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Impaired systemic nucleocapsid antigen clearance in severe COVID-19.
Bauer, Christian; Mack, Elisabeth; Hefter, Véronique; Fischer, Alexandra; Volland, Kirsten; Skevaki, Chrysanthi; Neubauer, Andreas; Gress, Thomas; Becker, Stephan; Keller, Christian.
Afiliación
  • Bauer C; Department of Gastroenterology, Endocrinology, Metabolism and Infectiology, University Hospital Marburg, Philipps University, Marburg, Germany.
  • Mack E; Department of Internal Medicine, Hematology and Oncology, University Hospital Marburg, Philipps University, Marburg, Germany.
  • Hefter V; Institute of Virology, University Hospital Marburg, Philipps University, Marburg, Germany.
  • Fischer A; Institute of Virology, University Hospital Marburg, Philipps University, Marburg, Germany.
  • Volland K; Institute of Virology, University Hospital Marburg, Philipps University, Marburg, Germany.
  • Skevaki C; Universities of Giessen and Marburg Lung Center (UGMLC), Philipps University Marburg, German Center for Lung Research (DZL) Marburg, Institute of Laboratory Medicine, Marburg, Germany.
  • Neubauer A; Department of Internal Medicine, Hematology and Oncology, University Hospital Marburg, Philipps University, Marburg, Germany.
  • Gress T; Department of Gastroenterology, Endocrinology, Metabolism and Infectiology, University Hospital Marburg, Philipps University, Marburg, Germany.
  • Becker S; Institute of Virology, University Hospital Marburg, Philipps University, Marburg, Germany.
  • Keller C; Institute of Virology, University Hospital Marburg, Philipps University, Marburg, Germany.
J Med Virol ; 95(8): e29032, 2023 08.
Article en En | MEDLINE | ID: mdl-37581876
ABSTRACT
The circulating nucleocapsid (NCP) antigen of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is detectable in coronavirus disease-2019 (COVID-19) patients. To better understand the biology of disease severity, we investigated NCP clearance kinetics in hospitalized COVID-19 patients. Serum NCP was quantified using a commercial NCP-specific enzyme-linked immunoassay in hospitalized COVID-19 patients (n = 63) during their hospital stay. Results were correlated to COVID-19 disease severity, inflammation parameters, antibody response, and results of SARS-CoV-2 PCR from nasopharyngeal swabs. We demonstrate that NCP antigen levels in serum remained elevated in 21/45 (46.7%) samples from patients in intensive care units (ICU) after >8 days postdiagnosis. The proportion of ICU patients with detectable antigenemia declined only gradually from 84.6% to 25.0% over several weeks. This was in contrast to complete NCP clearance in all non-ICU patients after 8 days, and also in contrast to mucosal clearance of the virus as measured by PCR. Antigen clearance was associated with higher IgG against S1 but not NCP. Clearance of NCP antigenemia is delayed in >40% of severely ill COVID-19 patients. Thus, NCP antigenemia detected after 8 days post COVID-19 diagnosis is a characteristic of patients requiring intensive care. Prospective trials should further investigate NCP antigen clearance kinetics as a mechanistic biomarker.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: COVID-19 Tipo de estudio: Diagnostic_studies / Observational_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: J Med Virol Año: 2023 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: COVID-19 Tipo de estudio: Diagnostic_studies / Observational_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: J Med Virol Año: 2023 Tipo del documento: Article País de afiliación: Alemania