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Analysis of SARS-CoV-2 Antibodies in COVID-19 Convalescent Plasma using a Coronavirus Antigen Microarray
Rafael R de Assis; Aarti Jain; Rie Nakajima; Algis Jasinskas; Jiin Felgner; Joshua Miago Obiero; Oluwasanmi Oladapo Adenaiye; Sheldon Tai; Filbert H Hong; Philip Norris; Mars Stone; Graham Simmons; Anil Bagri; Martin Schreiber; Andreas Buser; Andreas Holbro; Manuel Battegay; Philip Hosimer; Charles Noesen; Donald K Milton; - Prometheus Study Group; Huw Davies; Paul Contestable; Laurence M Corash; Michael P Busch; Philip L Felgner; Saahir Khan.
Afiliação
  • Rafael R de Assis; University of California Irvine
  • Aarti Jain; University of California Irvine
  • Rie Nakajima; University of California Irvine
  • Algis Jasinskas; University of California Irvine
  • Jiin Felgner; University of California Irvine
  • Joshua Miago Obiero; University of California, Irvine
  • Oluwasanmi Oladapo Adenaiye; University of Maryland
  • Sheldon Tai; University of Maryland
  • Filbert H Hong; University of Maryland
  • Philip Norris; Vitalant Research Institute
  • Mars Stone; Vitalant Research Institute
  • Graham Simmons; Vitalant Research Institute
  • Anil Bagri; Cerus Corporation
  • Martin Schreiber; Oregon Health & Science University
  • Andreas Buser; University of Basel
  • Andreas Holbro; University of Basel
  • Manuel Battegay; University of Basel
  • Philip Hosimer; Ortho Clinical Diagnostics
  • Charles Noesen; Ortho Clinical Diagnostics
  • Donald K Milton; University of Maryland School of Public Health
  • - Prometheus Study Group; -
  • Huw Davies; University of California Irvine
  • Paul Contestable; Ortho Clinical Diagnostics
  • Laurence M Corash; Cerus Corporation
  • Michael P Busch; Vitalant Research Institute
  • Philip L Felgner; University of California Irvine
  • Saahir Khan; University of California Irvine
Preprint em Inglês | bioRxiv | ID: ppbiorxiv-043364
ABSTRACT
The current practice for diagnosis of COVID-19, based on SARS-CoV-2 PCR testing of pharyngeal or respiratory specimens in a symptomatic patient at high epidemiologic risk, likely underestimates the true prevalence of infection. Serologic methods can more accurately estimate the disease burden by detecting infections missed by the limited testing performed to date. Here, we describe the validation of a coronavirus antigen microarray containing immunologically significant antigens from SARS-CoV-2, in addition to SARS-CoV, MERS-CoV, common human coronavirus strains, and other common respiratory viruses. A comparison of antibody profiles detected on the array from control sera collected prior to the SARS-CoV-2 pandemic versus convalescent blood specimens from virologically confirmed COVID-19 cases demonstrates near complete discrimination of these two groups, with improved performance from use of antigen combinations that include both spike protein and nucleoprotein. This array can be used as a diagnostic tool, as an epidemiologic tool to more accurately estimate the disease burden of COVID-19, and as a research tool to correlate antibody responses with clinical outcomes.
Licença
cc_by_nd
Texto completo: Disponível Coleções: Preprints Base de dados: bioRxiv Tipo de estudo: Estudo diagnóstico / Experimental_studies / Estudo observacional / Estudo prognóstico / Rct Idioma: Inglês Ano de publicação: 2020 Tipo de documento: Preprint
Texto completo: Disponível Coleções: Preprints Base de dados: bioRxiv Tipo de estudo: Estudo diagnóstico / Experimental_studies / Estudo observacional / Estudo prognóstico / Rct Idioma: Inglês Ano de publicação: 2020 Tipo de documento: Preprint
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