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Neutralization of VOCs including Delta one year post COVID-19 or vaccine
Sebastian Havervall; Ulrika Marking; Max Gordon; Henry Ng; Nina Greilert-Norin; Sarah Lindbo; Kim Blom; Peter Nilsson; Mia Phillipson; Jonas Klingstrom; Sara Mangsbo; Mikael Aberg; Sophia Hober; Charlotte Thalin.
Affiliation
  • Sebastian Havervall; Karolinska Institutet Danderyd Hospital, Stockholm, Sweden
  • Ulrika Marking; Karolinska Institutet Danderyd Hospital, Stockholm, Sweden
  • Max Gordon; Karolinska Institutet Danderyd Hospital, Stockholm, Sweden
  • Henry Ng; Department of Medical Cell Biology and Science for Life Laboratory, Uppsala University, Uppsala, Sweden
  • Nina Greilert-Norin; Karolinska Institutet Danderyd Hospital, Stockholm, Sweden
  • Sarah Lindbo; Department of Protein Science, KTH Royal Institute of Technology, SciLifeLab, Stockholm, Sweden
  • Kim Blom; Public Health Agency of Sweden, Solna, Sweden
  • Peter Nilsson; Department of Protein Science, KTH Royal Institute of Technology, SciLifeLab, Stockholm, Sweden
  • Mia Phillipson; Department of Medical Cell Biology and Science for Life Laboratory, Uppsala University, Uppsala, Sweden
  • Jonas Klingstrom; Center for Infectious Medicine, Department of Medicine, Karolinska Institutet, Karolinska University Hospital Huddinge, Stockholm, Sweden
  • Sara Mangsbo; Department of Pharmaceutical Biosciences and Science for Life Laboratory, Uppsala University, Uppsala, Sweden
  • Mikael Aberg; Department of Medical Sciences, Clinical Chemistry and Science for Life Laboratory, Uppsala University, Uppsala, Sweden
  • Sophia Hober; Department of Protein Science, KTH Royal Institute of Technology, SciLifeLab, Stockholm, Sweden
  • Charlotte Thalin; Danderyd Hospital, Karolinska Institute, Stockholm, Sweden
Preprint in English | medRxiv | ID: ppmedrxiv-21261951
ABSTRACT
BackgroundSARS-CoV-2 variants, such as Alpha, Beta, Gamma and Delta, are raising concern about the efficiency of neutralizing antibodies (NAb) induced by wild-type infection or vaccines based on the wild-type spike. MethodsWe determined IgG and NAb against SARS-CoV-2 variants one year following mild wild-type infection (n=104) and two-dose regimens with BNT162b2 (BNT/BNT) (n=67), ChAdOx1 (ChAd/ChAd) (n=82), or heterologous ChAdOx1 followed by BNT162b2 (ChAd/BNT) (n=116). FindingsWild type spike IgG and NAb remained detectable in 80% (83/104) of unvaccinated participants one year post mild infection. The neutralizing capacity was similar against wild type (reference), Alpha (0.95 (0.92-0.98) and Delta 1.03 (0.95-1.11) but significantly reduced against Beta (0.54 (0.48-0.60)) and Gamma 0.51 (0.44-0.61). Similarly, BNT/BNT and ChAd/ChAd elicited sustained capacity against Alpha and Delta (1.01 (0.78-1.31) and 0.85 (0.64-1.14)) and (0.96 (0.84-1.09) and 0.82 (0.61-1.10) respectively), with reduced capacity against Beta (0.67 (0.50-0.88) and 0.53 (0.40-0.71)) and Gamma (0.12 (0.06-0.27) and 0.54 (0.37-0.80)). A similar trend was found following ChAd/BNT (0.74 (0.66-0.83) and 0.70 (0.50-0.97) against Alpha and Delta and 0.29 (0.20-0.42) and 0.13 (0.08-0.20) against Beta and Gamma). InterpretationPersistent neutralization of the wide-spread Alpha and Delta variants one year after wild-type infection may aid vaccine policy makers in low-resource settings when prioritizing vaccine supply. The reduced capacity of neutralizing Beta and Gamma strains, but not the Alpha and Delta strains following both infection and three different vaccine regimens argues for caution against Beta and Gamma-exclusive mutations in the efforts to optimize next generation SARS-CoV-2 vaccines. FundingA full list of funding bodies that contributed to this study can be found in the Acknowledgements section
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Full text: Available Collection: Preprints Database: medRxiv Language: English Year: 2021 Document type: Preprint
Full text: Available Collection: Preprints Database: medRxiv Language: English Year: 2021 Document type: Preprint
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