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Waning immune responses against SARS-CoV-2 among vaccinees in Hong Kong
Qiaoli Peng; Runhong Zhou; Yuewen Wang; Meiqing Zhao; Na Liu; Shuang Li; Haode Huang; Dawei Yang; Ka-Kit Au; Kwan Man; Kwok-Yung Yuen; Zhiwei Chen.
Afiliação
  • Qiaoli Peng; The University of Hong Kong
  • Runhong Zhou; The University of Hong Kong
  • Yuewen Wang; The University of Hong Kong
  • Meiqing Zhao; The University of Hong Kong
  • Na Liu; The University of Hong Kong
  • Shuang Li; The University of Hong Kong
  • Haode Huang; The University of Hong Kong
  • Dawei Yang; The University of Hong Kong
  • Ka-Kit Au; The University of Hong Kong
  • Kwan Man; The University of Hong Kong
  • Kwok-Yung Yuen; The University of Hong Kong
  • Zhiwei Chen; The University of Hong Kong
Preprint em Inglês | bioRxiv | ID: ppbiorxiv-473934
ABSTRACT
BackgroundNearly 4 billion doses of the BioNTech-mRNA and Sinovac-inactivated vaccines have been administrated globally, yet different vaccine-induced immunity against SARS-CoV-2 variants of concern (VOCs) remain incompletely investigated. MethodsWe compare the immunogenicity and durability of these two vaccines among fully vaccinated Hong Kong people. FindingsStandard BioNTech and Sinovac vaccinations were tolerated and induced neutralizing antibody (NAb) (100% and 85.7%) and spike-specific CD4 T cell responses (96.7% and 82.1%), respectively. The geometric mean NAb IC50 and median frequencies of reactive CD4 subsets were consistently lower among Sinovac-vaccinees than BioNTech-vaccinees. Against VOCs, NAb response rate and geometric mean IC50 against B1.351 and B.1.617.2 were significantly lower for Sinovac (14.3%, 15 and 50%, 23.2) than BioNTech (79.4%, 107 and 94.1%, 131). Three months after vaccinations, NAbs to VOCs dropped near to detection limit, along with waning memory T cell responses, mainly among Sinovac-vaccinees. InterpretationOur results indicate that Sinovac-vaccinees may face higher risk to pandemic VOCs breakthrough infection. FundingThis study was supported by the Hong Kong Research Grants Council Collaborative Research Fund (C7156-20GF to Z.C and C1134-20GF); the National Program on Key Research Project of China (Grant 2020YFC0860600, 2020YFA0707500 and 2020YFA0707504); Shenzhen Science and Technology Program (JSGG20200225151410198 and JCYJ20210324131610027); HKU Development Fund and LKS Faculty of Medicine Matching Fund to AIDS Institute; Hong Kong Innovation and Technology Fund, Innovation and Technology Commission and generous donation from the Friends of Hope Education Fund. Z.C.s team was also partly supported by the Theme-Based Research Scheme (T11-706/18-N).
Licença
cc_by_nc_nd
Texto completo: Disponível Coleções: Preprints Base de dados: bioRxiv Tipo de estudo: Estudo prognóstico Idioma: Inglês Ano de publicação: 2021 Tipo de documento: Preprint
Texto completo: Disponível Coleções: Preprints Base de dados: bioRxiv Tipo de estudo: Estudo prognóstico Idioma: Inglês Ano de publicação: 2021 Tipo de documento: Preprint
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