Neutralising antibodies to SARS coronavirus 2 in Scottish blood donors - a pilot study of the value of serology to determine population exposure

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Craig P Thompson

University of Oxford

Published 1 Project

Infectious Diseases

Nicholas Grayson

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Robert Paton

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Jai S. Bolton

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Jose Lourenco

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Bridget Penman

University of Warwick

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Lian Ni Lee

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Valerie Odon

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Juthathip Mongkolsapaya

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Senthil Chinnakannan

Published 2 Projects

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Wanwisa Dejnirattisai

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Matthew Edmans

University of Oxford

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Alexander Fyfe

University of Georgia

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Carol Imlach

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Kreepa Kooblall

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Nicholas Lim

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Chang Liu

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Cesar Lopez-Camacho

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Carol-Anne McInally

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Narayan Ramamurthy

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Immunology Infectious Diseases

Jeremy Ratcliff

Doctoral Student, University of Oxford

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Piyada Supasa

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Beibei Wang

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Alexander J Mentzer

Group Leader, Wellcome Centre for Human Genetics, University of Oxford

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Marc Turner

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Oliver L Sampson

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Calum Semple

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Epidemiology Infectious Diseases

J. Kenneth Baillie

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ISARIC4C Investigators

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Heli Harvala

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Gavin Screaton

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Nigel Temperton

Reader in Molecular Virology

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Paul Klenerman

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Lisa Jarvis

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Sunetra Gupta

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Peter Simmonds

University of Oxford

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Background. The progression and geographical distribution of SARS coronavirus 2 (SARS-CoV-2) infection in the UK and elsewhere is unknown because typically only symptomatic individuals are diagnosed. We performed a serological study of blood donors in Scotland between the 17th of March and the 18th of May to detect neutralising antibodies to SARS-CoV-2 as a marker of past infection and epidemic progression. Aim. To determine if sera from blood bank donors can be used to track the emergence and progression of the SARS-CoV-2 epidemic. Methods. A pseudotyped SARS-CoV-2 virus microneutralisation assay was used to detect neutralising antibodies to SARS-CoV-2. The study group comprised samples from 3,500 blood donors collected in Scotland between the 17th of March and 19th of May, 2020. Controls were collected from 100 donors in Scotland during 2019. Results. All samples collected on the 17th March, 2020 (n=500) were negative in the pseudotyped SARS-CoV-2 virus microneutralisation assay. Neutralising antibodies were detected in 6/500 donors from the 23th-26th of March. The number of samples containing neutralising antibodies did not significantly rise after the 5th-6th April until the end of the study on the 18th of May. We find that infections are concentrated in certain postcodes indicating that outbreaks of infection are extremely localised. In contrast, other areas remain comparatively untouched by the epidemic. Conclusion. These data indicate that sero-surveys of blood banks can serve as a useful tool for tracking the emergence and progression of an epidemic like the current SARS-CoV-2 outbreak.

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