Department of Physical Therapy, University of Florida, Gainesville, FL, USA.
McKnight Brain Institute, University of Florida, Gainesville, FL, USA.
Gene Ther. 2021 Aug;28(7-8):402-412. doi: 10.1038/s41434-021-00225-1. Epub 2021 Feb 11.
Dysfunction and/or reduced activity in the tongue muscles contributes to conditions such as dysphagia, dysarthria, and sleep disordered breathing. Current treatments are often inadequate, and the tongue is a readily accessible target for therapeutic gene delivery. In this regard, gene therapy specifically targeting the tongue motor system offers two general strategies for treating lingual disorders. First, correcting tongue myofiber and/or hypoglossal (XII) motoneuron pathology in genetic neuromuscular disorders may be readily achieved by intralingual delivery of viral vectors. The retrograde movement of viral vectors such as adeno-associated virus (AAV) enables targeted distribution to XII motoneurons via intralingual viral delivery. Second, conditions with impaired or reduced tongue muscle activation can potentially be treated using viral-driven chemo- or optogenetic approaches to activate or inhibit XII motoneurons and/or tongue myofibers. Further considerations that are highly relevant to lingual gene therapy include (1) the diversity of the motoneurons which control the tongue, (2) the patterns of XII nerve branching, and (3) the complexity of tongue muscle anatomy and biomechanics. Preclinical studies show considerable promise for lingual directed gene therapy in neuromuscular disease, but the potential of such approaches is largely untapped.
舌肌无力或活动障碍可导致吞咽困难、构音障碍和睡眠呼吸障碍等疾病。目前的治疗方法往往效果不佳,而舌头是治疗基因传递的一个易于接近的靶点。在这方面,专门针对舌运动系统的基因治疗为治疗舌部疾病提供了两种一般策略。首先,通过舌内递送病毒载体,可轻易实现针对遗传性神经肌肉疾病中舌肌纤维和/或舌下神经(XII)运动神经元病变的矫正。腺相关病毒(AAV)等病毒载体的逆行运动,使通过舌内病毒递送来靶向分布至 XII 运动神经元成为可能。其次,对于存在舌肌无力或活动减少的情况,可以通过病毒驱动的化学遗传学或光遗传学方法来激活或抑制 XII 运动神经元和/或舌肌纤维,从而进行潜在的治疗。与舌基因治疗高度相关的进一步考虑因素包括:(1)控制舌头的运动神经元的多样性;(2)XII 神经分支的模式;(3)舌肌解剖结构和生物力学的复杂性。临床前研究显示,舌定向基因治疗在神经肌肉疾病方面具有相当大的应用前景,但这些方法的潜力尚未得到充分发掘。