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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

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 immunobrid...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10026957/
https://www.ncbi.nlm.nih.gov/pubmed/36949953
http://dx.doi.org/10.3389/fimmu.2023.1106837
Descripción
Sumario: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.