Humoral anti-SARS-CoV-2 immune response for different strains after Sinovac-CoronaVac and Oxford/AstraZeneca (ChAdOx1-S) full vaccination on a healthcare population in Brazil
Autor(a) principal: | |
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Data de Publicação: | 2024 |
Outros Autores: | , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | por eng |
Título da fonte: | Revista Uningá (Online) |
Texto Completo: | https://revista.uninga.br/uninga/article/view/4570 |
Resumo: | COVID-19, caused by the SARS-CoV-2 virus, is a global respiratory syndrome with high mortality rates. Vaccination is currently the only proven method to prevent the disease, although the role of lab data in assessing efficacy remains uncertain. This study aimed to assess spike-binding and neutralizing antibody levels following full vaccination with Oxford/AstraZeneca (ChAdOx1 nCoV-19) or CoronaVac in healthcare workers in southeastern Brazil. ChAdOx1 nCoV-19 and CoronaVac induced IgG antibodies against trimeric spike glycoproteins in 99.5% and 80.9% of individuals, respectively. Neutralizing antibodies were produced against two viral strains groups: variants group 1 (Wuhan-Hu-1, Alpha) and variants group 2 (Beta, Gamma) with neutralization rates of 88.3% and 78.2% for ChAdOx1 nCoV-19, and 68.1% and 48.9% for CoronaVac. No associations were found between neutralizing levels and comorbidities, age, or side effects. A positive correlation was observed between IgG antibody concentrations against trimeric spike glycoproteins and neutralizing levels for both vaccines and variants. These findings indicate that both vaccines induced reasonable levels of neutralizing antibodies against variants group 1, but only ChAdOx1 nCoV-19 maintained acceptable levels against a variant strain. The study suggests that evaluating vaccine responses to different pathogen strains can aid in managing healthcare workforce concerns and improve vaccine selection, thereby enhancing overall vaccination strategies. |
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Humoral anti-SARS-CoV-2 immune response for different strains after Sinovac-CoronaVac and Oxford/AstraZeneca (ChAdOx1-S) full vaccination on a healthcare population in BrazilResposta imune humoral anti-SARS-CoV-2 para diferentes cepas virais após vacinação completa com Sinovac-CoronaVac e Oxford/AstraZeneca (ChAdOx1-S) em uma população de trabalhadores da saúde no BrasilChAdOx1 nCoV-19CoronaVacCOVID-19 vaccinesneutralizing antibodiesSARS-CoV-2.CoronavirusCOVID-19Healthcare WorkersOccupational healthHealthVaccineAnticorpos neutralizantesChAdOx1 nCoV-19CoronaVacSARS-CoV-2vacinas contra Covid-19.CoronavírusCovid-19Profissionais de saúde Saúde ocupacional Saúde VacinaCOVID-19, caused by the SARS-CoV-2 virus, is a global respiratory syndrome with high mortality rates. Vaccination is currently the only proven method to prevent the disease, although the role of lab data in assessing efficacy remains uncertain. This study aimed to assess spike-binding and neutralizing antibody levels following full vaccination with Oxford/AstraZeneca (ChAdOx1 nCoV-19) or CoronaVac in healthcare workers in southeastern Brazil. ChAdOx1 nCoV-19 and CoronaVac induced IgG antibodies against trimeric spike glycoproteins in 99.5% and 80.9% of individuals, respectively. Neutralizing antibodies were produced against two viral strains groups: variants group 1 (Wuhan-Hu-1, Alpha) and variants group 2 (Beta, Gamma) with neutralization rates of 88.3% and 78.2% for ChAdOx1 nCoV-19, and 68.1% and 48.9% for CoronaVac. No associations were found between neutralizing levels and comorbidities, age, or side effects. A positive correlation was observed between IgG antibody concentrations against trimeric spike glycoproteins and neutralizing levels for both vaccines and variants. These findings indicate that both vaccines induced reasonable levels of neutralizing antibodies against variants group 1, but only ChAdOx1 nCoV-19 maintained acceptable levels against a variant strain. The study suggests that evaluating vaccine responses to different pathogen strains can aid in managing healthcare workforce concerns and improve vaccine selection, thereby enhancing overall vaccination strategies.A Covid-19, causada pelo vírus SARS-CoV-2, é uma síndrome respiratória global com altas taxas de mortalidade. A vacinação é atualmente o único método comprovado para prevenir a doença, embora o papel dos dados laboratoriais na avaliação da eficácia ainda seja incerto. Este estudo teve como objetivo avaliar os níveis de anticorpos anti-spike e anticorpos neutralizantes após a vacinação completa com Oxford/AstraZeneca (ChAdOx1 nCoV-19) ou CoronaVac em profissionais de saúde no sudeste do Brasil. ChAdOx1 nCoV-19 e CoronaVac induziram anticorpos IgG contra glicoproteína spike (S) em 99,5% e 80,9% dos indivíduos, respectivamente. Anticorpos neutralizantes foram produzidos contra dois grupos de cepas virais: grupo de variantes 1 (Wuhan-Hu-1, Alfa) e grupo de variantes 2 (Beta, Gama), com taxas de neutralização de 88,3% e de 78,2% para ChAdOx1 nCoV-19, de 68,1% e de 48,9% para CoronaVac. Não foram encontradas associações entre os níveis de neutralização e de comorbidades, de idade ou de efeitos colaterais. Observou-se correlação positiva entre as concentrações de anticorpos IgG contra glicoproteínas spike (S) e os níveis de neutralização para ambas as vacinas e as variantes. Estes resultados indicam que ambas as vacinas induziram níveis razoáveis de anticorpos neutralizantes contra variantes do grupo 1, mas apenas ChAdOx1 nCoV-19 manteve níveis aceitáveis contra uma cepa variante. O estudo sugere que a avaliação das respostas vacinais a diferentes cepas patogênicas pode auxiliar no gerenciamento das preocupações da força de trabalho em saúde e melhorar a seleção de vacinas para pacientes específicos, melhorando, assim, as estratégias gerais de vacinação.Editora Uningá2024-03-14info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionTextoinfo:eu-repo/semantics/otherapplication/pdfapplication/pdftext/xmlhttps://revista.uninga.br/uninga/article/view/457010.46311/2318-0579.61.eUJ4570Revista Uningá; Vol. 61 (2024); eUJ4570Revista Uningá; v. 61 (2024); eUJ45702318-0579reponame:Revista Uningá (Online)instname:Centro Universitário Uningáinstacron:UNINGAporenghttps://revista.uninga.br/uninga/article/view/4570/2718https://revista.uninga.br/uninga/article/view/4570/2721https://revista.uninga.br/uninga/article/view/4570/2722Copyright (c) 2024 Revista Uningáhttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessOliveira, Maicon Jeferson Silva de Nascimento, Beatriz Birelli do Oliveira, Fernanda de Assis Mahelly Bueno de AlmeidaRodrigues, Márcio Carvalho, Flavia Cristina Cardoso Barioni, Éric Diego Loiola, Rodrigo Azevedo Oliveira, Rômulo Tadeu Dias de Rocha, Gustavo Henrique Oliveira da 2024-04-01T13:31:42Zoai:ojs.revista.uninga.br:article/4570Revistahttps://revista.uninga.br/uninga/indexPUBhttps://revista.uninga.br/uninga/oairevistauninga@uninga.edu.br2318-05792318-0579opendoar:2024-04-01T13:31:42Revista Uningá (Online) - Centro Universitário Uningáfalse |
dc.title.none.fl_str_mv |
Humoral anti-SARS-CoV-2 immune response for different strains after Sinovac-CoronaVac and Oxford/AstraZeneca (ChAdOx1-S) full vaccination on a healthcare population in Brazil Resposta imune humoral anti-SARS-CoV-2 para diferentes cepas virais após vacinação completa com Sinovac-CoronaVac e Oxford/AstraZeneca (ChAdOx1-S) em uma população de trabalhadores da saúde no Brasil |
title |
Humoral anti-SARS-CoV-2 immune response for different strains after Sinovac-CoronaVac and Oxford/AstraZeneca (ChAdOx1-S) full vaccination on a healthcare population in Brazil |
spellingShingle |
Humoral anti-SARS-CoV-2 immune response for different strains after Sinovac-CoronaVac and Oxford/AstraZeneca (ChAdOx1-S) full vaccination on a healthcare population in Brazil Oliveira, Maicon Jeferson Silva de ChAdOx1 nCoV-19 CoronaVac COVID-19 vaccines neutralizing antibodies SARS-CoV-2. Coronavirus COVID-19 Healthcare Workers Occupational health Health Vaccine Anticorpos neutralizantes ChAdOx1 nCoV-19 CoronaVac SARS-CoV-2 vacinas contra Covid-19. Coronavírus Covid-19 Profissionais de saúde Saúde ocupacional Saúde Vacina |
title_short |
Humoral anti-SARS-CoV-2 immune response for different strains after Sinovac-CoronaVac and Oxford/AstraZeneca (ChAdOx1-S) full vaccination on a healthcare population in Brazil |
title_full |
Humoral anti-SARS-CoV-2 immune response for different strains after Sinovac-CoronaVac and Oxford/AstraZeneca (ChAdOx1-S) full vaccination on a healthcare population in Brazil |
title_fullStr |
Humoral anti-SARS-CoV-2 immune response for different strains after Sinovac-CoronaVac and Oxford/AstraZeneca (ChAdOx1-S) full vaccination on a healthcare population in Brazil |
title_full_unstemmed |
Humoral anti-SARS-CoV-2 immune response for different strains after Sinovac-CoronaVac and Oxford/AstraZeneca (ChAdOx1-S) full vaccination on a healthcare population in Brazil |
title_sort |
Humoral anti-SARS-CoV-2 immune response for different strains after Sinovac-CoronaVac and Oxford/AstraZeneca (ChAdOx1-S) full vaccination on a healthcare population in Brazil |
author |
Oliveira, Maicon Jeferson Silva de |
author_facet |
Oliveira, Maicon Jeferson Silva de Nascimento, Beatriz Birelli do Oliveira, Fernanda de Assis Mahelly Bueno de Almeida Rodrigues, Márcio Carvalho, Flavia Cristina Cardoso Barioni, Éric Diego Loiola, Rodrigo Azevedo Oliveira, Rômulo Tadeu Dias de Rocha, Gustavo Henrique Oliveira da |
author_role |
author |
author2 |
Nascimento, Beatriz Birelli do Oliveira, Fernanda de Assis Mahelly Bueno de Almeida Rodrigues, Márcio Carvalho, Flavia Cristina Cardoso Barioni, Éric Diego Loiola, Rodrigo Azevedo Oliveira, Rômulo Tadeu Dias de Rocha, Gustavo Henrique Oliveira da |
author2_role |
author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Oliveira, Maicon Jeferson Silva de Nascimento, Beatriz Birelli do Oliveira, Fernanda de Assis Mahelly Bueno de Almeida Rodrigues, Márcio Carvalho, Flavia Cristina Cardoso Barioni, Éric Diego Loiola, Rodrigo Azevedo Oliveira, Rômulo Tadeu Dias de Rocha, Gustavo Henrique Oliveira da |
dc.subject.por.fl_str_mv |
ChAdOx1 nCoV-19 CoronaVac COVID-19 vaccines neutralizing antibodies SARS-CoV-2. Coronavirus COVID-19 Healthcare Workers Occupational health Health Vaccine Anticorpos neutralizantes ChAdOx1 nCoV-19 CoronaVac SARS-CoV-2 vacinas contra Covid-19. Coronavírus Covid-19 Profissionais de saúde Saúde ocupacional Saúde Vacina |
topic |
ChAdOx1 nCoV-19 CoronaVac COVID-19 vaccines neutralizing antibodies SARS-CoV-2. Coronavirus COVID-19 Healthcare Workers Occupational health Health Vaccine Anticorpos neutralizantes ChAdOx1 nCoV-19 CoronaVac SARS-CoV-2 vacinas contra Covid-19. Coronavírus Covid-19 Profissionais de saúde Saúde ocupacional Saúde Vacina |
description |
COVID-19, caused by the SARS-CoV-2 virus, is a global respiratory syndrome with high mortality rates. Vaccination is currently the only proven method to prevent the disease, although the role of lab data in assessing efficacy remains uncertain. This study aimed to assess spike-binding and neutralizing antibody levels following full vaccination with Oxford/AstraZeneca (ChAdOx1 nCoV-19) or CoronaVac in healthcare workers in southeastern Brazil. ChAdOx1 nCoV-19 and CoronaVac induced IgG antibodies against trimeric spike glycoproteins in 99.5% and 80.9% of individuals, respectively. Neutralizing antibodies were produced against two viral strains groups: variants group 1 (Wuhan-Hu-1, Alpha) and variants group 2 (Beta, Gamma) with neutralization rates of 88.3% and 78.2% for ChAdOx1 nCoV-19, and 68.1% and 48.9% for CoronaVac. No associations were found between neutralizing levels and comorbidities, age, or side effects. A positive correlation was observed between IgG antibody concentrations against trimeric spike glycoproteins and neutralizing levels for both vaccines and variants. These findings indicate that both vaccines induced reasonable levels of neutralizing antibodies against variants group 1, but only ChAdOx1 nCoV-19 maintained acceptable levels against a variant strain. The study suggests that evaluating vaccine responses to different pathogen strains can aid in managing healthcare workforce concerns and improve vaccine selection, thereby enhancing overall vaccination strategies. |
publishDate |
2024 |
dc.date.none.fl_str_mv |
2024-03-14 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion Texto info:eu-repo/semantics/other |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://revista.uninga.br/uninga/article/view/4570 10.46311/2318-0579.61.eUJ4570 |
url |
https://revista.uninga.br/uninga/article/view/4570 |
identifier_str_mv |
10.46311/2318-0579.61.eUJ4570 |
dc.language.iso.fl_str_mv |
por eng |
language |
por eng |
dc.relation.none.fl_str_mv |
https://revista.uninga.br/uninga/article/view/4570/2718 https://revista.uninga.br/uninga/article/view/4570/2721 https://revista.uninga.br/uninga/article/view/4570/2722 |
dc.rights.driver.fl_str_mv |
Copyright (c) 2024 Revista Uningá https://creativecommons.org/licenses/by/4.0 info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
Copyright (c) 2024 Revista Uningá https://creativecommons.org/licenses/by/4.0 |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf application/pdf text/xml |
dc.publisher.none.fl_str_mv |
Editora Uningá |
publisher.none.fl_str_mv |
Editora Uningá |
dc.source.none.fl_str_mv |
Revista Uningá; Vol. 61 (2024); eUJ4570 Revista Uningá; v. 61 (2024); eUJ4570 2318-0579 reponame:Revista Uningá (Online) instname:Centro Universitário Uningá instacron:UNINGA |
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Centro Universitário Uningá |
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UNINGA |
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UNINGA |
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Revista Uningá (Online) |
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Revista Uningá (Online) |
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Revista Uningá (Online) - Centro Universitário Uningá |
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revistauninga@uninga.edu.br |
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