
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
2022; Frontiers Media; Volume: 13; Linguagem: Inglês
10.3389/fimmu.2022.918896
ISSN1664-3224
AutoresRafaella Fortini Queiroz Grenfell, Nathalie Bonatti Franco Almeida, Priscilla Soares Filgueiras, Camila Amormino Corsini, Sarah Vieira Contin Gomes, Daniel Alvim Pena de Miranda, Adelina J. Lourenço, Olindo Assis Martins‐Filho, Jaquelline Germano de Oliveira, Andréa Teixeira‐Carvalho, Guilherme Rodrigues Fernandes Campos, Maurício Lacerda Nogueira, Pedro Augusto Alves, Gabriel da Rocha Fernandes, Leda R. Castilho, Túlio M. Lima, Daniel Paiva Barros de Abreu, Renata G. F. Alvim, Thaís Bárbara de S. Silva, Wander de Jesus Jeremias, Dayane Andriotti Otta, Ana Carolina Campi‐Azevedo,
Tópico(s)SARS-CoV-2 detection and testing
ResumoBackground 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.
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