UCL School of Pharmacy, University College London, London, UK; UCL Centre for Nerve Engineering, London, UK.
UCL School of Pharmacy, University College London, London, UK; UCL Centre for Nerve Engineering, London, UK; Glialign Ltd, UCL School of Pharmacy, London, UK.
Acta Biomater. 2021 Nov;135:203-213. doi: 10.1016/j.actbio.2021.08.030. Epub 2021 Aug 26.
A surgical autograft remains the clinical gold-standard therapy for gap repair following peripheral nerve injury, however, challenges remain with achieving full recovery and reducing donor-site morbidity. Engineered Neural Tissue (EngNT) manufactured using differentiated CTX0E03 human stem cells (EngNT-CTX) has been developed as a potential 'off the shelf' allogeneic autograft replacement. Ensheathed within a collagen membrane developed to facilitate biomechanical integration, EngNT-CTX was used to bridge a critical-length (15 mm) sciatic nerve gap injury in athymic nude rats. The effectiveness of EngNT-CTX was compared to an autograft using outcome measures that assessed neuronal regeneration and functional recovery at 8 and 16 weeks. At both time points EngNT-CTX restored electrophysiological nerve conduction and functional reinnervation of downstream muscles to the same extent as the autograft. Histological analysis confirmed that more motor neurons had successfully regenerated through the repair in EngNT-CTX in comparison to the autograft at 8 weeks, which was consistent with the electrophysiology, with the number of motor neurons similar in both groups by 16 weeks. The total number of neurons (motor + sensory) was greater in autografts than EngNT-CTX at 8 weeks, indicating that more sensory fibres may have sprouted in those animals at this time point. In conclusion, this study provides evidence to support the effectiveness of EngNT-CTX as a replacement for the nerve autograft, as the functional regeneration assessed through histological and electrophysiological outcome measures demonstrated equivalent performance. STATEMENT OF SIGNIFICANCE: Following injury a peripheral nerve has the capacity to regenerate naturally, however, in the case of severe damage where there is a gap the current gold-standard microsurgical intervention is an autograft. This is associated with serious limitations including tissue availability and donor-site morbidity. Tissue engineering aims to overcome these limitations by building a construct from therapeutic cells and biomaterials as a means to mimic and replace the autograft. In this study engineered neural tissue (EngNT) was manufactured using human stem cells (CTX) to bridge a critical-length gap injury. When compared to the autograft in an animal model the EngNT-CTX construct restored function to an equivalent or greater extent.
外科自体移植物仍然是周围神经损伤后间隙修复的临床金标准治疗方法,然而,在实现完全恢复和减少供体部位发病率方面仍然存在挑战。使用分化的 CTX0E03 人干细胞制造的工程化神经组织(EngNT-CTX)已被开发为潜在的“现成的”同种异体自体移植物替代品。EngNT-CTX 被包裹在一种胶原蛋白膜中,该膜旨在促进生物力学整合,用于桥接 15mm 长的坐骨神经间隙损伤的免疫缺陷裸鼠。使用评估神经再生和 8 周和 16 周时功能恢复的结局测量指标,比较了 EngNT-CTX 与自体移植物的效果。在这两个时间点,EngNT-CTX 恢复了电生理神经传导,并使下游肌肉的功能再神经支配恢复到与自体移植物相同的程度。组织学分析证实,与自体移植物相比,在 8 周时,更多的运动神经元通过修复成功再生到 EngNT-CTX 中,这与电生理学一致,到 16 周时,两组的运动神经元数量相似。在 8 周时,自体移植物中的神经元(运动神经元+感觉神经元)总数多于 EngNT-CTX,表明此时更多的感觉纤维可能在这些动物中发芽。总之,这项研究提供了证据支持 EngNT-CTX 作为神经自体移植物替代品的有效性,因为通过组织学和电生理结局测量评估的功能再生表现出等效性能。研究意义:受伤后,周围神经有自然再生的能力,然而,在严重损伤导致间隙的情况下,当前的金标准显微外科干预是自体移植物。这与严重的局限性相关,包括组织可用性和供体部位发病率。组织工程旨在通过使用治疗细胞和生物材料构建构建体来克服这些局限性,作为模拟和替代自体移植物的手段。在这项研究中,使用人干细胞(CTX)制造了工程化神经组织(EngNT),以桥接临界长度间隙损伤。在动物模型中,与自体移植物相比,EngNT-CTX 构建体恢复功能的程度相等或更高。