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Safety and immunogenicity of heterologous COVID-19 vaccine regimens to deal with product shortage: A randomised clinical trial in an elderly population
OBJECTIVES: In a context of COVID-19 vaccine shortages, this study sought to evaluate the safety and efficacy of receiving one dose of Gam-COVID-Vac rAd26 followed by a second COVID-19 vaccine dose of either Gam-COVID-Vac rAd5, ChAdOx1 nCoV-19 or BBIBP-CorV in a cohort of older adults. STUDY DESIGN:...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9444309/ https://www.ncbi.nlm.nih.gov/pubmed/36090797 http://dx.doi.org/10.1016/j.puhip.2022.100313 |
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author | Kundro, M.A. Losso, M.H. Macchia, A. Pastor, I. Alonso Serena, M. Gestoso, C. Moreno Macías, L. Crupi, F. Acosta, M.C. Ivalo, S. Ghioldi, M. Bouzas, M.B. Mammana, L. Zapiola, I. Mazzitelli, I. Varese, A. Geffner, J. Biscayart, C. Angeleri, P. Lopez, E. Gentile, A. Ferrante, D. de Quiros, F. Gonzalez B. |
author_facet | Kundro, M.A. Losso, M.H. Macchia, A. Pastor, I. Alonso Serena, M. Gestoso, C. Moreno Macías, L. Crupi, F. Acosta, M.C. Ivalo, S. Ghioldi, M. Bouzas, M.B. Mammana, L. Zapiola, I. Mazzitelli, I. Varese, A. Geffner, J. Biscayart, C. Angeleri, P. Lopez, E. Gentile, A. Ferrante, D. de Quiros, F. Gonzalez B. |
author_sort | Kundro, M.A. |
collection | PubMed |
description | OBJECTIVES: In a context of COVID-19 vaccine shortages, this study sought to evaluate the safety and efficacy of receiving one dose of Gam-COVID-Vac rAd26 followed by a second COVID-19 vaccine dose of either Gam-COVID-Vac rAd5, ChAdOx1 nCoV-19 or BBIBP-CorV in a cohort of older adults. STUDY DESIGN: Single-centre, randomised, open label, non-inferiority trial. METHODS: Adults aged ≥65 years who had received one dose of Gam-COVID-Vac rAd26 were randomised in a 1:1:1 ratio to receive a second-dose COVID-19 vaccination of either Gam-COVID-Vac rAd5, ChAdOx1 nCoV-19 or BBIBP-CorV. The primary outcome was the assessment of the humoral immune response to vaccination (i.e. antibody titres of SARS-CoV-2 spike protein at 28 days after second-dose vaccination). In addition, neutralising antibody titres at day 28 for the three schedules were measured. RESULTS: Of 85 participants who were enrolled in the study between 26 and July 30, 2021, 31 individuals were randomised to receive Gam-COVID-Vac rAd5, 27 to ChAdOx1 nCoV-19 and 27 to BBIBP-CorV. The mean age of participants was 68.2 years (SD 2.9) and 49 (57.6%) were female. Participants who received Gam-COVID-Vac rAd5 and ChAdOx1 nCoV1-19 showed significantly increased anti-S titres at 28 days after second-dose vaccination, but this magnitude of difference was not observed for those who received BBIBP-CorV. The ratio between the geometric mean at day 28 and baseline within each group was 11.8 (6.98–19.89) among patients assigned to Gam-COVID-Vac rAd26/rAd5, 4.81 (2.14–10.81) for the rAd26/ChAdOx1 nCoV-19 group and 1.53 (0.74–3.20) for the rAd26/BBIBP-CorV group. All of the schedules were shown to be safe. CONCLUSIONS: The findings in this study contribute to the scarce information published on the safety and immunogenicity of Gam-COVID-Vac heterologous regimens and will help the development of guidelines and vaccine programme management. |
format | Online Article Text |
id | pubmed-9444309 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-94443092022-09-06 Safety and immunogenicity of heterologous COVID-19 vaccine regimens to deal with product shortage: A randomised clinical trial in an elderly population Kundro, M.A. Losso, M.H. Macchia, A. Pastor, I. Alonso Serena, M. Gestoso, C. Moreno Macías, L. Crupi, F. Acosta, M.C. Ivalo, S. Ghioldi, M. Bouzas, M.B. Mammana, L. Zapiola, I. Mazzitelli, I. Varese, A. Geffner, J. Biscayart, C. Angeleri, P. Lopez, E. Gentile, A. Ferrante, D. de Quiros, F. Gonzalez B. Public Health Pract (Oxf) Original Research OBJECTIVES: In a context of COVID-19 vaccine shortages, this study sought to evaluate the safety and efficacy of receiving one dose of Gam-COVID-Vac rAd26 followed by a second COVID-19 vaccine dose of either Gam-COVID-Vac rAd5, ChAdOx1 nCoV-19 or BBIBP-CorV in a cohort of older adults. STUDY DESIGN: Single-centre, randomised, open label, non-inferiority trial. METHODS: Adults aged ≥65 years who had received one dose of Gam-COVID-Vac rAd26 were randomised in a 1:1:1 ratio to receive a second-dose COVID-19 vaccination of either Gam-COVID-Vac rAd5, ChAdOx1 nCoV-19 or BBIBP-CorV. The primary outcome was the assessment of the humoral immune response to vaccination (i.e. antibody titres of SARS-CoV-2 spike protein at 28 days after second-dose vaccination). In addition, neutralising antibody titres at day 28 for the three schedules were measured. RESULTS: Of 85 participants who were enrolled in the study between 26 and July 30, 2021, 31 individuals were randomised to receive Gam-COVID-Vac rAd5, 27 to ChAdOx1 nCoV-19 and 27 to BBIBP-CorV. The mean age of participants was 68.2 years (SD 2.9) and 49 (57.6%) were female. Participants who received Gam-COVID-Vac rAd5 and ChAdOx1 nCoV1-19 showed significantly increased anti-S titres at 28 days after second-dose vaccination, but this magnitude of difference was not observed for those who received BBIBP-CorV. The ratio between the geometric mean at day 28 and baseline within each group was 11.8 (6.98–19.89) among patients assigned to Gam-COVID-Vac rAd26/rAd5, 4.81 (2.14–10.81) for the rAd26/ChAdOx1 nCoV-19 group and 1.53 (0.74–3.20) for the rAd26/BBIBP-CorV group. All of the schedules were shown to be safe. CONCLUSIONS: The findings in this study contribute to the scarce information published on the safety and immunogenicity of Gam-COVID-Vac heterologous regimens and will help the development of guidelines and vaccine programme management. Elsevier 2022-09-06 /pmc/articles/PMC9444309/ /pubmed/36090797 http://dx.doi.org/10.1016/j.puhip.2022.100313 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Research Kundro, M.A. Losso, M.H. Macchia, A. Pastor, I. Alonso Serena, M. Gestoso, C. Moreno Macías, L. Crupi, F. Acosta, M.C. Ivalo, S. Ghioldi, M. Bouzas, M.B. Mammana, L. Zapiola, I. Mazzitelli, I. Varese, A. Geffner, J. Biscayart, C. Angeleri, P. Lopez, E. Gentile, A. Ferrante, D. de Quiros, F. Gonzalez B. Safety and immunogenicity of heterologous COVID-19 vaccine regimens to deal with product shortage: A randomised clinical trial in an elderly population |
title | Safety and immunogenicity of heterologous COVID-19 vaccine regimens to deal with product shortage: A randomised clinical trial in an elderly population |
title_full | Safety and immunogenicity of heterologous COVID-19 vaccine regimens to deal with product shortage: A randomised clinical trial in an elderly population |
title_fullStr | Safety and immunogenicity of heterologous COVID-19 vaccine regimens to deal with product shortage: A randomised clinical trial in an elderly population |
title_full_unstemmed | Safety and immunogenicity of heterologous COVID-19 vaccine regimens to deal with product shortage: A randomised clinical trial in an elderly population |
title_short | Safety and immunogenicity of heterologous COVID-19 vaccine regimens to deal with product shortage: A randomised clinical trial in an elderly population |
title_sort | safety and immunogenicity of heterologous covid-19 vaccine regimens to deal with product shortage: a randomised clinical trial in an elderly population |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9444309/ https://www.ncbi.nlm.nih.gov/pubmed/36090797 http://dx.doi.org/10.1016/j.puhip.2022.100313 |
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