| Literature DB >> 23954437 |
Theo Rispens1, Margreet H Hart, Pleuni Ooijevaar-de Heer, Astrid van Leeuwen, Anke Vennegoor, Joep Killestein, Gerrit-Jan Wolbink, Desiree van der Kleij.
Abstract
Direct comparison of immunogenicity data is hampered by differential drug interference in different assay formats. In this paper we identify a drug-related factor that influences the extent of drug interference. We systematically investigated the influence of drug valency of different antibody-derived biologicals on the drug interference, using mono- and bivalent formats of adalimumab as a model system. Our results indicate that compared to regular bivalent antibodies, antibody-derived drugs that are monovalent result in less drug interference. Two real-life examples were examined: natalizumab, an IgG4 antibody that becomes effectively monovalent in vivo due to Fab arm exchange, and certolizumab pegol, a pegylated Fab fragment. For both drugs it was demonstrated that drug interference is less pronounced in an antigen-binding test compared to similar assays for other therapeutic antibodies. When comparing immunogenicity data obtained for different biologicals this phenomenon should be taken into account.Entities:
Keywords: ABT; ADA; Anti-drug antibody (ADA); Bispecific antibody; Certolizumab; Drug interference; GSH; Natalizumab; anti-drug antibody; antigen binding test; reduced glutathione
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Year: 2013 PMID: 23954437 DOI: 10.1016/j.jpba.2013.07.022
Source DB: PubMed Journal: J Pharm Biomed Anal ISSN: 0731-7085 Impact factor: 3.935