AI Article Synopsis

  • Certain test articles, like chemotherapy drugs and gene therapies, can injure different types of sensory and autonomic ganglia, including dorsal root and trigeminal ganglia.
  • The article reviews the anatomy and pathology of these ganglia in common nonclinical species used for product safety evaluation, focusing on changes in neuron health and glial cell activity following injury.
  • Key findings from ganglion injury include neuron degeneration, increased glial cells and inflammation, with potential secondary effects extending to nearby nerves and the spinal cord, necessitating differentiation from natural background changes.

Article 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.

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Source
http://dx.doi.org/10.1177/01926233231213851DOI Listing

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