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Towards Internationally standardised humoral Immune Correlates of Protection from SARS CoV 2 infection and COVID-19 disease
Javier Castillo-Olivares; David Wells; Matteo Ferrari; Andrew Chan; Peter Smith; Angalee Nadesalingam; Minna Paloniemi; George Carnell; Luis Ohlendorf; Diego Cantoni; Martin Mayora-Neto; Phillip Palmer; Paul Tonks; Nigel Temperton; Patrick Neckermann; David Peterhoff; Ralf James Wagner; Rainer Doffinger; Sarah Kempster; Ashley Otter; Amanda Semper; Tim Brooks; Mark Page; Anna Albecka; John Briggs; Leo James; Wilhelm Schwabble; Dr HE Baxendale; Jonathan Heeney.
Afiliação
  • Javier Castillo-Olivares; University of Cambridge
  • David Wells; University of Cambridge; DIOSynVax
  • Matteo Ferrari; University of Cambridge; DioSynvax
  • Andrew Chan; University of Cambridge
  • Peter Smith; University of Cambridge
  • Angalee Nadesalingam; University of Cambridge
  • Minna Paloniemi; University of Cambridge; Fimlab Laboratories, Tampere, Finland
  • George Carnell; University of Cambridge
  • Luis Ohlendorf; University of Cambridge
  • Diego Cantoni; University of Kent
  • Martin Mayora-Neto; University of Kent
  • Phillip Palmer; University of Cambridge
  • Paul Tonks; University of Cambridge
  • Nigel Temperton; University of Kent
  • Patrick Neckermann; University of Regensburg
  • David Peterhoff; University of Regensburg, Germany
  • Ralf James Wagner; Institute of Medical Microbiology and Hygiene
  • Rainer Doffinger; Addenbrooke's Hospital, Cambridge, UK
  • Sarah Kempster; National Institute for Biological Standards and Control, UK
  • Ashley Otter; National Infection Service, Public Health England, Porton Down, UK
  • Amanda Semper; National Infection Service, Public Health England, Porton Down, UK
  • Tim Brooks; National Infection Service, Public Health England, Porton Down, UK
  • Mark Page; National Institute for Biological Standards and Control
  • Anna Albecka; MRC Laboratory of Molecular Biology, Cambridge, UK
  • John Briggs; MRC Laboratory of Molecular Biology, Cambridge, UK
  • Leo James; MRC Laboratory of Molecular Biology, Cambridge, UK
  • Wilhelm Schwabble; Complement Laboratory, Department of Veterinary Medicine, University of Cambridge, UK
  • Dr HE Baxendale; Royal Papworth Hospital NHS Foundation Trust
  • Jonathan Heeney; University of Cambridge, UK
Preprint em En | PREPRINT-MEDRXIV | ID: ppmedrxiv-21257572
ABSTRACT
Precision monitoring of antibody responses during the COVID-19 pandemic is increasingly important during large scale vaccine rollout and rise in prevalence of Severe Acute Respiratory Syndrome-related Coronavirus-2 (SARS-CoV-2) variants of concern (VOC). Equally important is defining Correlates of Protection (CoP) for SARS-CoV-2 infection and COVID-19 disease. Data from epidemiological studies and vaccine trials identified virus neutralising antibodies (Nab) and SARS-CoV-2 antigen-specific (notably RBD, and S) binding antibodies as candidate CoP. In this study, we used the World Health Organisation (WHO) international standard to benchmark neutralising antibody responses and a large panel of binding antibody assays to compare convalescent sera obtained from a) COVID-19 patients; b) SARS-CoV-2 seropositive healthcare workers (HCW) and c) seronegative HCW. The ultimate aim of this study, was to identify biomarkers of humoral immunity that could be used as candidate CoP in internationally accepted unitage. Whenever suitable, the antibody levels of the samples studied were expressed in International Units (INU) for virus neutralisation assays or International Binding Antibody Units (BAU) for ELISA tests. In this work we used commercial and non-commercial antibody binding assays; a lateral flow test for detection of SARS-CoV-2-specific IgG / IgM; a high throughput multiplexed particle flow cytometry assay for SARS-CoV-2 Spike (S), Nucleocapsid (N) and Receptor Binding Domain (RBD) proteins); a multiplex antigen semi-automated immuno-blotting assay measuring IgM, IgA and IgG; a pseudotyped microneutralisation test (pMN) and electroporation-dependent neutralisation assay (EDNA). Our results indicate that overall, severe COVID-19 patients showed statistically significantly higher levels of SARS-CoV-2-specific neutralising antibodies (average 1029 IU/ml) than those observed in seropositive HCW with mild or asymptomatic infections (379 IU/ml) and that clinical severity scoring, based on WHO guidelines was tightly correlated with neutralisation and RBD / S binding assays. In addition, there was a positive correlation between severity, N-antibody assays and intracellular virus neutralisation.
Licença
cc_by_nc_nd
Texto completo: 1 Coleções: 09-preprints Base de dados: PREPRINT-MEDRXIV Tipo de estudo: Observational_studies / Prognostic_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Preprint
Texto completo: 1 Coleções: 09-preprints Base de dados: PREPRINT-MEDRXIV Tipo de estudo: Observational_studies / Prognostic_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Preprint