Selected article for: "assay specificity and cov protein"

Author: Rodriguez-Moncayo, Roberto; Cedillo-Alcantar, Diana F; Guevara-Pantoja, Pablo E; Chavez-Pineda, Oriana G; Hernandez-Ortiz, Jose A; Amador-Hernandez, Josue U; Rojas-Velasco, Gustavo; Sanchez-Muñoz, Fausto; Manzur-Sandoval, Daniel; Patino-Lopez, Luis D; May-Arrioja, Daniel A; Posadas-Sanchez, Rosalinda; Vargas-Alarcon, Gilberto; Garcia-Cordero, Jose L
Title: A high-throughput multiplexed microfluidic device for COVID-19 serology assays.
  • Cord-id: 60sixa0q
  • Document date: 2020_12_15
  • ID: 60sixa0q
    Snippet: The applications of serology tests to the virus SARS-CoV-2 are diverse, ranging from diagnosing COVID-19, understanding the humoral response to this disease, and estimating its prevalence in a population, to modeling the course of the pandemic. COVID-19 serology assays will significantly benefit from sensitive and reliable technologies that can process dozens of samples in parallel, thus reducing costs and time; however, they will also benefit from biosensors that can assess antibody reactivitie
    Document: The applications of serology tests to the virus SARS-CoV-2 are diverse, ranging from diagnosing COVID-19, understanding the humoral response to this disease, and estimating its prevalence in a population, to modeling the course of the pandemic. COVID-19 serology assays will significantly benefit from sensitive and reliable technologies that can process dozens of samples in parallel, thus reducing costs and time; however, they will also benefit from biosensors that can assess antibody reactivities to multiple SARS-CoV-2 antigens. Here, we report a high-throughput microfluidic device that can assess antibody reactivities against four SARS-CoV-2 antigens from up to 50 serum samples in parallel. This semi-automatic platform measures IgG and IgM levels against four SARS-CoV-2 proteins: the spike protein (S), the S1 subunit (S1), the receptor-binding domain (RBD), and the nucleocapsid (N). After assay optimization, we evaluated sera from infected individuals with COVID-19 and a cohort of archival samples from 2018. The assay achieved a sensitivity of 95% and a specificity of 91%. Nonetheless, both parameters increased to 100% when evaluating sera from individuals in the third week after symptom onset. To further assess our platform's utility, we monitored the antibody titers from 5 COVID-19 patients over a time course of several weeks. Our platform can aid in global efforts to control and understand COVID-19.

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