Study of efficacy and antibody duration to fourth-dose booster of Ad5-nCoV or inactivated SARS-CoV-2 vaccine in Chinese adults: a prospective cohort study

Introduction China experienced a record surge of coronavirus disease 2019 cases in December 2022, during the pandemic. Methods We conducted a randomized, parallel-controlled prospective cohort study to evaluate efficacy and antibody duration after a fourth-dose booster with Ad5-nCoV or inactivated s...

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Published inFrontiers in immunology Vol. 14; p. 1244373
Main Authors Xu, Nani, Xu, Yu, Dai, Rongrong, Zheng, Lin, Qin, Pan, Wan, Peng, Yang, Yejing, Jiang, Jianmin, Zhang, Hangjie, Hu, Xiaowei, Lv, Huakun
Format Journal Article
LanguageEnglish
Published Frontiers Media S.A 06.09.2023
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Summary:Introduction China experienced a record surge of coronavirus disease 2019 cases in December 2022, during the pandemic. Methods We conducted a randomized, parallel-controlled prospective cohort study to evaluate efficacy and antibody duration after a fourth-dose booster with Ad5-nCoV or inactivated severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine. Results A total of 191 participants aged ≥18 years who had completed a three-dose regimen of the inactivated SARS-CoV-2 vaccine 6 months earlier were recruited to receive the intramuscular Ad5-nCoV booster or the inactivated SARS-CoV-2 vaccine. The Ad5-nCoV group had significantly higher antibody levels compared with the inactivated vaccine group at 6 months after the fourth vaccination dose. After the pandemic, the breakthrough infection rate for the Ad5-nCoV and the inactivated vaccine groups was 77.89% and 78.13%, respectively. Survival curve analysis ( p = 0.872) and multivariable logistic regression analysis ( p = 0.956) showed no statistically significant differences in breakthrough infection between the two groups. Discussion Compared with a homologous fourth dose, a heterologous fourth dose of Ad5-nCoV elicited a higher immunogenic response in healthy adults who had been immunized with three doses of inactivated vaccine. Nevertheless, the efficacy of the two vaccine types was equivalent after the pandemic.
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Reviewed by: Larry Ellingsworth, Novavax, Inc., United States; Weina Sun, Icahn School of Medicine at Mount Sinai, United States
These authors have contributed equally to this work and share first authorship
Edited by: Mrinmoy Sanyal, Stanford University, United States
ISSN:1664-3224
1664-3224
DOI:10.3389/fimmu.2023.1244373