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

被引:14
|
作者
Grenfell, Rafaella F. Q. [1 ,2 ]
Almeida, Nathalie B. F. [1 ,2 ]
Filgueiras, Priscilla S. [1 ]
Corsini, Camila A. [1 ]
Gomes, Sarah V. C. [1 ]
de Miranda, Daniel A. P. [1 ]
Lourenco, Adelina J. [3 ]
Martins-Filho, Olindo A. [4 ]
de Oliveira, Jaquelline G. [5 ]
Teixeira-Carvalho, Andrea [4 ]
Campos, Guilherme R. F. [6 ]
Nogueira, Mauricio L. [6 ,7 ,8 ]
Alves, Pedro Augusto [9 ]
Fernandes, Gabriel R. [1 ,10 ]
Castilho, Leda R. [11 ]
Lima, Tulio M. [11 ]
de Abreu, Daniel P. B. [11 ]
Alvim, Renata G. F. [11 ]
Silva, Thais Barbara de S. [9 ]
Jeremias, Wander de J. [12 ]
Otta, Dayane A. [4 ]
Campi-Azevedo, Ana Carolina [4 ]
机构
[1] Oswaldo Cruz Fdn Fiocruz, Diag & Therapy Infect Dis & Canc, Belo Horizonte, MG, Brazil
[2] Univ Georgia, Coll Vet Med, Dept Infect Dis, Athens, GA 30602 USA
[3] Hosp Baleia, Benjamin Guimaraes Fdn, Belo Horizonte, MG, Brazil
[4] Oswaldo Cruz Fdn Fiocruz, Grp Integrad Pesquisa Biomarcadores, Belo Horizonte, MG, Brazil
[5] Oswaldo Cruz Fdn Fiocruz, Lab Imunol Celular & Mol, Belo Horizonte, MG, Brazil
[6] Fac Med Sao Jose do Rio Preto FAMERP, Lab Pesquisas Virol LPV, Sao Jose Do Rio Preto, Brazil
[7] Hosp Base, Sao Jose Do Rio Preto, Brazil
[8] Univ Texas Med Branch, Dept Pathol, Galveston, TX 77555 USA
[9] Oswaldo Cruz Fdn Fiocruz, Imunol Doencas Virais, Belo Horizonte, MG, Brazil
[10] Oswaldo Cruz Fdn Fiocruz, Biosyst Informat, Belo Horizonte, MG, Brazil
[11] Univ Fed Rio de Janeiro, Cell Culture Engn Lab COPPE, Rio De Janeiro, Brazil
[12] Univ Fed Ouro Preto, Coll Pharm, Lab Farmacol Expt, Ouro Preto, Brazil
来源
FRONTIERS IN IMMUNOLOGY | 2022年 / 13卷
基金
美国国家卫生研究院; 巴西圣保罗研究基金会;
关键词
SARS-CoV-2; COVID-19; vaccine; immune response; coronavac; BNT162b2; heterologous booster;
D O I
10.3389/fimmu.2022.918896
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
BackgroundEffective 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. MethodsWe 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. FindingsElevated 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 center dot 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. InterpretationOur 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. FundingFiocruz, Brazil.
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页数:13
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