PLoS ONE (Jan 2021)

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,
  • Patrick Schuetz

DOI
https://doi.org/10.1371/journal.pone.0259731
Journal volume & issue
Vol. 16, no. 11
p. e0259731

Abstract

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BackgroundPlasma-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 methodsData 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.ResultsWe 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.ConclusionThe work presented in this paper may have important implications for physicians and patients who use Privigen for indicated diseases.