TOP-Plus Is a Versatile Biosensor Platform for Monitoring SARS-CoV-2 Antibody Durability

Abstract Background Low initial severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antibody titers dropping to undetectable levels within months after infection have raised concerns about long-term immunity. Both the antibody levels and the avidity of the antibody–antigen interaction shoul...

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Veröffentlicht in:Clinical chemistry (Baltimore, Md.) Md.), 2021-09, Vol.67 (9), p.1249-1258
Hauptverfasser: Racine-Brzostek, Sabrina E, Karbaschi, Mohsen, Gaebler, Christian, Klasse, P J, Yee, Jim, Caskey, Marina, Yang, He S, Hao, Ying, Sukhu, Ashley, Rand, Sophie, Chadburn, Amy, Shi, Yuanyuan, Zuk, Robert, Nussenzweig, Michel C, Cushing, Melissa M, Zhao, Zhen
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Sprache:eng
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Zusammenfassung:Abstract Background Low initial severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antibody titers dropping to undetectable levels within months after infection have raised concerns about long-term immunity. Both the antibody levels and the avidity of the antibody–antigen interaction should be examined to understand the quality of the antibody response. Methods A testing-on-a-probe “plus” panel (TOP-Plus) was developed to include a newly developed avidity assay built into the previously described SARS-CoV-2 TOP assays that measured total antibody (TAb), surrogate neutralizing antibody (SNAb), IgM, and IgG on a versatile biosensor platform. TAb and SNAb levels were compared with avidity in previously infected individuals at 1.3 and 6.2 months after infection in paired samples from 80 patients with coronavirus disease 2019 (COVID-19). Sera from individuals vaccinated for SARS-CoV-2 were also evaluated for antibody avidity. Results The newly designed avidity assay in this TOP panel correlated well with a reference Bio-Layer Interferometry avidity assay (r = 0.88). The imprecision of the TOP avidity assay was
ISSN:0009-9147
1530-8561
DOI:10.1093/clinchem/hvab069