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Performance of SARS COV-2 IgG Anti-N As an Independent Marker of Exposure to SARS COV-2 in an Unvaccinated West African Population

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Specialty Tropical Medicine
Date 2023 Aug 14
PMID 37580023
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Abstract

Determination of previous SARS-COV-2 infection is hampered by the absence of a standardized test. The marker used to assess previous exposure is IgG antibody to the nucleocapsid (IgG anti-N), although it is known to wane quickly from peripheral blood. The accuracies of seven antibody tests (virus neutralization test, IgG anti-N, IgG anti-spike [anti-S], IgG anti-receptor binding domain [anti-RBD], IgG anti-N + anti-RBD, IgG anti-N + anti-S, and IgG anti-S + anti-RBD), either singly or in combination, were evaluated on 502 cryopreserved serum samples collected before the COVID-19 vaccination rollout in Kumasi, Ghana. The accuracy of each index test was measured using a composite reference standard based on a combination of neutralization test and IgG anti-N antibody tests. According to the composite reference, 262 participants were previously exposed; the most sensitive test was the virus neutralization test, with 95.4% sensitivity (95% CI: 93.6-97.3), followed by 79.0% for IgG anti-N + anti-S (95% CI: 76.3-83.3). The most specific tests were virus neutralization and IgG anti-N, both with 100% specificity. Viral neutralization and IgG anti-N + anti-S were the overall most accurate tests, with specificity/sensitivity of 100/95.2% and 79.0/92.1%, respectively. Our findings indicate that IgG anti-N alone is an inadequate marker of prior exposure to SARS COV-2 in this population. Virus neutralization assay appears to be the most accurate assay in discerning prior infection. A combination of IgG anti-N and IgG anti-S is also accurate and suited for assessment of SARS COV-2 exposure in low-resource settings.

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References
1.
Robbiani D, Gaebler C, Muecksch F, Lorenzi J, Wang Z, Cho A . Convergent antibody responses to SARS-CoV-2 in convalescent individuals. Nature. 2020; 584(7821):437-442. PMC: 7442695. DOI: 10.1038/s41586-020-2456-9. View

2.
Van Elslande J, Gruwier L, Godderis L, Vermeersch P . Estimated Half-Life of SARS-CoV-2 Anti-Spike Antibodies More Than Double the Half-Life of Anti-nucleocapsid Antibodies in Healthcare Workers. Clin Infect Dis. 2021; 73(12):2366-2368. PMC: 7989510. DOI: 10.1093/cid/ciab219. View

3.
Marzo R, Sami W, Alam M, Acharya S, Jermsittiparsert K, Songwathana K . Hesitancy in COVID-19 vaccine uptake and its associated factors among the general adult population: a cross-sectional study in six Southeast Asian countries. Trop Med Health. 2022; 50(1):4. PMC: 8727234. DOI: 10.1186/s41182-021-00393-1. View

4.
Wiecek W, Ahuja A, Chaudhuri E, Kremer M, Simoes Gomes A, Snyder C . Testing fractional doses of COVID-19 vaccines. Proc Natl Acad Sci U S A. 2022; 119(8). PMC: 8872706. DOI: 10.1073/pnas.2116932119. View

5.
Gallais F, Gantner P, Bruel T, Velay A, Planas D, Wendling M . Evolution of antibody responses up to 13 months after SARS-CoV-2 infection and risk of reinfection. EBioMedicine. 2021; 71:103561. PMC: 8390300. DOI: 10.1016/j.ebiom.2021.103561. View