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. 2020 Dec 8;27(5):789.e1-789.e5.
doi: 10.1016/j.cmi.2020.11.025. Online ahead of print.

Detection of SARS-CoV-2 N-antigen in blood during acute COVID-19 provides a sensitive new marker and new testing alternatives

Collaborators, Affiliations

Detection of SARS-CoV-2 N-antigen in blood during acute COVID-19 provides a sensitive new marker and new testing alternatives

Quentin LE Hingrat et al. Clin Microbiol Infect. .

Erratum in

Abstract

Objectives: Molecular assays on nasopharyngeal swabs remain the cornerstone of COVID-19 diagnostic. The high technicalities of nasopharyngeal sampling and molecular assays, as well as scarce resources of reagents, limit our testing capabilities. Several strategies failed, to date, to fully alleviate this testing process (e.g. saliva sampling or antigen testing on nasopharyngeal samples). We assessed the clinical performances of SARS-CoV-2 nucleocapsid antigen (N-antigen) ELISA detection in serum or plasma using the COVID-19 Quantigene® (AAZ, France) assay.

Methods: Performances were determined on 63 sera from 63 non-COVID patients and 227 serum samples (165 patients) from the French COVID and CoV-CONTACT cohorts with RT-PCR confirmed SARS-CoV-2 infection, including 142 serum (114 patients) obtained within 14 days after symptoms' onset.

Results: Specificity was 98.4% (95% confidence interval [CI], 95.3 to 100). Sensitivity was 79.3% overall (180/227, 95% CI, 74.0 to 84.6) and 93.0% (132/142, 95% CI, 88.7 to 97.2) within 14 days after symptoms onset. 91 included patients had a sera and nasopharyngeal swabs collected in the same 24 hours. Among those with high nasopharyngeal viral loads, i.e. Ct value below 30 and 33, only 1/50 and 4/67 tested negative for N-antigenemia, respectively. Among those with a negative nasopharyngeal RT-PCR, 8/12 presented positive N-antigenemia; the lower respiratory tract was explored for 6 of these 8 patients, showing positive RT-PCR in 5 cases.

Conclusion: This is the first evaluation of a commercially available serum N-antigen detection assay. It presents a robust specificity and sensitivity within the first 14 days after symptoms onset. This approach provides a valuable new option for COVID-19 diagnosis, only requiring a blood draw and easily scalable in all clinical laboratories.

Keywords: Antigen; Antigenemia; Blood; COVID-19; Diagnostic; Plasma; SARS-CoV-2; Serum.

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Figures

Fig. 1
Fig. 1
(A) Evolution of N-antigen sera levels in SARS-CoV-2-infected patients according to hospitalization status (n = 227 serum samples from 165 patients); sequential samples are connected with a grey line, while the positivity threshold value for N-antigen (2.97 pg/mL) is indicated with a dashed red line. (B) N-antigenaemia levels according to delay since symptoms onset. (C) N-antigen sera levels according to positive and negative RNAaemia status (n = 146 sera, n = 89 patients). (D) N-antigen sera levels according to E-gene cycle threshold value of 104 nasopharyngeal swabs collected within 24 hr (n = 91 patients).

References

    1. Rao M., Rashid F.A., Sabri F.S.A.H., Jamil N.N., Zain R., Hashim R. Comparing nasopharyngeal swab and early morning saliva for the identification of SARS-CoV-2. Clin Infect Dis. 2020 doi: 10.1093/cid/ciaa1156. - DOI - PMC - PubMed
    1. Wyllie A.L., Fournier J., Casanovas-Massana A., Campbell M., Tokuyama M., Vijayakumar P. Saliva or nasopharyngeal swab specimens for detection of SARS-CoV-2. N Engl J Med. 2020;383:1283–1286. doi: 10.1056/NEJMc2016359. - DOI - PMC - PubMed
    1. Flower B., Brown J.C., Simmons B., Moshe M., Frise R., Penn R. Clinical and laboratory evaluation of SARS-CoV-2 lateral flow assays for use in a national COVID-19 seroprevalence survey. Thorax. 2020;75:1082–1088. doi: 10.1136/thoraxjnl-2020-215732. - DOI - PMC - PubMed
    1. Dinnes J., Deeks J.J., Adriano A., Berhane S., Davenport C., Dittrich S. Rapid, point-of-care antigen and molecular-based tests for diagnosis of SARS-CoV-2 infection. Cochrane Database Syst Rev. 2020 doi: 10.1002/14651858.CD013705. - DOI - PMC - PubMed
    1. Ogata A.F., Maley A.M., Wu C., Gilboa T., Norman M., Lazarovits R. Ultra-sensitive serial profiling of SARS-CoV-2 antigens and antibodies in plasma to understand disease progression in COVID-19 patients with severe disease. Clin Chem. 2020;66:1562–1572. doi: 10.1093/clinchem/hvaa213. - DOI - PMC - PubMed