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ABSTRACT: Introduction
Early in the COVID-19 pandemic, reagent availability was not uniform, and infrastructure had to be urgently adapted to undertake COVID-19 surveillance.Methods
Before the validation of centralized testing, two enzyme-linked immunosorbent assays (ELISA) were established independently at two decentralized sites using different reagents and instrumentation. We compared the results of these assays to assess the longitudinal humoral response of SARS-CoV-2-positive (i.e., PCR-confirmed), non-hospitalized individuals with mild to moderate symptoms, who had contracted SARSCoV-2 prior to the appearance of variants of concern in Québec, Canada.Results
The two assays exhibited a high degree of concordance to identify seropositive individuals, thus validating the robustness of the methods. The results also confirmed that serum immunoglobulins persist ≥ 6 months post-infection among non-hospitalized adults and that the antibodies elicited by infection cross-reacted with the antigens from P.1 (Gamma) and B.1.617.2 (Delta) variants of concern.Discussion
Together, these results demonstrate that immune surveillance assays can be rapidly and reliably established when centralized testing is not available or not yet validated, allowing for robust immune surveillance.
SUBMITTER: Djaileb A
PROVIDER: S-EPMC9895839 | biostudies-literature | 2022
REPOSITORIES: biostudies-literature
Djaïleb Abdelhadi A Lavallée Étienne É Parker Megan-Faye MF Cayer Marie-Pierre MP Desautels Florence F de Grandmont Marie Joëlle MJ Stuible Matthew M Gervais Christian C Durocher Yves Y Trottier Sylvie S Boudreau Denis D Masson Jean-Francois JF Brouard Danny D Pelletier Joelle N JN
Frontiers in immunology 20230120
<h4>Introduction</h4>Early in the COVID-19 pandemic, reagent availability was not uniform, and infrastructure had to be urgently adapted to undertake COVID-19 surveillance.<h4>Methods</h4>Before the validation of centralized testing, two enzyme-linked immunosorbent assays (ELISA) were established independently at two decentralized sites using different reagents and instrumentation. We compared the results of these assays to assess the longitudinal humoral response of SARS-CoV-2-positive (i.e., P ...[more]