Protective Immunity against Gamma and Zeta Variants after Inactivated SARS-CoV-2 Virus Immunization.
Marcilio Jorge FumagalliLuiza Antunes Castro-JorgeThais Fernanda de Campos Fraga-SilvaPatrick Orestes de AzevedoCarlos Fabiano CapatoBruna Amanda Cruz RattisNatália Satchiko Hojo-SouzaVitor Gonçalves FlorianoJulia Teixeira de CastroSimone Gusmão RamosBenedito Antônio Lopes da FonsecaVania Luiza Deperon BonatoRicardo Tostes GazzinelliLuiz Tadeu Moraes FigueiredoPublished in: Viruses (2021)
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.
Keyphrases
- sars cov
- copy number
- respiratory syndrome coronavirus
- immune response
- high fat diet induced
- rheumatoid arthritis
- type diabetes
- dengue virus
- gene expression
- young adults
- coronavirus disease
- genome wide
- adipose tissue
- dna methylation
- zika virus
- electronic health record
- machine learning
- toll like receptor
- big data
- skeletal muscle
- artificial intelligence