BSTP Review of 12 Case Studies Discussing the Challenges, Pathology, Immunogenicity, and Mechanisms of Inhaled Biologics

Author:

Hall A. Peter1ORCID,Tepper Jeffrey S.2,Boyle Molly H.3,Cary Maurice G.4,Flandre Thierry G.5ORCID,Piaia Alessandro5,Tarnow Inge6,Macri Nicholas P.2ORCID,Freke Mark C.7,Nikula Kristen J.8,Paul Graham R.9ORCID,Cauvin Annick10,Gregori Michela11,Haworth Richard9ORCID,Naylor Stuart12ORCID,Price Mark9,Robinson Ian N.13,Allen Andrew14,Gelzleichter Tom15,Hohlbaum Andreas M.16,Manetz Scott17,Wolfreys Alison1ORCID,Colman Karyn18ORCID,Fleurance Renaud10,Jones David19,Mukaratirwa Sydney11

Affiliation:

1. UCB BioPharma, Slough, United Kingdom

2. Tepper Nonclinical Consulting, San Carlos, CA, USA

3. Covance Inc., Somerset, NJ, USA

4. Pathology Experts GmbH, Witterswil, Switzerland

5. Novartis Institutes for Biomedical Research, Basel, Switzerland

6. Savara Pharmaceuticals, Hørsholm, Denmark

7. Charles River Laboratories Montreal ULC, Senneville, Quebec, Canada

8. Inotiv, Maryland Heights, MO, USA

9. GlaxoSmithKline, Ware, United Kingdom

10. UCB BioPharma SRL, Braine L’Alleud, Belgium

11. Covance, Huntingdon, United Kingdom

12. Charles River Laboratories, Edinburgh, United Kingdom

13. AstraZeneca, Melbourn, United Kingdom

14. Chiesi Farmaceutici S.p.A., Parma, Italy

15. Genentech Inc., South San Francisco, CA, USA

16. Sanofi, Zwijnaarde, Belgium

17. AstraZeneca, Gaithersburg, MD, USA

18. Genomics Institute for the Novartis Research Foundation, San Diego, CA, USA

19. MHRA, London, United Kingdom

Abstract

The inhalation route is a relatively novel drug delivery route for biotherapeutics and, as a result, there is a paucity of published data and experience within the toxicology/pathology community. In recent years, findings arising in toxicology studies with inhaled biologics have provoked concern and regulatory challenges due, in part, to the lack of understanding of the expected pathology, mechanisms, and adversity induced by this mode of delivery. In this manuscript, the authors describe 12 case studies, comprising 18 toxicology studies, using a range of inhaled biotherapeutics (monoclonal antibodies, fragment antigen-binding antibodies, domain antibodies, therapeutic proteins/peptides, and an oligonucleotide) in rodents, nonhuman primates (NHPs), and the rabbit in subacute (1 week) to chronic (26 weeks) toxicology studies. Analysis of the data revealed that many of these molecules were associated with a characteristic pattern of toxicity with high levels of immunogenicity. Microscopic changes in the airways consisted of a predominantly lymphoid perivascular/peribronchiolar (PV/PB) mononuclear inflammatory cell (MIC) infiltrate, whereas changes in the terminal airways/alveoli were characterized by simple (“uncomplicated”) increases in macrophages or inflammatory cell infiltrates ranging from mixed inflammatory cell infiltration to inflammation. The PV/PB MIC changes were considered most likely secondary to immunogenicity, whereas simple increases in alveolar macrophages were most likely secondary to clearance mechanisms. Alveolar inflammatory cell infiltrates and inflammation were likely induced by immune modulation or stimulation through pharmacologic effects on target biology or type III hypersensitivity (immune complex disease). Finally, a group of experts provide introductory thoughts regarding the adversity of inhaled biotherapeutics and the basis for reasonable differences of opinion that might arise between toxicologists, pathologists, and regulators.

Publisher

SAGE Publications

Subject

Cell Biology,Toxicology,Molecular Biology,Pathology and Forensic Medicine

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