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IgG Seroconversion and Pathophysiology in Severe Acute Respiratory Syndrome Coronavirus 2 Infection.

Staines, HM; Kirwan, DE; Clark, DJ; Adams, ER; Augustin, Y; Byrne, RL; Cocozza, M; Cubas-Atienzar, AI; Cuevas, LE; Cusinato, M; et al. Staines, HM; Kirwan, DE; Clark, DJ; Adams, ER; Augustin, Y; Byrne, RL; Cocozza, M; Cubas-Atienzar, AI; Cuevas, LE; Cusinato, M; Davies, BMO; Davis, M; Davis, P; Duvoix, A; Eckersley, NM; Forton, D; Fraser, AJ; Garrod, G; Hadcocks, L; Hu, Q; Johnson, M; Kay, GA; Klekotko, K; Lewis, Z; Macallan, DC; Mensah-Kane, J; Menzies, S; Monahan, I; Moore, CM; Nebe-von-Caron, G; Owen, SI; Sainter, C; Sall, AA; Schouten, J; Williams, CT; Wilkins, J; Woolston, K; Fitchett, JRA; Krishna, S; Planche, T (2021) IgG Seroconversion and Pathophysiology in Severe Acute Respiratory Syndrome Coronavirus 2 Infection. Emerg Infect Dis, 27 (1). ISSN 1080-6059 https://doi.org/10.3201/eid2701.203074
SGUL Authors: Staines, Henry Michael Hu, Qinxue Krishna, Sanjeev Macallan, Derek Clive Planche, Timothy David Moore, Catherine Margaret Clark, David John Augustin, Yolanda Sydney Cusinato, Martina Elisa

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Abstract

We investigated the dynamics of seroconversion in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. During March 29–May 22, 2020, we collected serum samples and associated clinical data from 177 persons in London, UK, who had SARS-CoV-2 infection. We measured IgG against SARS-CoV-2 and compared antibody levels with patient outcomes, demographic information, and laboratory characteristics. We found that 2.0%–8.5% of persons did not seroconvert 3–6 weeks after infection. Persons who seroconverted were older, were more likely to have concurrent conditions, and had higher levels of inflammatory markers. Non-White persons had higher antibody concentrations than those who identified as White; these concentrations did not decline during follow-up. Serologic assay results correlated with disease outcome, race, and other risk factors for severe SARS-CoV-2 infection. Serologic assays can be used in surveillance to clarify the duration and protective nature of humoral responses to SARS-CoV-2 infection.

Item Type: Article
Additional Information: Staines HM, Kirwan DE, Clark DJ, Adams ER, Augustin Y, Byrne RL, et al. IgG Seroconversion and Pathophysiology in Severe Acute Respiratory Syndrome Coronavirus 2 Infection. Emerg Infect Dis. 2021;27(1):85-91. https://dx.doi.org/10.3201/eid2701.203074
Keywords: 2019 novel coronavirus disease, COVID-19, SARS-CoV-2, United Kingdom, antibodies, antibody responses, coronavirus, coronavirus disease, diagnostics, immunology, respiratory infections, serology, severe acute respiratory syndrome coronavirus 2, viruses, zoonoses, Adult, Aged, Antibodies, Viral, COVID-19, Enzyme-Linked Immunosorbent Assay, Female, Humans, Immunoglobulin G, Male, Middle Aged, Reverse Transcriptase Polymerase Chain Reaction, SARS-CoV-2, Seroconversion, Humans, Immunoglobulin G, Antibodies, Viral, Enzyme-Linked Immunosorbent Assay, Reverse Transcriptase Polymerase Chain Reaction, Adult, Aged, Middle Aged, Female, Male, Seroconversion, COVID-19, SARS-CoV-2, 1108 Medical Microbiology, 1117 Public Health and Health Services, 1103 Clinical Sciences, Microbiology
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: Emerg Infect Dis
ISSN: 1080-6059
Language: eng
Dates:
DateEvent
January 2021Published
30 November 2020Published Online
29 September 2020Accepted
Publisher License: Publisher's own licence
PubMed ID: 33256890
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/112670
Publisher's version: https://doi.org/10.3201/eid2701.203074

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