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Neutralizing antibodies against the SARS-CoV-2 Delta and Omicron variants following heterologous CoronaVac plus BNT162b2 booster vaccination.
Pérez-Then, Eddy; Lucas, Carolina; Monteiro, Valter Silva; Miric, Marija; Brache, Vivian; Cochon, Leila; Vogels, Chantal B F; Malik, Amyn A; De la Cruz, Elena; Jorge, Aidelis; De Los Santos, Margarita; Leon, Patricia; Breban, Mallery I; Billig, Kendall; Yildirim, Inci; Pearson, Claire; Downing, Randy; Gagnon, Emily; Muyombwe, Anthony; Razeq, Jafar; Campbell, Melissa; Ko, Albert I; Omer, Saad B; Grubaugh, Nathan D; Vermund, Sten H; Iwasaki, Akiko.
  • Pérez-Then E; Ministry of Health, Santo Domingo, Dominican Republic.
  • Lucas C; Department of Immunobiology, Yale University School of Medicine, New Haven, CT, USA. carolina.lucas@yale.edu.
  • Monteiro VS; Department of Immunobiology, Yale University School of Medicine, New Haven, CT, USA.
  • Miric M; Two Oceans in Health, Santo Domingo, Dominican Republic.
  • Brache V; Biomedical Research Department, Profamilia, Santo Domingo, Dominican Republic.
  • Cochon L; Biomedical Research Department, Profamilia, Santo Domingo, Dominican Republic.
  • Vogels CBF; Department of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, CT, USA.
  • Malik AA; Yale Institute for Global Health, Yale University, New Haven, CT, USA.
  • De la Cruz E; Section of Infectious Diseases, Department of Medicine, Yale University School of Medicine, New Haven, CT, USA.
  • Jorge A; Biomedical Research Department, Profamilia, Santo Domingo, Dominican Republic.
  • De Los Santos M; Biomedical Research Department, Profamilia, Santo Domingo, Dominican Republic.
  • Leon P; Biomedical Research Department, Profamilia, Santo Domingo, Dominican Republic.
  • Breban MI; Laboratorio de Referencia, Santo Domingo, Dominican Republic.
  • Billig K; Department of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, CT, USA.
  • Yildirim I; Department of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, CT, USA.
  • Pearson C; Department of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, CT, USA.
  • Downing R; Yale Institute for Global Health, Yale University, New Haven, CT, USA.
  • Gagnon E; Section of Infectious Diseases and Global Health, Department of Pediatrics, Yale University School of Medicine, New Haven, CT, USA.
  • Muyombwe A; Connecticut State Department of Public Health, Rocky Hill, CT, USA.
  • Razeq J; Connecticut State Department of Public Health, Rocky Hill, CT, USA.
  • Campbell M; Connecticut State Department of Public Health, Rocky Hill, CT, USA.
  • Ko AI; Connecticut State Department of Public Health, Rocky Hill, CT, USA.
  • Omer SB; Connecticut State Department of Public Health, Rocky Hill, CT, USA.
  • Grubaugh ND; Section of Infectious Diseases and Global Health, Department of Pediatrics, Yale University School of Medicine, New Haven, CT, USA.
  • Vermund SH; Department of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, CT, USA.
  • Iwasaki A; Section of Infectious Diseases, Department of Medicine, Yale University School of Medicine, New Haven, CT, USA.
Nat Med ; 28(3): 481-485, 2022 03.
Article in English | MEDLINE | ID: covidwho-1636460
ABSTRACT
The recent emergence of the SARS-CoV-2 Omicron variant is raising concerns because of its increased transmissibility and its numerous spike mutations, which have the potential to evade neutralizing antibodies elicited by COVID-19 vaccines. Here we evaluated the effects of a heterologous BNT162b2 mRNA vaccine booster on the humoral immunity of participants who had received a two-dose regimen of CoronaVac, an inactivated vaccine used globally. We found that a heterologous CoronaVac prime vaccination of two doses followed by a BNT162b2 booster induces elevated virus-specific antibody levels and potent neutralization activity against the ancestral virus and the Delta variant, resembling the titers obtained after two doses of mRNA vaccines. Although neutralization of Omicron was undetectable in participants who had received a two-dose regimen of CoronaVac, the BNT162b2 booster resulted in a 1.4-fold increase in neutralization activity against Omicron compared with the two-dose mRNA vaccine. Despite this increase, neutralizing antibody titers were reduced by 7.1-fold and 3.6-fold for Omicron compared with the ancestral strain and the Delta variant, respectively. These findings have immediate implications for multiple countries that previously used a CoronaVac regimen and reinforce the idea 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.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 / BNT162 Vaccine Type of study: Experimental Studies Topics: Vaccines / Variants Limits: Humans Language: English Journal: Nat Med Journal subject: Molecular Biology / Medicine Year: 2022 Document Type: Article Affiliation country: S41591-022-01705-6

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 / BNT162 Vaccine Type of study: Experimental Studies Topics: Vaccines / Variants Limits: Humans Language: English Journal: Nat Med Journal subject: Molecular Biology / Medicine Year: 2022 Document Type: Article Affiliation country: S41591-022-01705-6