Article
Protective Immunity against Gamma and Zeta Variants after Inactivated SARS-CoV-2 Virus Immunization.
Registro en:
FUMAGALLI, Marcilio Jorge et al. Protective Immunity against Gamma and Zeta Variants after Inactivated SARS-CoV-2 Virus Immunization. Viruses ; v. 13, n. 12, 2021, 2440. doi: 10.3390/v13122440
1999-4915
10.3390/v13122440
Autor
Fumagalli, Marcilio Jorge
Castro-Jorge, Luiza Antunes
Fraga-Silva, Thais Fernanda de Campos
de Azevedo, Patrick Orestes
Capato, Carlos Fabiano
Rattis, Bruna Amanda Cruz
Hojo-Souza, Natália Satchiko
Floriano, Vitor Gonçalves
de Castro, Julia Teixeira
Ramos, Simone Gusmão
da Fonseca, Benedito Antônio Lopes
Bonato, Vânia Luiza Deperon
Gazzinelli, Ricardo Tostes
Figueiredo, Luiz Tadeu Moraes.
Resumen
The persistent circulation of SARS-CoV-2 represents an ongoing global threat due to the emergence of new viral variants that can sometimes evade the immune system of previously exposed or vaccinated individuals. We conducted a follow-up study of adult individuals that had received an inactivated SARS-CoV-2 vaccine, evaluating antibody production and neutralizing activity over a period of 6 months. In addition, we performed mice immunization with inactivated SARS-CoV-2, and evaluated the immune response and pathological outcomes against Gamma and Zeta variant infection. Vaccinated individuals produced high levels of antibodies with robust neutralizing activity, which was significantly reduced against Gamma and Zeta variants. Production of IgG anti-S antibodies and neutralizing activity robustly reduced after 6 months of vaccination. Immunized mice demonstrated cellular response against Gamma and Zeta variants, and after viral infection, reduced viral loads, IL-6 expression, and histopathological outcome in the lungs. TNF levels were unchanged in immunized or not immunized mice after infection with the Gamma variant. Furthermore, serum neutralization activity rapidly increases after infection with the Gamma and Zeta variants. Our data suggest that immunization with inactivated WT SARS-CoV-2 induces a promptly responsive cross-reactive immunity response against the Gamma and Zeta variants, reducing COVID-19 pathological outcomes.