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Evaluation and deployment of isotype-specific salivary antibody assays for detecting previous SARS-CoV-2 infection in children and adults.
Thomas, Amy C; Oliver, Elizabeth; Baum, Holly E; Gupta, Kapil; Shelley, Kathryn L; Long, Anna E; Jones, Hayley E; Smith, Joyce; Hitchings, Benjamin; di Bartolo, Natalie; Vasileiou, Kate; Rabi, Fruzsina; Alamir, Hanin; Eghleilib, Malak; Francis, Ore; Oliver, Jennifer; Morales-Aza, Begonia; Obst, Ulrike; Shattock, Debbie; Barr, Rachael; Collingwood, Lucy; Duale, Kaltun; Grace, Niall; Livera, Guillaume Gonnage; Bishop, Lindsay; Downing, Harriet; Rodrigues, Fernanda; Timpson, Nicholas; Relton, Caroline L; Toye, Ashley; Woolfson, Derek N; Berger, Imre; Goenka, Anu; Davidson, Andrew D; Gillespie, Kathleen M; Williams, Alistair J K; Bailey, Mick; Brooks-Pollock, Ellen; Finn, Adam; Halliday, Alice.
  • Thomas AC; Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK. amyc.thomas@bristol.ac.uk.
  • Oliver E; Bristol Vaccine Centre, School of Cellular and Molecular Medicine, University of Bristol, Bristol, UK. amyc.thomas@bristol.ac.uk.
  • Baum HE; Bristol Vaccine Centre, School of Cellular and Molecular Medicine, University of Bristol, Bristol, UK.
  • Gupta K; Bristol Vaccine Centre, School of Cellular and Molecular Medicine, University of Bristol, Bristol, UK.
  • Shelley KL; School of Biochemistry, University of Bristol, Bristol, UK.
  • Long AE; BrisSynBio, University of Bristol, Bristol, UK.
  • Jones HE; Imophoron Ltd, Science Creates, Old Market, Midland Road, Bristol, UK.
  • Smith J; School of Biochemistry, University of Bristol, Bristol, UK.
  • Hitchings B; BrisSynBio, University of Bristol, Bristol, UK.
  • di Bartolo N; School of Chemistry, University of Bristol, Bristol, UK.
  • Vasileiou K; Translational Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
  • Rabi F; Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
  • Alamir H; Bristol Vaccine Centre, School of Cellular and Molecular Medicine, University of Bristol, Bristol, UK.
  • Eghleilib M; Bristol Vaccine Centre, School of Cellular and Molecular Medicine, University of Bristol, Bristol, UK.
  • Francis O; School of Biochemistry, University of Bristol, Bristol, UK.
  • Oliver J; NIHR Blood and Transplant Research Unit in Red Cell Products, University of Bristol, Bristol, UK.
  • Morales-Aza B; School of Biochemistry, University of Bristol, Bristol, UK.
  • Obst U; School of Biochemistry, University of Bristol, Bristol, UK.
  • Shattock D; Bristol Vaccine Centre, School of Cellular and Molecular Medicine, University of Bristol, Bristol, UK.
  • Barr R; Bristol Vaccine Centre, School of Cellular and Molecular Medicine, University of Bristol, Bristol, UK.
  • Collingwood L; Bristol Veterinary School, University of Bristol, Bristol, UK.
  • Duale K; Bristol Vaccine Centre, Population Health Sciences, University of Bristol, Bristol, UK.
  • Grace N; Bristol Vaccine Centre, School of Cellular and Molecular Medicine, University of Bristol, Bristol, UK.
  • Livera GG; School of Cellular and Molecular Medicine, University of Bristol, Bristol, UK.
  • Bishop L; Bristol Bioresource Laboratories, Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
  • Downing H; Bristol Vaccine Centre, School of Cellular and Molecular Medicine, University of Bristol, Bristol, UK.
  • Rodrigues F; Bristol Royal Hospital for Children, University Hospitals Bristol and Weston NHS Foundation Trust, Upper Maudlin Street, Bristol, BS2 8BJ, UK.
  • Timpson N; Bristol Vaccine Centre, Population Health Sciences, University of Bristol, Bristol, UK.
  • Relton CL; Bristol Vaccine Centre, School of Cellular and Molecular Medicine, University of Bristol, Bristol, UK.
  • Toye A; Bristol Vaccine Centre, Population Health Sciences, University of Bristol, Bristol, UK.
  • Woolfson DN; Bristol Vaccine Centre, Population Health Sciences, University of Bristol, Bristol, UK.
  • Berger I; Bristol Vaccine Centre, Population Health Sciences, University of Bristol, Bristol, UK.
  • Goenka A; NIHR Bristol Biomedical Research Centre, University of Bristol, Bristol, UK.
  • Davidson AD; Hospital Pediátrico, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal.
  • Gillespie KM; Faculdade de Medicina, Universidade de Coimbra, Coimbra, Portugal.
  • Williams AJK; Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
  • Bailey M; MRC Integrative Epidemiology Unit, Population Health Sciences, Bristol Medical School, Bristol, UK.
  • Brooks-Pollock E; MRC Integrative Epidemiology Unit, Population Health Sciences, Bristol Medical School, Bristol, UK.
  • Finn A; School of Biochemistry, University of Bristol, Bristol, UK.
  • Halliday A; NIHR Blood and Transplant Research Unit in Red Cell Products, University of Bristol, Bristol, UK.
Commun Med (Lond) ; 3(1): 37, 2023 Mar 15.
Article in English | MEDLINE | ID: covidwho-2284009
ABSTRACT

BACKGROUND:

Saliva is easily obtainable non-invasively and potentially suitable for detecting both current and previous SARS-CoV-2 infection, but there is limited evidence on the utility of salivary antibody testing for community surveillance.

METHODS:

We established 6 ELISAs detecting IgA and IgG antibodies to whole SARS-CoV-2 spike protein, to its receptor binding domain region and to nucleocapsid protein in saliva. We evaluated diagnostic performance, and using paired saliva and serum samples, correlated mucosal and systemic antibody responses. The best-performing assays were field-tested in 20 household outbreaks.

RESULTS:

We demonstrate in test accuracy (N = 320), spike IgG (ROC AUC 95.0%, 92.8-97.3%) and spike IgA (ROC AUC 89.9%, 86.5-93.2%) assays to discriminate best between pre-pandemic and post COVID-19 saliva samples. Specificity was 100% in younger age groups (0-19 years) for spike IgA and IgG. However, sensitivity was low for the best-performing assay (spike IgG 50.6%, 39.8-61.4%). Using machine learning, diagnostic performance was improved when a combination of tests was used. As expected, salivary IgA was poorly correlated with serum, indicating an oral mucosal response whereas salivary IgG responses were predictive of those in serum. When deployed to household outbreaks, antibody responses were heterogeneous but remained a reliable indicator of recent infection. Intriguingly, unvaccinated children without confirmed infection showed evidence of exposure almost exclusively through specific IgA responses.

CONCLUSIONS:

Through robust standardisation, evaluation and field-testing, this work provides a platform for further studies investigating SARS-CoV-2 transmission and mucosal immunity with the potential for expanding salivo-surveillance to other respiratory infections in hard-to-reach settings.
If a person has been previously infected with SARS-CoV-2 they will produce specific proteins, called antibodies. These are present in the saliva and blood. Saliva is easier to obtain than blood, so we developed and evaluated six tests that detect SARS-CoV-2 antibodies in saliva in children and adults. Some tests detected antibodies to a particular protein made by SARS-CoV-2 called the spike protein, and these tests worked best. The most accurate results were obtained by using a combination of tests. Similar tests could also be developed to detect other respiratory infections which will enable easier identification of infected individuals.

Full text: Available Collection: International databases Database: MEDLINE Type of study: Diagnostic study / Experimental Studies / Prognostic study / Randomized controlled trials Topics: Long Covid Language: English Journal: Commun Med (Lond) Year: 2023 Document Type: Article Affiliation country: S43856-023-00264-2

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Diagnostic study / Experimental Studies / Prognostic study / Randomized controlled trials Topics: Long Covid Language: English Journal: Commun Med (Lond) Year: 2023 Document Type: Article Affiliation country: S43856-023-00264-2