Homologous and heterologous boosting of the Chadox1-S1-S COVID-19 vaccine with the SCB-2019 vaccine candidate : a randomized, controlled, phase 2 Study
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , , , , , , , , |
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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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 info:eu-repo/semantics/article |
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info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10183/255519 |
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2328-8957 |
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001159887 |
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http://hdl.handle.net/10183/255519 |
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eng |
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dc.relation.ispartof.pt_BR.fl_str_mv |
Open forum infectious diseases. Cary, NC. Vol. [9], no. [8 (Aug. 2022)], ofac418, 10 p. |
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