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Abstract

Aim: Preexisting anti-polyethylene glycol (PEG) antibodies (APAs) may affect the efficacy and safety of PEGylated compounds. Omontys® and Krystexxa® withdrawal and SARS-CoV-2 RNA vaccine anaphylaxis have all been linked to APAs. This project aimed to develop and validate a method to detect total antibodies against PEG, pre- and post-dose. Materials & methods: The repetitive, linear PEG structure prevented the use of a bridging homogenous format, hence the requirement to use a solid-phase extraction and acid dissociation assay coupled with the Meso Scale Discovery® platform. Results & conclusion: Using singlicate analysis, the method was validated to successfully detect APA pre- and post-dose, with a crucial aspect of the method being the preparation of an appropriate negative control.

Keywords:

  • anti-PEG magnitude/quantification/titer
  • anti-PEG screening and confirmatory
  • individual screening
  • PEGylated therapeutics
  • pre- and post-dose anti-PEG antibodies
  • preexisting anti-PEG antibodies
  • preexisting antibody purification
  • SARS-CoV-2 RNA vaccine anti-PEG antibodies
  • singlicate assessment in immunogenicity
  • solid-phase extraction and acid dissociation
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