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Immunogenicity against wild-type and Omicron SARS-CoV-2 after a third dose of inactivated COVID-19 vaccine in healthy adolescents.
Leung, Daniel; Cohen, Carolyn A; Mu, Xiaofeng; Rosa Duque, Jaime S; Cheng, Samuel M S; Wang, Xiwei; Wang, Manni; Zhang, Wenyue; Zhang, Yanmei; Tam, Issan Y S; Lam, Jennifer H Y; Chan, Sau Man; Chaothai, Sara; Kwan, Kelvin K H; Chan, Karl C K; Li, John K C; Luk, Leo L H; Tsang, Leo C H; Chu, Nym Coco; Wong, Wilfred H S; Mori, Masashi; Leung, Wing Hang; Valkenburg, Sophie; Peiris, Malik; Tu, Wenwei; Lau, Yu Lung.
Affiliation
  • Leung D; Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong, Hong Kong SAR, China.
  • Cohen CA; School of Public Health, The University of Hong Kong, Hong Kong, Hong Kong SAR, China.
  • Mu X; HKU-Pasteur Research Pole, School of Public Health, The University of Hong Kong, Hong Kong, Hong Kong SAR, China.
  • Rosa Duque JS; Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong, Hong Kong SAR, China.
  • Cheng SMS; Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong, Hong Kong SAR, China.
  • Wang X; School of Public Health, The University of Hong Kong, Hong Kong, Hong Kong SAR, China.
  • Wang M; Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong, Hong Kong SAR, China.
  • Zhang W; Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong, Hong Kong SAR, China.
  • Zhang Y; Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong, Hong Kong SAR, China.
  • Tam IYS; Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong, Hong Kong SAR, China.
  • Lam JHY; Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong, Hong Kong SAR, China.
  • Chan SM; Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong, Hong Kong SAR, China.
  • Chaothai S; Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong, Hong Kong SAR, China.
  • Kwan KKH; School of Public Health, The University of Hong Kong, Hong Kong, Hong Kong SAR, China.
  • Chan KCK; School of Public Health, The University of Hong Kong, Hong Kong, Hong Kong SAR, China.
  • Li JKC; School of Public Health, The University of Hong Kong, Hong Kong, Hong Kong SAR, China.
  • Luk LLH; School of Public Health, The University of Hong Kong, Hong Kong, Hong Kong SAR, China.
  • Tsang LCH; School of Public Health, The University of Hong Kong, Hong Kong, Hong Kong SAR, China.
  • Chu NC; School of Public Health, The University of Hong Kong, Hong Kong, Hong Kong SAR, China.
  • Wong WHS; School of Public Health, The University of Hong Kong, Hong Kong, Hong Kong SAR, China.
  • Mori M; Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong, Hong Kong SAR, China.
  • Leung WH; Research Institute for Bioresources and Biotechnology, Ishikawa Prefectural University, Nonoichi, Japan.
  • Valkenburg S; Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong, Hong Kong SAR, China.
  • Peiris M; School of Public Health, The University of Hong Kong, Hong Kong, Hong Kong SAR, China.
  • Tu W; HKU-Pasteur Research Pole, School of Public Health, The University of Hong Kong, Hong Kong, Hong Kong SAR, China.
  • Lau YL; Department of Microbiology and Immunology, Peter Doherty Institute for Infection and Immunity, University of Melbourne, Melbourne, VIC, Australia.
Front Immunol ; 14: 1106837, 2023.
Article in En | MEDLINE | ID: mdl-36949953
Introduction: Two doses of inactivated SARS-CoV-2 vaccine CoronaVac cannot elicit high efficacy against symptomatic COVID-19, especially against the Omicron variant, but that can be improved by a third dose in adults. The use of a third dose of CoronaVac in adolescents may be supported by immunobridging studies in the absence of efficacy data. Methods: With an immunobridging design, our study (NCT04800133) tested the non-inferiority of the binding and neutralizing antibodies and T cell responses induced by a third dose of CoronaVac in healthy adolescents (N=94, median age 14.2 years, 56% male) compared to adults (N=153, median age 48.1 years, 44% male). Responses against wild-type (WT) and BA.1 SARS-CoV-2 were compared in adolescents. Safety and reactogenicity were also monitored. Results: A homologous third dose of CoronaVac further enhanced antibody response in adolescents compared to just 2 doses. Adolescents mounted non-inferior antibody and T cell responses compared to adults. Although S IgG and neutralizing antibody responses to BA.1 were lower than to WT, they remained detectable in 96% and 86% of adolescents. T cell responses to peptide pools spanning only the mutations of BA.1 S, N and M in adolescents were preserved, increased, and halved compared to WT respectively. No safety concerns were identified. Discussion: The primary vaccination series of inactivated SARS-CoV-2 vaccines for adolescents should include 3 doses for improved humoral immunogenicity.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: COVID-19 Vaccines / COVID-19 Limits: Adolescent / Adult / Female / Humans / Male / Middle aged Language: En Journal: Front Immunol Year: 2023 Document type: Article Affiliation country: China Country of publication: Suiza

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: COVID-19 Vaccines / COVID-19 Limits: Adolescent / Adult / Female / Humans / Male / Middle aged Language: En Journal: Front Immunol Year: 2023 Document type: Article Affiliation country: China Country of publication: Suiza