Your browser doesn't support javascript.
loading
Immunogenicity of heterologous BNT162b2 booster in fully vaccinated individuals with CoronaVac against SARS-CoV-2 variants Delta and Omicron: the Dominican Republic Experience
Eddy Perez-Then; Carolina Lucas; Valter Silva Monteiro; Marija Miric; Vivian Brache; Leila Cochon; Chantal B.F. Vogels; Elena De la Cruz; Aidelis Jorge; Margarita De los Santos; Patricia Leon; Mallery I. Breban; Kendall Billig; Inci Yildirim; Claire Pearson; Randy Downing; Emily Gagnon; Anthony Muyombwe; Jafar Razeq; Melissa Campbell; Albert Ko; Saad B. Omer; Nathan D Grubaugh; Sten H. Vermund; Akiko Iwasaki.
Afiliação
  • Eddy Perez-Then; Ministry of Health, Santo Domingo, Dominican Republic.
  • Carolina Lucas; Department of Immunobiology, Yale University School of Medicine, New Haven, CT, USA.
  • Valter Silva Monteiro; Department of Immunobiology, Yale University School of Medicine, New Haven, CT, USA.
  • Marija Miric; Two Oceans in Health, Santo Domingo, Dominican Republic.
  • Vivian Brache; Departamento de Investigaciones Biomedicas, Clinica Evangelina Rodriguez, PROFAMILIA. Santo Domingo, Dominican Republic.
  • Leila Cochon; Departamento de Investigaciones Biomedicas, Clinica Evangelina Rodriguez, PROFAMILIA. Santo Domingo, Dominican Republic.
  • Chantal B.F. Vogels; Department of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, CT, USA.
  • Elena De la Cruz; Departamento de Investigaciones Biomedicas, Clinica Evangelina Rodriguez, PROFAMILIA. Santo Domingo, Dominican Republic.
  • Aidelis Jorge; Departamento de Investigaciones Biomedicas, Clinica Evangelina Rodriguez, PROFAMILIA. Santo Domingo, Dominican Republic.
  • Margarita De los Santos; Departamento de Investigaciones Biomedicas, Clinica Evangelina Rodriguez, PROFAMILIA. Santo Domingo, Dominican Republic.
  • Patricia Leon; Laboratorio de Referencia, Dominican Republic.
  • Mallery I. Breban; Department of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, CT, USA.
  • Kendall Billig; Department of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, CT, USA.
  • Inci Yildirim; Department of Pediatric, Section of Infectious Diseases and Global Health; Yale University School of Medicine, New Haven, CT, USA.
  • Claire Pearson; Connecticut State Department of Public Health, Rocky Hill, USA
  • Randy Downing; Connecticut State Department of Public Health, Rocky Hill, USA
  • Emily Gagnon; Connecticut State Department of Public Health, Rocky Hill, USA
  • Anthony Muyombwe; Connecticut State Department of Public Health, Rocky Hill, USA
  • Jafar Razeq; Connecticut State Department of Public Health, Rocky Hill, USA
  • Melissa Campbell; Department of Pediatric, Section of Infectious Diseases and Global Health; Yale University School of Medicine, New Haven, CT, USA.
  • Albert Ko; Yale University School of Public Health
  • Saad B. Omer; Department of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, CT, USA.
  • Nathan D Grubaugh; Yale School of Public Health
  • Sten H. Vermund; Yale School of Public Health, New Haven, CT, USA.
  • Akiko Iwasaki; Yale University School of Medicine
Preprint em Inglês | medRxiv | ID: ppmedrxiv-21268459
ABSTRACT
The recent emergence of the SARS-CoV-2 Omicron variant is raising concerns because of its increased transmissibility and by its numerous spike mutations with potential to evade neutralizing antibodies elicited by COVID-19 vaccines. The Dominican Republic was among the first countries in recommending the administration of a third dose COVID-19 vaccine to address potential waning immunity and reduced effectiveness against variants. Here, we evaluated the effects of a heterologous BNT162b2 mRNA vaccine booster on the humoral immunity of participants that had received a two-dose regimen of CoronaVac, an inactivated vaccine used globally. We found that heterologous CoronaVac prime followed by BNT162b2 booster regimen induces elevated virus-specific antibody levels and potent neutralization activity against the ancestral virus and Delta variant, resembling the titers obtained after two doses of mRNA vaccines. While neutralization of Omicron was undetectable in participants that had received a two-dose regimen of CoronaVac vaccine, BNT162b2 booster resulted in a 1.4-fold increase in neutralization activity against Omicron, compared to two-dose mRNA vaccine. Despite this increase, neutralizing antibody titers were reduced by 6.3-fold and 2.7-fold for Omicron compared to ancestral and Delta variant, respectively. Surprisingly, previous SARS-CoV-2 infection did not affect the neutralizing titers for Omicron in participants that received the heterologous regimen. Our findings have immediate implications for multiples countries that previously used a two-dose regimen of CoronaVac and reinforce the notion that the Omicron variant is associated with immune escape from vaccines or infection-induced immunity, highlighting the global need for vaccine boosters to combat the impact of emerging variants.
Licença
cc_no
Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Experimental_studies Idioma: Inglês Ano de publicação: 2021 Tipo de documento: Preprint
Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Experimental_studies Idioma: Inglês Ano de publicação: 2021 Tipo de documento: Preprint
...