Modelling the concentration of anti-SARS-CoV-2 immunoglobulin G in intravenous immunoglobulin product batches
Sara Stinca,
Thomas W Barnes,
Peter Vogel,
Wilfried Meyers,
Johannes Schulte-Pelkum,
Daniel Filchtinski,
Laura Steller,
Thomas Hauser,
Sandro Manni,
David F Gardiner,
Sharon Popik,
Nathan J Roth and
Patrick Schuetz
PLOS ONE, 2021, vol. 16, issue 11, 1-11
Abstract:
Background: Plasma-derived intravenous immunoglobulin (IVIg) products contain a dynamic spectrum of immunoglobulin (Ig) G reactivities reflective of the donor population from which they are derived. We sought to model the concentration of anti-severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) IgG which could be expected in future plasma pool and final-product batches of CSL Behring’s immunoglobulin product Privigen. Study design and methods: Data was extracted from accessible databases, including the incidence of coronavirus disease 2019 and SARS-CoV-2 vaccination status, antibody titre in convalescent and vaccinated groups and antibody half-life. Together, these parameters were used to create an integrated mathematical model that could be used to predict anti-SARS-CoV-2 antibody levels in future IVIg preparations. Results: We predict that anti-SARS-CoV-2 IgG concentration will peak in batches produced in mid-October 2021, containing levels in the vicinity of 190-fold that of the mean convalescent (unvaccinated) plasma concentration. An elevated concentration (approximately 35-fold convalescent plasma) is anticipated to be retained in batches produced well into 2022. Measurement of several Privigen batches using the Phadia™ EliA™ SARS-CoV-2-Sp1 IgG binding assay confirmed the early phase of this model. Conclusion: The work presented in this paper may have important implications for physicians and patients who use Privigen for indicated diseases.
Date: 2021
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Persistent link: https://EconPapers.repec.org/RePEc:plo:pone00:0259731
DOI: 10.1371/journal.pone.0259731
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