Use este identificador para citar ou linkar para este item: http://www.repositorio.ufop.br/jspui/handle/123456789/17627
Título: Immunogenicity, effectiveness, and safety of inactivated virus (CoronaVac) vaccine in a two-dose primary protocol and BNT162b2 heterologous booster in Brazil (Immunita-001) : a one year period follow up phase 4 study.
Autor(es): Grenfell, Rafaella Fortini Queiroz
Almeida, Nathalie Bonatti Franco
Filgueiras, Priscilla Soares
Corsini, Camila Amormino
Gomes, Sarah Vieira Contin
Miranda, Daniel Alvim Pena de
Lourenço, Adelina Junia
Martins Filho, Olindo Assis
Oliveira, Jaquelline Germano de
Carvalho, Andréa Teixeira de
Campos, Guilherme Rodrigues Fernandes
Nogueira, Maurício Lacerda
Alves, Pedro Augusto
Fernandes, Gabriel da Rocha
Castilho, Leda dos Reis
Lima, Túlio Macedo
Abreu, Daniel Paiva Barros de
Alvim, Renata Guimarães Ferreira
Silva, Thaís Bárbara de Souza
Jeremias, Wander de Jesus
Otta, Dayane Andriotti
Azevedo, Ana Carolina Campi
Immunita-001 Team
Palavras-chave: SARS-CoV-2
Covid-19
Immune response
Data do documento: 2022
Referência: GRENFELL, R. F. Q. et al. Immunogenicity, effectiveness, and safety of inactivated virus (CoronaVac) vaccine in a two-dose primary protocol and BNT162b2 heterologous booster in Brazil (Immunita-001): a one year period follow up phase 4 study. Frontiers in Immunology, v. 13, 2022. Disponível em: <https://www.frontiersin.org/articles/10.3389/fimmu.2022.918896/full>. Acesso em: 01 ago. 2023.
Resumo: Background: Effective and safe vaccines against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are critical to controlling the COVID-19 pandemic and will remain the most important tool in limiting the spread of the virus long after the pandemic is over. Methods: We bring pioneering contributions on the maintenance of the immune response over a year on a real-life basis study in 1,587 individuals (18-90 yrs, median 39 yrs; 1,208 female/379 male) who underwent vaccination with two doses of CoronaVac and BNT162b2 booster after 6-months of primary protocol. Findings: Elevated levels of anti-spike IgG antibodies were detected after CoronaVac vaccination, which significantly decreased after 80 days and remained stable until the introduction of the booster dose. Heterologous booster restored antibody titers up to-1·7- fold, changing overall seropositivity to 96%. Titers of neutralising antibodies to the Omicron variant were lower in all timepoints than those against Delta variant. Individuals presenting neutralising antibodies against Omicron also presented the highest titers against Delta and anti-Spike IgG. Cellular immune response measurement pointed out a mixed immune profile with a robust release of chemokines, cytokines, and growth factors on the first month after CoronaVac vaccination followed by a gradual reduction over time and no increase after the booster dose. A stronger interaction between those mediators was noted over time. Prior exposure to the virus leaded to a more robust cellular immune response and a rise in antibody levels 60 days post CoronaVac than in individuals with no previous COVID-19. Both vaccines were safe and well tolerated among individuals. Interpretation: Our data approach the effectiveness of CoronaVac association with BNT162b2 from the clinical and biological perspectives, aspects that have important implications for informing decisions about vaccine boosters. Funding: Fiocruz, Brazil.
URI: http://www.repositorio.ufop.br/jspui/handle/123456789/17627
DOI: https://doi.org/10.3389/fimmu.2022.918896
ISSN: 1664-3224
Licença: This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. Fonte: PDF do artigo.
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