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Plaque-neutralizing antibody to BA.2.12.1, BA.4 and BA.5 in individuals with three doses of BioNTech or CoronaVac vaccines, natural infection and breakthrough infection

BACKGROUND: BA.2.12.1, BA.4 and BA.5 subvariants of SARS-CoV-2 variant-of-concern (VOC) Omicron (B.1.1.529) are spreading globally. They demonstrate higher transmissibility and immune escape. OBJECTIVES: Determine BA.2.12.1, BA.4 and BA.5 virus plaque reduction neutralization test (PRNT) antibody ti...

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Autores principales: Cheng, Samuel SM, Mok, Chris KP, Li, John KC, Ng, Susanna S, Lam, Bosco HS, Jeevan, Trushar, Kandeil, Ahmed, Pekosz, Andrew, Chan, Karl CK, Tsang, Leo CH, Ko, Fanny W, Chen, Chunke, Yiu, Karen, Luk, Leo LH, Chan, Ken KP, Webby, Richard J, Poon, Leo LM, Hui, David SC, Peiris, Malik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Authors. Published by Elsevier B.V. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9428331/
https://www.ncbi.nlm.nih.gov/pubmed/36081282
http://dx.doi.org/10.1016/j.jcv.2022.105273
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author Cheng, Samuel SM
Mok, Chris KP
Li, John KC
Ng, Susanna S
Lam, Bosco HS
Jeevan, Trushar
Kandeil, Ahmed
Pekosz, Andrew
Chan, Karl CK
Tsang, Leo CH
Ko, Fanny W
Chen, Chunke
Yiu, Karen
Luk, Leo LH
Chan, Ken KP
Webby, Richard J
Poon, Leo LM
Hui, David SC
Peiris, Malik
author_facet Cheng, Samuel SM
Mok, Chris KP
Li, John KC
Ng, Susanna S
Lam, Bosco HS
Jeevan, Trushar
Kandeil, Ahmed
Pekosz, Andrew
Chan, Karl CK
Tsang, Leo CH
Ko, Fanny W
Chen, Chunke
Yiu, Karen
Luk, Leo LH
Chan, Ken KP
Webby, Richard J
Poon, Leo LM
Hui, David SC
Peiris, Malik
author_sort Cheng, Samuel SM
collection PubMed
description BACKGROUND: BA.2.12.1, BA.4 and BA.5 subvariants of SARS-CoV-2 variant-of-concern (VOC) Omicron (B.1.1.529) are spreading globally. They demonstrate higher transmissibility and immune escape. OBJECTIVES: Determine BA.2.12.1, BA.4 and BA.5 virus plaque reduction neutralization test (PRNT) antibody titres in individuals recently vaccinated with BNT162b2 (n = 20) or CoronaVac (n = 20) vaccines or those convalescent from ancestral wild- type (WT) SARS-CoV-2 (n = 20) or BA.2 infections with (n = 17) or without (n = 7) prior vaccination. RESULTS: Relative to neutralization of the WT virus, those vaccinated with BNT162b2 had 4.8, 3.4, 4.6, 11.3 and 15.5-fold reductions of geometric mean antibody titres (GMT) to BA.1, BA.2, BA.2.12.1, BA.4 and BA.5 viruses, respectively. Similarly, those vaccinated with CoronaVac had 8.0, 7.0, 11.8, 12.0 and 12.0 fold GMT reductions and those with two doses of CoronaVac boosted by BNT162b2 had 6.1, 6.7, 6,3, 13.0 and 21.2 fold GMT reductions to these viruses, respectively. Vaccinated individuals with BA.2 breakthrough infections had higher GMT antibody levels vs. BA.4 (36.9) and BA.5 (36.9) than unvaccinated individuals with BA.2 infections (BA.4 GMT 8.2; BA.5 GMT 11.0). CONCLUSIONS: BA.4 and BA.5 subvariants were less susceptible to BNT162b2 or CoronaVac vaccine elicited antibody neutralization than subvariants BA.1, BA.2 and BA.2.12.1. Nevertheless, three doses BNT162b2 or booster of BNT162b2 following two doses of CoronaVac elicited detectable BA.4 and BA.5 neutralizing antibody responses while those vaccinated with three doses of CoronaVac largely fail to do so. BA.2 infections in vaccinated individuals led to higher levels of BA.4 or BA.5 neutralizing antibody compared to those who were vaccine-naive.
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spelling pubmed-94283312022-08-31 Plaque-neutralizing antibody to BA.2.12.1, BA.4 and BA.5 in individuals with three doses of BioNTech or CoronaVac vaccines, natural infection and breakthrough infection Cheng, Samuel SM Mok, Chris KP Li, John KC Ng, Susanna S Lam, Bosco HS Jeevan, Trushar Kandeil, Ahmed Pekosz, Andrew Chan, Karl CK Tsang, Leo CH Ko, Fanny W Chen, Chunke Yiu, Karen Luk, Leo LH Chan, Ken KP Webby, Richard J Poon, Leo LM Hui, David SC Peiris, Malik J Clin Virol Article BACKGROUND: BA.2.12.1, BA.4 and BA.5 subvariants of SARS-CoV-2 variant-of-concern (VOC) Omicron (B.1.1.529) are spreading globally. They demonstrate higher transmissibility and immune escape. OBJECTIVES: Determine BA.2.12.1, BA.4 and BA.5 virus plaque reduction neutralization test (PRNT) antibody titres in individuals recently vaccinated with BNT162b2 (n = 20) or CoronaVac (n = 20) vaccines or those convalescent from ancestral wild- type (WT) SARS-CoV-2 (n = 20) or BA.2 infections with (n = 17) or without (n = 7) prior vaccination. RESULTS: Relative to neutralization of the WT virus, those vaccinated with BNT162b2 had 4.8, 3.4, 4.6, 11.3 and 15.5-fold reductions of geometric mean antibody titres (GMT) to BA.1, BA.2, BA.2.12.1, BA.4 and BA.5 viruses, respectively. Similarly, those vaccinated with CoronaVac had 8.0, 7.0, 11.8, 12.0 and 12.0 fold GMT reductions and those with two doses of CoronaVac boosted by BNT162b2 had 6.1, 6.7, 6,3, 13.0 and 21.2 fold GMT reductions to these viruses, respectively. Vaccinated individuals with BA.2 breakthrough infections had higher GMT antibody levels vs. BA.4 (36.9) and BA.5 (36.9) than unvaccinated individuals with BA.2 infections (BA.4 GMT 8.2; BA.5 GMT 11.0). CONCLUSIONS: BA.4 and BA.5 subvariants were less susceptible to BNT162b2 or CoronaVac vaccine elicited antibody neutralization than subvariants BA.1, BA.2 and BA.2.12.1. Nevertheless, three doses BNT162b2 or booster of BNT162b2 following two doses of CoronaVac elicited detectable BA.4 and BA.5 neutralizing antibody responses while those vaccinated with three doses of CoronaVac largely fail to do so. BA.2 infections in vaccinated individuals led to higher levels of BA.4 or BA.5 neutralizing antibody compared to those who were vaccine-naive. The Authors. Published by Elsevier B.V. 2022-11 2022-08-31 /pmc/articles/PMC9428331/ /pubmed/36081282 http://dx.doi.org/10.1016/j.jcv.2022.105273 Text en © 2022 The Authors. Published by Elsevier B.V. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Cheng, Samuel SM
Mok, Chris KP
Li, John KC
Ng, Susanna S
Lam, Bosco HS
Jeevan, Trushar
Kandeil, Ahmed
Pekosz, Andrew
Chan, Karl CK
Tsang, Leo CH
Ko, Fanny W
Chen, Chunke
Yiu, Karen
Luk, Leo LH
Chan, Ken KP
Webby, Richard J
Poon, Leo LM
Hui, David SC
Peiris, Malik
Plaque-neutralizing antibody to BA.2.12.1, BA.4 and BA.5 in individuals with three doses of BioNTech or CoronaVac vaccines, natural infection and breakthrough infection
title Plaque-neutralizing antibody to BA.2.12.1, BA.4 and BA.5 in individuals with three doses of BioNTech or CoronaVac vaccines, natural infection and breakthrough infection
title_full Plaque-neutralizing antibody to BA.2.12.1, BA.4 and BA.5 in individuals with three doses of BioNTech or CoronaVac vaccines, natural infection and breakthrough infection
title_fullStr Plaque-neutralizing antibody to BA.2.12.1, BA.4 and BA.5 in individuals with three doses of BioNTech or CoronaVac vaccines, natural infection and breakthrough infection
title_full_unstemmed Plaque-neutralizing antibody to BA.2.12.1, BA.4 and BA.5 in individuals with three doses of BioNTech or CoronaVac vaccines, natural infection and breakthrough infection
title_short Plaque-neutralizing antibody to BA.2.12.1, BA.4 and BA.5 in individuals with three doses of BioNTech or CoronaVac vaccines, natural infection and breakthrough infection
title_sort plaque-neutralizing antibody to ba.2.12.1, ba.4 and ba.5 in individuals with three doses of biontech or coronavac vaccines, natural infection and breakthrough infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9428331/
https://www.ncbi.nlm.nih.gov/pubmed/36081282
http://dx.doi.org/10.1016/j.jcv.2022.105273
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