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Cross reactivity of spike glycoprotein induced antibody against delta and omicron variants before and after third SARS-CoV-2 vaccine dose
Sian E Faustini; Adrian M Shields; Gemma Banham; Nadezhda Wall; Saly Al-Taei; Chloe Tanner; Zahra Ahmed; Elena Efstathiou; Neal Townsend; Ruth Price; Grace Curry; Louise Robertson; Andrew Nesbit; Amy Black; JULIE MOORE; James McLaughlin; John Farnan; - COVID-HD Birmingham Study Group; - PITCH consortium; Adam F Cunningham; Lorraine Harper; Tara Moore; Mark T Drayson; Alex G Richter.
Afiliação
  • Sian E Faustini; Institute of Immunology and Immunotherapy, University of Birmingham
  • Adrian M Shields; Institute of Immunology and Immunotherapy, University of Birmingham
  • Gemma Banham; Institute of Clinical Sciences, University of Birmingham
  • Nadezhda Wall; Institute of Clinical Sciences, University of Birmingham
  • Saly Al-Taei; Institute of Immunology and Immunotherapy, University of Birmingham
  • Chloe Tanner; Institute of Immunology and Immunotherapy, University of Birmingham
  • Zahra Ahmed; Institute of Immunology and Immunotherapy, University of Birmingham
  • Elena Efstathiou; Institute of Immunology and Immunotherapy, University of Birmingham
  • Neal Townsend; Institute of Immunology and Immunotherapy, University of Birmingham
  • Ruth Price; Biomedical Sciences Research Institute, Ulster University, Northern Ireland
  • Grace Curry; Biomedical Sciences Research Institute, Ulster University, Northern Ireland
  • Louise Robertson; Biomedical Sciences Research Institute, Ulster University, Northern Ireland
  • Andrew Nesbit; Biomedical Sciences Research Institute, Ulster University, Northern Ireland
  • Amy Black; Biomedical Sciences Research Institute, Ulster University, Northern Ireland
  • JULIE MOORE; Biomedical Sciences Research Institute, Ulster University, Northern Ireland
  • James McLaughlin; Nanotechnology and Integrated Bioengineering Centre, Ulster University, Northern Ireland
  • John Farnan; The Group Surgery, 257 North Queen Street, Belfast, Northern Ireland
  • - COVID-HD Birmingham Study Group;
  • - PITCH consortium;
  • Adam F Cunningham; Immunology and Immunotherapy, University of Birmingham
  • Lorraine Harper; Institute of Inflammation and Ageing, University of Birmingham
  • Tara Moore; Biomedical Sciences Research Institute, Ulster University, Northern Ireland
  • Mark T Drayson; Institute of Immunology and Immunotherapy, University of Birmingham
  • Alex G Richter; Institute of Immunology and Immunotherapy, University of Birmingham
Preprint em En | PREPRINT-MEDRXIV | ID: ppmedrxiv-21268308
ABSTRACT
Variants of SARS-CoV-2 may evade natural and vaccine induced immunity and monoclonal antibody immunotherapeutics. There is an urgent need to know how well antibodies, induced by healthy and Clinically Extremely Vulnerable (CEV) patients, will bind and thus help reduce transmission and severity of infection from variants of concern (VOC). This study determines the cross-reactive binding of serum antibodies obtained prior to and 28 days after a third vaccination in three cohorts; a health care worker cohort who received three doses of Pfizer-BioNtech (PPP), a cohort of CEV patients received two doses of the AstraZeneca-ChAdOx1-nCoV-19 (AAP) vaccine, followed by a third PFZ vaccine and a haemodialysis cohort that had a mixture of two AZ or PFZ vaccines followed by a PFZ booster. Six months post second vaccine there was evidence of antibody waning with 58.9% of individuals in the HD cohort seropositive against Wuhan, 34.4% Delta and 62.2% Omicron strains. For the AAP cohort, equivalent figures were 62.5%, 45.8% and 91.7% and the PPP cohort 92.2%, 90% and 91.1%. Post third dose vaccination there were universal increases in seropositivity and median optical density. For the HD cohort, 98.8% were seropositive to the Wuhan strain, 97.6% against Delta and 100% against Omicron strains. For the PPP and AAP cohorts, 100% were seropositive against all 3 strains. Lastly, we examined the WHO NIBSC 20/136 standard and there was no loss of antibody binding to either VOC. Similarly, a dilution series of Sotrovimab (GSK) found this therapeutic monoclonal antibody bound similarly to all VOC. HighlightsO_LIIgG anti-SARS-CoV-2 Omicron spike glycoprotein antibody levels were high in 100% of health care workers (HCW), a general practice population considered clinically extremely vulnerable (CEV) and haemodialysis patients (HD) 4 weeks after a third SARS-CoV-2 vaccine dose (Pfizer-BioNtech-PFZ). C_LIO_LIFor both Delta and Omicron variant spike glycoproteins these antibody levels were highest in the CEV cohort who had previously received two doses of AstraZeneca ChAdOx1 nCoV-19 vaccine (AAP), lower in HCW who had previously received two doses of PFZ (PPP) and lowest in HD who had a mix of vaccines for the first and second dose C_LIO_LIPrior to this third vaccine dose and 6 months post second vaccine dose there was evidence of significant waning of antibodies against VOC. C_LI
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Texto completo: 1 Coleções: 09-preprints Base de dados: PREPRINT-MEDRXIV Tipo de estudo: Cohort_studies / Experimental_studies / Observational_studies / Prognostic_studies / Rct Idioma: En Ano de publicação: 2022 Tipo de documento: Preprint
Texto completo: 1 Coleções: 09-preprints Base de dados: PREPRINT-MEDRXIV Tipo de estudo: Cohort_studies / Experimental_studies / Observational_studies / Prognostic_studies / Rct Idioma: En Ano de publicação: 2022 Tipo de documento: Preprint
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