Selecting COVID ‐19 convalescent plasma for neutralizing antibody potency using a high‐capacity SARS‐CoV ‐2 antibody assay
Year: 2021
Type: article
Abstract: BACKGROUND Efficacy of COVID-19 convalescent plasma (CCP) to treat COVID-19 is hypothesized to be associated with the concentration of neutralizing antibodies (nAb) to SARS-CoV-2. High capacity serologic assays detecting binding antibodies (bAb) have been developed, nAb assays are not adaptable to high-throughput testing. We sought to determine the effectiveness of using surrogate bAb signal-to-cutoff ratios (S/CO) in predicting nAb titers using a pseudovirus reporter viral particle neutralization (RVPN) assay. METHODS CCP donor serum collected by 3 US blood collectors was tested with a bAb assay (Ortho Clinical Diagnostics VITROS Anti-SARS-CoV-2 Total, CoV2T) and a nAb RVPN assay. CoV2T prediction effectiveness at S/CO thresholds was evaluated for RVPN nAb NT 50 titers using receiver operating characteristic analysis. RESULTS 753 CCPs were tested with median CoV2T S/CO of 71.2 and median NT 50 of 527.5. Proportions of CCP donors with NT 50 over various target nAb titers were 86% ≥1:80, 76% ≥1:160, and 62%≥1:320. Increasing CoV2Ts reduced the sensitivity to predict NT 50 titers, while specificity to identify those below thresholds increased. As the targeted NT 50 increased, the positive predictive value fell with reciprocal increase in negative predictive value. S/CO thresholds were thus less able to predict target NT 50 titers. CONCLUSION Selection of a clinically effective nAb titer will impact availability of CCP. Product release with CoV2T assay S/CO thresholds must balance the risk of releasing products below target nAb titers with the cost of false negatives. A two-step testing scheme may be optimal, with nAb testing on CoV2T samples with S/COs below thresholds.
Source: Transfusion
DOI: 10.1111/trf.16321
Institutions: Nationwide Children's Hospital, American Red Cross, Vitalant Research Institute, University of California, San Francisco, OneBlood, Ortho Clinical Diagnostics (United States), University of New Mexico, Vitalant, Vitalant, Vanderbilt University, Dartmouth College, University of Colorado Anschutz, University of Colorado Denver
Language: English
Subfield: Infectious Diseases
Field: Medicine
Domain: Health Sciences
Open Access status: bronze
OpenAlex ID: W3126821514
