in animal models.
ISSN:1664-3224
1664-3224
DOI:10.3389/fimmu.2022.949248