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

adversity alveolar macrophage antidrug antibody biopharmaceutical biotherapeutics bronchoalveolar lavage eosinophil immune complex disease immunogenicity inflammatory cell infiltrate inhaled biologics mouse particle primate pulmonary function rabbit rat

Journal

Toxicologic pathology
ISSN: 1533-1601
Titre abrégé: Toxicol Pathol
Pays: United States
ID NLM: 7905907

Informations de publication

Date de publication:
02 2021
Historique:
pubmed: 19 1 2021
medline: 31 7 2021
entrez: 18 1 2021
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 33455525
doi: 10.1177/0192623320976094
doi:

Substances chimiques

Biological Products 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

235-260

Auteurs

A Peter Hall (AP)

UCB BioPharma, Slough, United Kingdom.

Jeffrey S Tepper (JS)

Tepper Nonclinical Consulting, San Carlos, CA, USA.

Molly H Boyle (MH)

201915Covance Inc., Somerset, NJ, USA.

Maurice G Cary (MG)

Pathology Experts GmbH, Witterswil, Switzerland.

Thierry G Flandre (TG)

98560Novartis Institutes for Biomedical Research, Basel, Switzerland.

Alessandro Piaia (A)

98560Novartis Institutes for Biomedical Research, Basel, Switzerland.

Inge Tarnow (I)

Savara Pharmaceuticals, Hørsholm, Denmark.

Nicholas P Macri (NP)

Tepper Nonclinical Consulting, San Carlos, CA, USA.

Mark C Freke (MC)

70294Charles River Laboratories Montreal ULC, Senneville, Quebec, Canada.

Kristen J Nikula (KJ)

Inotiv, Maryland Heights, MO, USA.

Graham R Paul (GR)

1929GlaxoSmithKline, Ware, United Kingdom.

Annick Cauvin (A)

UCB BioPharma SRL, Braine L'Alleud, Belgium.

Michela Gregori (M)

Covance, Huntingdon, United Kingdom.

Richard Haworth (R)

1929GlaxoSmithKline, Ware, United Kingdom.

Stuart Naylor (S)

Charles River Laboratories, Edinburgh, United Kingdom.

Mark Price (M)

1929GlaxoSmithKline, Ware, United Kingdom.

Ian N Robinson (IN)

4625AstraZeneca, Melbourn, United Kingdom.

Andrew Allen (A)

18869Chiesi Farmaceutici S.p.A., Parma, Italy.

Tom Gelzleichter (T)

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

Andreas M Hohlbaum (AM)

Sanofi, Zwijnaarde, Belgium.

Scott Manetz (S)

AstraZeneca, Gaithersburg, MD, USA.

Alison Wolfreys (A)

UCB BioPharma, Slough, United Kingdom.

Karyn Colman (K)

70089Genomics Institute for the Novartis Research Foundation, San Diego, CA, USA.

Renaud Fleurance (R)

UCB BioPharma SRL, Braine L'Alleud, Belgium.

David Jones (D)

9059MHRA, London, United Kingdom.

Sydney Mukaratirwa (S)

Covance, Huntingdon, United Kingdom.

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Classifications MeSH