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Real-world effectiveness of homologous and heterologous BNT162b2, CoronaVac, and AZD1222 booster vaccination against Delta and Omicron SARS-CoV-2 infection

Given emerging evidence of immune escape in the SARS-CoV-2 Omicron viral variant, and its dominance, effectiveness of heterologous and homologous boosting schedules commonly used in low-to-middle income countries needs to be re-evaluated. We conducted a test-negative design using consolidated nation...

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Autores principales: Suah, Jing Lian, Tng, Boon Hwa, Tok, Peter Seah Keng, Husin, Masliyana, Thevananthan, Thevesh, Peariasamy, Kalaiarasu M., Sivasampu, Sheamini
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9132393/
https://www.ncbi.nlm.nih.gov/pubmed/35499301
http://dx.doi.org/10.1080/22221751.2022.2072773
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author Suah, Jing Lian
Tng, Boon Hwa
Tok, Peter Seah Keng
Husin, Masliyana
Thevananthan, Thevesh
Peariasamy, Kalaiarasu M.
Sivasampu, Sheamini
author_facet Suah, Jing Lian
Tng, Boon Hwa
Tok, Peter Seah Keng
Husin, Masliyana
Thevananthan, Thevesh
Peariasamy, Kalaiarasu M.
Sivasampu, Sheamini
author_sort Suah, Jing Lian
collection PubMed
description Given emerging evidence of immune escape in the SARS-CoV-2 Omicron viral variant, and its dominance, effectiveness of heterologous and homologous boosting schedules commonly used in low-to-middle income countries needs to be re-evaluated. We conducted a test-negative design using consolidated national administrative data in Malaysia to compare the effectiveness of homologous and heterologous BNT162b2, CoronaVac, and AZD1222 booster vaccination against SARS-CoV-2 infection in predominant-Delta and predominant-Omicron periods. Across both periods, homologous CoronaVac and AZD1222 boosting demonstrated lower effectiveness than heterologous boosting for CoronaVac and AZD1222 primary vaccination recipients and homologous BNT162b2 boosting. Broadly, marginal effectiveness was smaller by 40–50 percentage points in the Omicron period than the Delta period. Without effective and accessible second-generation vaccines, heterologous boosting using BNT162b2 for inactivated and vectored primary vaccination recipients is preferred.
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spelling pubmed-91323932022-05-26 Real-world effectiveness of homologous and heterologous BNT162b2, CoronaVac, and AZD1222 booster vaccination against Delta and Omicron SARS-CoV-2 infection Suah, Jing Lian Tng, Boon Hwa Tok, Peter Seah Keng Husin, Masliyana Thevananthan, Thevesh Peariasamy, Kalaiarasu M. Sivasampu, Sheamini Emerg Microbes Infect Coronaviruses Given emerging evidence of immune escape in the SARS-CoV-2 Omicron viral variant, and its dominance, effectiveness of heterologous and homologous boosting schedules commonly used in low-to-middle income countries needs to be re-evaluated. We conducted a test-negative design using consolidated national administrative data in Malaysia to compare the effectiveness of homologous and heterologous BNT162b2, CoronaVac, and AZD1222 booster vaccination against SARS-CoV-2 infection in predominant-Delta and predominant-Omicron periods. Across both periods, homologous CoronaVac and AZD1222 boosting demonstrated lower effectiveness than heterologous boosting for CoronaVac and AZD1222 primary vaccination recipients and homologous BNT162b2 boosting. Broadly, marginal effectiveness was smaller by 40–50 percentage points in the Omicron period than the Delta period. Without effective and accessible second-generation vaccines, heterologous boosting using BNT162b2 for inactivated and vectored primary vaccination recipients is preferred. Taylor & Francis 2022-05-23 /pmc/articles/PMC9132393/ /pubmed/35499301 http://dx.doi.org/10.1080/22221751.2022.2072773 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Coronaviruses
Suah, Jing Lian
Tng, Boon Hwa
Tok, Peter Seah Keng
Husin, Masliyana
Thevananthan, Thevesh
Peariasamy, Kalaiarasu M.
Sivasampu, Sheamini
Real-world effectiveness of homologous and heterologous BNT162b2, CoronaVac, and AZD1222 booster vaccination against Delta and Omicron SARS-CoV-2 infection
title Real-world effectiveness of homologous and heterologous BNT162b2, CoronaVac, and AZD1222 booster vaccination against Delta and Omicron SARS-CoV-2 infection
title_full Real-world effectiveness of homologous and heterologous BNT162b2, CoronaVac, and AZD1222 booster vaccination against Delta and Omicron SARS-CoV-2 infection
title_fullStr Real-world effectiveness of homologous and heterologous BNT162b2, CoronaVac, and AZD1222 booster vaccination against Delta and Omicron SARS-CoV-2 infection
title_full_unstemmed Real-world effectiveness of homologous and heterologous BNT162b2, CoronaVac, and AZD1222 booster vaccination against Delta and Omicron SARS-CoV-2 infection
title_short Real-world effectiveness of homologous and heterologous BNT162b2, CoronaVac, and AZD1222 booster vaccination against Delta and Omicron SARS-CoV-2 infection
title_sort real-world effectiveness of homologous and heterologous bnt162b2, coronavac, and azd1222 booster vaccination against delta and omicron sars-cov-2 infection
topic Coronaviruses
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9132393/
https://www.ncbi.nlm.nih.gov/pubmed/35499301
http://dx.doi.org/10.1080/22221751.2022.2072773
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