Scientific and Regulatory Policy Committee Technical Review: Biology and Pathology of Ganglia in Animal Species Used for Nonclinical Safety Testing

Author:

Bennet Bindu M.1ORCID,Pardo Ingrid D.2,Assaf Basel T.3ORCID,Buza Elizabeth4ORCID,Cramer Sarah D.5,Crawford LaTasha K.6ORCID,Engelhardt Jeffery A.7,Galbreath Elizabeth J.8ORCID,Grubor Branka2ORCID,Morrison James P.9ORCID,Osborne Tanasa S.10,Sharma Alok K.11,Bolon Brad12ORCID

Affiliation:

1. Magenta Therapeutics, Cambridge, Massachusetts, USA

2. Biogen, Cambridge, Massachusetts, USA

3. Sanofi, Cambridge, Massachusetts, USA

4. University of Pennsylvania, Philadelphia, Pennsylvania, USA

5. StageBio, Frederick, Maryland, USA

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

7. Ionis Pharmaceuticals, Carlsbad, California, USA

8. Independent Consultant, Lexington, Massachusetts, USA

9. Charles River Laboratories, Inc., Shrewsbury, Massachusetts, USA

10. Novartis Pharmaceuticals, East Hanover, New Jersey, USA

11. Labcorp Drug Development, Madison, Wisconsin, USA

12. GEMpath Inc., Longmont, Colorado, USA

Abstract

Dorsal root ganglia (DRG), trigeminal ganglia (TG), other sensory ganglia, and autonomic ganglia may be injured by some test article classes, including anti-neoplastic chemotherapeutics, adeno-associated virus-based gene therapies, antisense oligonucleotides, nerve growth factor inhibitors, and aminoglycoside antibiotics. This article reviews ganglion anatomy, cytology, and pathology (emphasizing sensory ganglia) among common nonclinical species used in assessing product safety for such test articles (TAs). Principal histopathologic findings associated with sensory ganglion injury include neuron degeneration, necrosis, and/or loss; increased satellite glial cell and/or Schwann cell numbers; and leukocyte infiltration and/or inflammation. Secondary nerve fiber degeneration and/or glial reactions may occur in nerves, dorsal spinal nerve roots, spinal cord (dorsal and occasionally lateral funiculi), and sometimes the brainstem. Ganglion findings related to TA administration may result from TA exposure and/or trauma related to direct TA delivery into the central nervous system or ganglia. In some cases, TA-related effects may need to be differentiated from a spectrum of artifactual and/or spontaneous background changes.

Publisher

SAGE Publications

Subject

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

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