Standardizing terms, definitions and concepts for describing and interpreting unwanted immunogenicity of biopharmaceuticals: recommendations of the Innovative Medicines Initiative ABIRISK consortium

Author:

,Rup B1,Pallardy M2,Sikkema D3,Albert T4,Allez M5,Broet P6,Carini C7,Creeke P8,Davidson J9,De Vries N10,Finco D11,Fogdell-Hahn A12,Havrdova E13,Hincelin-Mery A14,Holland M C15,Jensen P E H16,Jury E C17,Kirby H18,Kramer D19,Lacroix-Desmazes S20,Legrand J21,Maggi E22,Maillère B23,Mariette X24,Mauri C25,Mikol V26,Mulleman D27,Oldenburg J4,Paintaud G28,Pedersen C R29,Ruperto N30,Seitz R31,Spindeldreher S32,Deisenhammer F33

Affiliation:

1. Pfizer, Immunogenicity Sciences Disciple, Pharmacokinetics, Dynamics and Metabolism

2. INSERM, UMR996, Faculté Pharmacie, Université Paris Sud, France

3. GlaxoSmithKline, Clinical Immunology–Biopharm, King of Prussia, PA, USA

4. Institute of Experimental Haematology and Transfusion Medicine, University Clinic Bonn, Bonn, Germany

5. Hôpital Saint-Louis, Department of Gastroenterology, GETAID, Paris, France

6. INSERM, UMR669, University of Paris Sud, France

7. Pfizer, Early Biotech Clinical Development, Cambridge, MA, USA

8. Centre for Neuroscience and Trauma, Blizard Institute, Queen Mary University of London, London, UK

9. GlaxoSmithKline, Worldwide Epidemiology, Southall, UK

10. Clinical Immunology and Rheumatology, University of Amsterdam, Amsterdam, the Netherlands

11. Pfizer, Drug Safety R&D, Groton, CT, USA

12. Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden

13. Department of Neurology and Center for Clinical Neuroscience, MS Center, Charles University in Prague, Prague, Czech Republic

14. Sanofi-Aventis, Clinical Exploratory and Pharmacology, Chilly-Mazerin, FR

15. GlaxoSmithKline, Clinical Immunology–Biopharm R&D, King of Prussia, PA, USA

16. Department of Neurology, University of Copenhagen, Copenhagen, Denmark

17. Centre for Rheumatology, University College London, London, UK

18. UCB Pharma, Bioanalytical R&D, Slough, UK

19. Merck-Serono, Institute of Drug Metabolism and Pharmacokinetics, Grafing, Germany

20. INSERM, UMR S 1138, Université Pierre et Marie Curie, Paris, France

21. Ipsen Innovation, Pharmacokinetics Drug Metabolism Department, Les Ulis, France

22. Dipartimento di Medicina Sperimentale e Clinica, Universita di Firenze, Firenze, Italy

23. CEA-Saclay Institute of Biology and Technologies, Gif sur Yvette, France

24. INSERM, U1012, Hôpitaux Universitaires Paris Sud, Rhumatologie, Paris, France

25. Centre for Rheumatology Research, University College London, London, UK

26. Sanofi Aventis, Structural Biology, Paris, France

27. University of Tours Francois Rabelais, CNRS UMR 7292, Tours, France

28. CNRS UMR 7292 ‘GICC’, Faculty of Medicine, Tours, France

29. Novo Nordisk, Immunogenicity, Måløv, Denmark

30. Istituto Giannina Gaslini, Pediatria II, Rheumatology, Genova, Italy

31. Division of Haematology/Transfusion Medicine, Paul-Ehrlich-Institut, Langen, Germany

32. Drug Metabolism Pharmacokinetics-Biologics, Novartis Institutes for Biomedical Research, Basel, Switzerland

33. Department of Neurology, Innsbruck Medical University, Innsbruck, Austria

Abstract

Summary Biopharmaceuticals (BPs) represent a rapidly growing class of approved and investigational drug therapies that is contributing significantly to advancing treatment in multiple disease areas, including inflammatory and autoimmune diseases, genetic deficiencies and cancer. Unfortunately, unwanted immunogenic responses to BPs, in particular those affecting clinical safety or efficacy, remain among the most common negative effects associated with this important class of drugs. To manage and reduce risk of unwanted immunogenicity, diverse communities of clinicians, pharmaceutical industry and academic scientists are involved in: interpretation and management of clinical and biological outcomes of BP immunogenicity, improvement of methods for describing, predicting and mitigating immunogenicity risk and elucidation of underlying causes. Collaboration and alignment of efforts across these communities is made difficult due to lack of agreement on concepts, practices and standardized terms and definitions related to immunogenicity. The Innovative Medicines Initiative (IMI; www.imi-europe.org), ABIRISK consortium [Anti-Biopharmaceutical (BP) Immunization Prediction and Clinical Relevance to Reduce the Risk; www.abirisk.eu] was formed by leading clinicians, academic scientists and EFPIA (European Federation of Pharmaceutical Industries and Associations) members to elucidate underlying causes, improve methods for immunogenicity prediction and mitigation and establish common definitions around terms and concepts related to immunogenicity. These efforts are expected to facilitate broader collaborations and lead to new guidelines for managing immunogenicity. To support alignment, an overview of concepts behind the set of key terms and definitions adopted to date by ABIRISK is provided herein along with a link to access and download the ABIRISK terms and definitions and provide comments (http://www.abirisk.eu/index_t_and_d.asp).

Funder

European Union's Seventh Framework Programme

European Federation of Pharmaceutical Industries and Associations

Publisher

Oxford University Press (OUP)

Subject

Immunology,Immunology and Allergy

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