Cargando…

A betacoronavirus multiplex microsphere immunoassay detects early SARS-CoV-2 seroconversion and antibody cross reactions

Sensitive and specific SARS-CoV-2 antibody assays remain critical for community and hospital-based SARS-CoV-2 surveillance. Here, we developed and applied a multiplex microsphere-based immunoassay (MMIA) for COVD-19 antibody studies that incorporates spike protein trimers of SARS-CoV-2, SARS-CoV-1,...

Descripción completa

Detalles Bibliográficos
Autores principales: Laing, Eric, Sterling, Spencer, Richard, Stephanie, Epsi, Nusrat, Phogat, Shreshta, Samuels, Emily, Yan, Lianying, Moreno, Nicole, Coles, Christian, Drew, Matthew, Mehalko, Jennifer, English, Caroline, Merritt, Scott, Mende, Katrin, Chung, Kevin, Clifton, G., Munster, Vincent, de Wit, Emmie, Tribble, David, Agan, Brian, Esposito, Dominic, Lanteri, Charlotte, Mitre, Edward, Burgess, Timothy, Broder, Chritopher
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Journal Experts 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7709164/
https://www.ncbi.nlm.nih.gov/pubmed/33269345
http://dx.doi.org/10.21203/rs.3.rs-105768/v1
Descripción
Sumario:Sensitive and specific SARS-CoV-2 antibody assays remain critical for community and hospital-based SARS-CoV-2 surveillance. Here, we developed and applied a multiplex microsphere-based immunoassay (MMIA) for COVD-19 antibody studies that incorporates spike protein trimers of SARS-CoV-2, SARS-CoV-1, MERS-CoV, and the seasonal human betacoronaviruses, HCoV-HKU1 and HCoV-OC43, that enables measurement of off-target pre-existing cross-reactive antibodies. The MMIA performances characteristics are: 98% sensitive and 100% specific for human subject samples collected as early as 10 days from symptom onset. The MMIA permitted the simultaneous identification of SARS-CoV-2 seroconversion and the induction of SARS-CoV-2 IgG antibody cross reactions to SARS-CoV-1 and MERS-CoV. Further, synchronous increases of HCoV-OC43 IgG antibody levels was detected with SARS-CoV-2 seroconversion in a subset of subjects for whom early infection sera were available prior to their SARS-CoV-2 seroconversion, suggestive of an HCoV-OC43 memory response triggered by SARS-CoV-2 infection.