IgG Seroconversion and Pathophysiology in Severe Acute Respiratory Syndrome Coronavirus 2 Infection
Supporting Files
Public Domain
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November 30 2020
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File Language:
English
Details
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Alternative Title:Emerg Infect Dis
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Personal Author:Staines, Henry M. ; Kirwan, Daniela E. ; Clark, David J. ; Adams, Emily R. ; Augustin, Yolanda ; Byrne, Rachel L. ; Cocozza, Michael ; Cubas-Atienzar, Ana I. ; Cuevas, Luis E. ; Cusinato, Martina ; Davies, Benedict M.O. ; Davis, Mark ; Davis, Paul ; Duvoix, Annelyse ; Eckersley, Nicholas M. ; Forton, Daniel ; Fraser, Alice J. ; Garrod, Gala ; Hadcocks, Linda ; Hu, Qinxue ; Johnson, Michael ; Kay, Grant A. ; Klekotko, Kesja ; Lewis, Zawditu ; Macallan, Derek C. ; Mensah-Kane, Josephine ; Menzies, Stefanie ; Monahan, Irene ; Moore, Catherine M. ; Nebe-von-Caron, Gerhard ; Owen, Sophie I. ; Sainter, Chris ; Sall, Amadou A. ; Schouten, James ; Williams, Christopher T. ; Wilkins, John ; Woolston, Kevin ; Fitchett, Joseph R.A. ; Krishna, Sanjeev ; Planche, Tim
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Description: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.
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Subjects:
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Source:Emerg Infect Dis. 27(1):85-91
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Pubmed ID:33256890
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Pubmed Central ID:PMC7774532
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Document Type:
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Volume:27
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Issue:1
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Collection(s):
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Main Document Checksum:urn:sha256:bae8de3f99715280f53f6e54925826f92c0c6a02cdde9ac5dc5c73302e9cb358
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Download URL:
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File Type:
Supporting Files
File Language:
English
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Emerging Infectious Diseases