Modelling the concentration of anti-SARS-CoV-2 immunoglobulin G in intravenous immunoglobulin product batches

PLoS One. 2021 Nov 29;16(11):e0259731. doi: 10.1371/journal.pone.0259731. eCollection 2021.

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antibodies, Viral / analysis*
  • Antibodies, Viral / blood
  • COVID-19 / blood
  • COVID-19 / immunology*
  • Humans
  • Immunoglobulin G / analysis*
  • Immunoglobulins, Intravenous / analysis*
  • Middle Aged
  • Models, Biological*
  • SARS-CoV-2 / physiology*
  • Tissue Donors
  • Young Adult

Substances

  • Antibodies, Viral
  • Immunoglobulin G
  • Immunoglobulins, Intravenous

Grants and funding

Funding for this work was provided by CSL Behring AG and Thermo Fisher Scientific ImmunoDiagnostics Phadia GmbH. Editorial assistance was funded by CSL Behring.