Magenta Therapeutics, Cambridge, Massachusetts, USA.
Biogen, Cambridge, Massachusetts, USA.
Toxicol Pathol. 2023 Jul;51(5):278-305. doi: 10.1177/01926233231213851.
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.
背根神经节(DRG)、三叉神经节(TG)、其他感觉神经节和自主神经节可能会受到某些受试物类别的损伤,包括抗肿瘤化学疗法、腺相关病毒为基础的基因疗法、反义寡核苷酸、神经生长因子抑制剂和氨基糖苷类抗生素。本文综述了在评估此类受试物(TA)的产品安全性中常用的常见非临床物种中的神经节解剖、细胞学和病理学(强调感觉神经节)。与感觉神经节损伤相关的主要组织病理学发现包括神经元变性、坏死和/或丧失;卫星胶质细胞和/或施万细胞数量增加;白细胞浸润和/或炎症。次级神经纤维变性和/或神经胶质反应可能发生在神经、背根脊神经、脊髓(背侧和偶尔侧束),有时还发生在脑干。与 TA 给药相关的神经节发现可能是由于 TA 暴露和/或与直接向中枢神经系统或神经节输送 TA 相关的创伤所致。在某些情况下,需要将 TA 相关的影响与一系列人为和/或自发的背景变化区分开来。