Complex In Vitro Model Characterization for Context of Use in Toxicologic Pathology: Use Cases by Collaborative Teams of Biologists, Bioengineers, and Pathologists

Author:

Stokar-Regenscheit Nadine1,Bell Luisa1,Berridge Brian2,Rudmann Daniel3ORCID,Tagle Danilo4,Hargrove-Grimes Passley4,Schaudien Dirk5ORCID,Hahn Kerstin1,Kühnlenz Julia6,Ashton Randolph S.78,Tseng Min9ORCID,Reichelt Mike9,Laing Steven T.9,Kiyota Tomomi9,Chamanza Ronnie10ORCID,Sura Radhakrishna11,Tomlinson Lindsay12

Affiliation:

1. Roche Pharma Research and Early Development, Pharmaceutical Sciences, Roche Innovation Center Basel, F. Hoffmann-La Roche Ltd, Basel, Switzerland

2. B2 Pathology Solutions LLC, Cary, North Carolina, USA

3. Charles River Laboratories, Ashland, Ohio, USA

4. National Center for Advancing Translational Sciences/National Institutes of Health, Bethesda, Maryland, USA

5. Fraunhofer Institute for Toxicology and Experimental Medicine, Hannover, Germany

6. Bayer SAS, CropScience, Pathology & Mechanistic Toxicology, Sophia Antipolis, France

7. University of Wisconsin–Madison, Madison, Wisconsin, USA

8. Neurosetta LLC, Madison, Wisconsin, USA

9. Genentech, South San Francisco, California, USA

10. Johnson & Johnson Innovative Medicine, High Wycombe, UK

11. Gilead Sciences Inc., Foster City, California, USA

12. Pfizer Inc., Drug Safety Research and Development, Cambridge, Massachusetts, USA

Abstract

Complex in vitro models (CIVMs) offer the potential to increase the clinical relevance of preclinical efficacy and toxicity assessments and reduce the reliance on animals in drug development. The European Society of Toxicologic Pathology (ESTP) and Society for Toxicologic Pathology (STP) are collaborating to highlight the role of pathologists in the development and use of CIVM. Pathologists are trained in comparative animal medicine which enhances their understanding of mechanisms of human and animal diseases, thus allowing them to bridge between animal models and humans. This skill set is important for CIVM development, validation, and data interpretation. Ideally, diverse teams of scientists, including engineers, biologists, pathologists, and others, should collaboratively develop and characterize novel CIVM, and collectively assess their precise use cases (context of use). Implementing a morphological CIVM evaluation should be essential in this process. This requires robust histological technique workflows, image analysis techniques, and needs correlation with translational biomarkers. In this review, we demonstrate how such tissue technologies and analytics support the development and use of CIVM for drug efficacy and safety evaluations. We encourage the scientific community to explore similar options for their projects and to engage with health authorities on the use of CIVM in benefit-risk assessment.

Publisher

SAGE Publications

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