Homologous and heterologous boosting of the Chadox1-S1-S COVID-19 vaccine with the SCB-2019 vaccine candidate : a randomized, controlled, phase 2 Study

Detalhes bibliográficos
Autor(a) principal: Clemens, Sue Ann Costa
Data de Publicação: 2022
Outros Autores: Milan, Eveline Pipolo, Sprinz, Eduardo, Cerbino Neto, José, Pacciarini, Filippo, Li, Ping, Chen, Hui-Ling, Smolenov, Igor V., Pollard, Andrew J., Clemens, Ralf
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/255519
Resumo: Background: Ongoing outbreaks of coronavirus disease 2019 (COVID-19) are driven by waning immunity following primary immunizations and emergence of new severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants that escape vaccineinduced neutralizing antibodies. It has been suggested that heterologous boosters could enhance and potentially maintain population immunity. Methods: We assessed the immunogenicity and reactogenicity of booster doses of different formulations of aluminium hydroxide–adjuvanted SCB-2019 vaccine (9 μg of SCB-2019, with or without CpG-1018 adjuvant, or 30 μg of SCB-2019 with CpG-1018) in Brazilian adults primed with ChAdOx1-S vector vaccine. S-protein antibodies and ACE2-binding inhibition were measured by enzyme-linked immunosorbent assay (ELISA) on days 1, 15, and 29. Participants self-reported solicited adverse events and reactions. Results: All SCB-2019 formulations increased S-protein ELISA antibodies and ACE2 binding inhibition to a greater extent than ChAdOx1-S. After 30 μg of SCB-2019 + CpG + aluminium hydroxide, titers against wild-type S-protein were significantly higher than after ChAdOx1-S on days 15 and 29, as were titers of neutralizing antibodies against the wild-type strain and Beta, Gamma, Delta, and Omicron variants. Boosting with SCB-2019 or ChAdOx1-S was well tolerated, with no vaccine-related serious or severe adverse events. Conclusions: Boosting ChAdOx1-S-primed adults with SCB-2019 induced higher levels of antibodies against a wild-type strain and SARS-CoV-2 variants than a homologous ChAdOx1-S booster, with the highest responses being with the 30-μg SCB-2019 + CpG + aluminium hydroxide formulation.
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spelling Clemens, Sue Ann CostaMilan, Eveline PipoloSprinz, EduardoCerbino Neto, JoséPacciarini, FilippoLi, PingChen, Hui-LingSmolenov, Igor V.Pollard, Andrew J.Clemens, Ralf2023-03-10T03:26:23Z20222328-8957http://hdl.handle.net/10183/255519001159887Background: Ongoing outbreaks of coronavirus disease 2019 (COVID-19) are driven by waning immunity following primary immunizations and emergence of new severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants that escape vaccineinduced neutralizing antibodies. It has been suggested that heterologous boosters could enhance and potentially maintain population immunity. Methods: We assessed the immunogenicity and reactogenicity of booster doses of different formulations of aluminium hydroxide–adjuvanted SCB-2019 vaccine (9 μg of SCB-2019, with or without CpG-1018 adjuvant, or 30 μg of SCB-2019 with CpG-1018) in Brazilian adults primed with ChAdOx1-S vector vaccine. S-protein antibodies and ACE2-binding inhibition were measured by enzyme-linked immunosorbent assay (ELISA) on days 1, 15, and 29. Participants self-reported solicited adverse events and reactions. Results: All SCB-2019 formulations increased S-protein ELISA antibodies and ACE2 binding inhibition to a greater extent than ChAdOx1-S. After 30 μg of SCB-2019 + CpG + aluminium hydroxide, titers against wild-type S-protein were significantly higher than after ChAdOx1-S on days 15 and 29, as were titers of neutralizing antibodies against the wild-type strain and Beta, Gamma, Delta, and Omicron variants. Boosting with SCB-2019 or ChAdOx1-S was well tolerated, with no vaccine-related serious or severe adverse events. Conclusions: Boosting ChAdOx1-S-primed adults with SCB-2019 induced higher levels of antibodies against a wild-type strain and SARS-CoV-2 variants than a homologous ChAdOx1-S booster, with the highest responses being with the 30-μg SCB-2019 + CpG + aluminium hydroxide formulation.application/pdfengOpen forum infectious diseases. Cary, NC. Vol. [9], no. [8 (Aug. 2022)], ofac418, 10 p.COVID-19Vacinas contra COVID-19Imunização secundáriaAntígenos heterófilosEnsaio clínico fase IISCB-2019BoosterChAdOx1-SHeterologousHomologousVaccineHomologous and heterologous boosting of the Chadox1-S1-S COVID-19 vaccine with the SCB-2019 vaccine candidate : a randomized, controlled, phase 2 StudyEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001159887.pdf.txt001159887.pdf.txtExtracted Texttext/plain39526http://www.lume.ufrgs.br/bitstream/10183/255519/2/001159887.pdf.txt691538f2a30cdc42b568015127c86af9MD52ORIGINAL001159887.pdfTexto completo (inglês)application/pdf826080http://www.lume.ufrgs.br/bitstream/10183/255519/1/001159887.pdfdc4982555142b2a0bff152318e3ff902MD5110183/2555192023-03-11 03:30:18.235329oai:www.lume.ufrgs.br:10183/255519Repositório InstitucionalPUBhttps://lume.ufrgs.br/oai/requestlume@ufrgs.bropendoar:2023-03-11T06:30:18Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Homologous and heterologous boosting of the Chadox1-S1-S COVID-19 vaccine with the SCB-2019 vaccine candidate : a randomized, controlled, phase 2 Study
title Homologous and heterologous boosting of the Chadox1-S1-S COVID-19 vaccine with the SCB-2019 vaccine candidate : a randomized, controlled, phase 2 Study
spellingShingle Homologous and heterologous boosting of the Chadox1-S1-S COVID-19 vaccine with the SCB-2019 vaccine candidate : a randomized, controlled, phase 2 Study
Clemens, Sue Ann Costa
COVID-19
Vacinas contra COVID-19
Imunização secundária
Antígenos heterófilos
Ensaio clínico fase II
SCB-2019
Booster
ChAdOx1-S
Heterologous
Homologous
Vaccine
title_short Homologous and heterologous boosting of the Chadox1-S1-S COVID-19 vaccine with the SCB-2019 vaccine candidate : a randomized, controlled, phase 2 Study
title_full Homologous and heterologous boosting of the Chadox1-S1-S COVID-19 vaccine with the SCB-2019 vaccine candidate : a randomized, controlled, phase 2 Study
title_fullStr Homologous and heterologous boosting of the Chadox1-S1-S COVID-19 vaccine with the SCB-2019 vaccine candidate : a randomized, controlled, phase 2 Study
title_full_unstemmed Homologous and heterologous boosting of the Chadox1-S1-S COVID-19 vaccine with the SCB-2019 vaccine candidate : a randomized, controlled, phase 2 Study
title_sort Homologous and heterologous boosting of the Chadox1-S1-S COVID-19 vaccine with the SCB-2019 vaccine candidate : a randomized, controlled, phase 2 Study
author Clemens, Sue Ann Costa
author_facet Clemens, Sue Ann Costa
Milan, Eveline Pipolo
Sprinz, Eduardo
Cerbino Neto, José
Pacciarini, Filippo
Li, Ping
Chen, Hui-Ling
Smolenov, Igor V.
Pollard, Andrew J.
Clemens, Ralf
author_role author
author2 Milan, Eveline Pipolo
Sprinz, Eduardo
Cerbino Neto, José
Pacciarini, Filippo
Li, Ping
Chen, Hui-Ling
Smolenov, Igor V.
Pollard, Andrew J.
Clemens, Ralf
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Clemens, Sue Ann Costa
Milan, Eveline Pipolo
Sprinz, Eduardo
Cerbino Neto, José
Pacciarini, Filippo
Li, Ping
Chen, Hui-Ling
Smolenov, Igor V.
Pollard, Andrew J.
Clemens, Ralf
dc.subject.por.fl_str_mv COVID-19
Vacinas contra COVID-19
Imunização secundária
Antígenos heterófilos
Ensaio clínico fase II
topic COVID-19
Vacinas contra COVID-19
Imunização secundária
Antígenos heterófilos
Ensaio clínico fase II
SCB-2019
Booster
ChAdOx1-S
Heterologous
Homologous
Vaccine
dc.subject.eng.fl_str_mv SCB-2019
Booster
ChAdOx1-S
Heterologous
Homologous
Vaccine
description Background: Ongoing outbreaks of coronavirus disease 2019 (COVID-19) are driven by waning immunity following primary immunizations and emergence of new severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants that escape vaccineinduced neutralizing antibodies. It has been suggested that heterologous boosters could enhance and potentially maintain population immunity. Methods: We assessed the immunogenicity and reactogenicity of booster doses of different formulations of aluminium hydroxide–adjuvanted SCB-2019 vaccine (9 μg of SCB-2019, with or without CpG-1018 adjuvant, or 30 μg of SCB-2019 with CpG-1018) in Brazilian adults primed with ChAdOx1-S vector vaccine. S-protein antibodies and ACE2-binding inhibition were measured by enzyme-linked immunosorbent assay (ELISA) on days 1, 15, and 29. Participants self-reported solicited adverse events and reactions. Results: All SCB-2019 formulations increased S-protein ELISA antibodies and ACE2 binding inhibition to a greater extent than ChAdOx1-S. After 30 μg of SCB-2019 + CpG + aluminium hydroxide, titers against wild-type S-protein were significantly higher than after ChAdOx1-S on days 15 and 29, as were titers of neutralizing antibodies against the wild-type strain and Beta, Gamma, Delta, and Omicron variants. Boosting with SCB-2019 or ChAdOx1-S was well tolerated, with no vaccine-related serious or severe adverse events. Conclusions: Boosting ChAdOx1-S-primed adults with SCB-2019 induced higher levels of antibodies against a wild-type strain and SARS-CoV-2 variants than a homologous ChAdOx1-S booster, with the highest responses being with the 30-μg SCB-2019 + CpG + aluminium hydroxide formulation.
publishDate 2022
dc.date.issued.fl_str_mv 2022
dc.date.accessioned.fl_str_mv 2023-03-10T03:26:23Z
dc.type.driver.fl_str_mv Estrangeiro
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dc.identifier.issn.pt_BR.fl_str_mv 2328-8957
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