Assessing Vulnerability to COVID-19 in High-Risk Populations: The Role of SARS-CoV-2 Spike-Targeted Serology.

COVID-19 SARS-CoV-2 antibody immunocompromised severe acute respiratory syndrome coronavirus 2 vaccination

Journal

Population health management
ISSN: 1942-7905
Titre abrégé: Popul Health Manag
Pays: United States
ID NLM: 101481266

Informations de publication

Date de publication:
02 2023
Historique:
entrez: 17 2 2023
pubmed: 18 2 2023
medline: 22 2 2023
Statut: ppublish

Résumé

Individuals at increased risk for severe coronavirus disease-2019 (COVID-19) outcomes, due to compromised immunity or other risk factors, would benefit from objective measures of vulnerability to infection based on vaccination or prior infection. The authors reviewed published data to identify a specific role and interpretation of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) spike-targeted serology testing. Specific recommendations are provided for an evidence-based and clinically-useful interpretation of SARS-CoV-2 spike-targeted serology to identify vulnerability to infection and potential subsequent adverse outcomes. Decreased vaccine effectiveness among immunocompromised individuals is linked to correspondingly high rates of breakthrough infections. Negative results on SARS-CoV-2 antibody tests are associated with increased risk for subsequent infection. "Low-positive" results on semiquantitative SARS-CoV-2 spike-targeted antibody tests may help identify persons at increased risk as well. Standardized SARS-CoV-2 spike-targeted antibody tests may provide objective information on the risk of SARS-CoV-2 infection and associated adverse outcomes. This holds especially for high-risk populations that demonstrate a relatively high rate of seronegativity. The widespread availability of such tests presents an opportunity to refine risk assessment for individuals with suboptimal SARS-CoV-2 antibody levels and to promote effective interventions. Interim federal guidance would support physicians and patients while additional investigations are pursued.

Identifiants

pubmed: 36799932
doi: 10.1089/pop.2022.0241
doi:

Substances chimiques

Antibodies, Viral 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

29-36

Auteurs

Harvey W Kaufman (HW)

Quest Diagnostics, Secaucus, New Jersey, USA.

William A Meyer (WA)

Quest Diagnostics, Secaucus, New Jersey, USA.

Nigel J Clarke (NJ)

Quest Diagnostics, Secaucus, New Jersey, USA.

Jeff Radcliff (J)

Quest Diagnostics, Secaucus, New Jersey, USA.

Christopher M Rank (CM)

Roche Diagnostics GmbH, Penzberg, Germany.

James Freeman (J)

Siemens Healthineers, Tarrytown, New York, USA.

Marcia Eisenberg (M)

LabCorp, Burlington, North Carolina, USA.

Laura Gillim (L)

LabCorp, Burlington, North Carolina, USA.

William G Morice (WG)

Mayo Medical Laboratories, Rochester, Minnesota, USA.

David M Briscoe (DM)

Boston Children's Hospital, Boston, Massachusetts, USA.

David S Perlin (DS)

Center for Discovery and Innovation, Hackensack Meridian Health, Nutley, New Jersey, USA.

Jay G Wohlgemuth (JG)

Quest Diagnostics, Secaucus, New Jersey, USA.

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Classifications MeSH