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Article: Immunogenicity against wild-type and Omicron SARS-CoV-2 after a third dose of inactivated COVID-19 vaccine in healthy adolescents

TitleImmunogenicity against wild-type and Omicron SARS-CoV-2 after a third dose of inactivated COVID-19 vaccine in healthy adolescents
Authors
Keywordsadolescent
CoronaVac
COVID-19
Omicron
vaccine
Issue Date2023
Citation
Frontiers in Immunology, 2023, v. 14, article no. 1106837 How to Cite?
AbstractIntroduction: 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.
Persistent Identifierhttp://hdl.handle.net/10722/343415
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLeung, Daniel-
dc.contributor.authorCohen, Carolyn A.-
dc.contributor.authorMu, Xiaofeng-
dc.contributor.authorRosa Duque, Jaime S.-
dc.contributor.authorCheng, Samuel M.S.-
dc.contributor.authorWang, Xiwei-
dc.contributor.authorWang, Manni-
dc.contributor.authorZhang, Wenyue-
dc.contributor.authorZhang, Yanmei-
dc.contributor.authorTam, Issan Y.S.-
dc.contributor.authorLam, Jennifer H.Y.-
dc.contributor.authorChan, Sau Man-
dc.contributor.authorChaothai, Sara-
dc.contributor.authorKwan, Kelvin K.H.-
dc.contributor.authorChan, Karl C.K.-
dc.contributor.authorLi, John K.C.-
dc.contributor.authorLuk, Leo L.H.-
dc.contributor.authorTsang, Leo C.H.-
dc.contributor.authorChu, Nym Coco-
dc.contributor.authorWong, Wilfred H.S.-
dc.contributor.authorMori, Masashi-
dc.contributor.authorLeung, Wing Hang-
dc.contributor.authorValkenburg, Sophie-
dc.contributor.authorPeiris, Malik-
dc.contributor.authorTu, Wenwei-
dc.contributor.authorLau, Yu Lung-
dc.date.accessioned2024-05-10T09:07:57Z-
dc.date.available2024-05-10T09:07:57Z-
dc.date.issued2023-
dc.identifier.citationFrontiers in Immunology, 2023, v. 14, article no. 1106837-
dc.identifier.urihttp://hdl.handle.net/10722/343415-
dc.description.abstractIntroduction: 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.-
dc.languageeng-
dc.relation.ispartofFrontiers in Immunology-
dc.subjectadolescent-
dc.subjectCoronaVac-
dc.subjectCOVID-19-
dc.subjectOmicron-
dc.subjectvaccine-
dc.titleImmunogenicity against wild-type and Omicron SARS-CoV-2 after a third dose of inactivated COVID-19 vaccine in healthy adolescents-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.3389/fimmu.2023.1106837-
dc.identifier.pmid36949953-
dc.identifier.scopuseid_2-s2.0-85150492068-
dc.identifier.volume14-
dc.identifier.spagearticle no. 1106837-
dc.identifier.epagearticle no. 1106837-
dc.identifier.eissn1664-3224-
dc.identifier.isiWOS:000953268200001-

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