Cai Charlene W, Grey Josh A, Hubmacher Dirk, Han Woojin M
Department of Orthopaedics, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Department of Biology, The College of New Jersey, Ewing, New Jersey, USA.
Adv Wound Care (New Rochelle). 2025 Mar;14(3):159-175. doi: 10.1089/wound.2024.0079. Epub 2024 Jul 10.
Volumetric muscle loss (VML) is caused by the loss of significant amounts of skeletal muscle tissue. VML cannot be repaired by intrinsic regenerative processes, resulting in permanent loss of muscle function and disability. Current rehabilitative-focused treatment strategies lack efficacy and do not restore muscle function, indicating the need for the development of effective regenerative strategies. Recent developments implicate biomaterial-based approaches for promoting muscle repair and functional restoration post-VML. Specifically, bioscaffolds transplanted in the injury site have been utilized to mimic endogenous cues of the ablated tissue to promote myogenic pathways, increase neo-myofiber synthesis, and ultimately restore contractile function to the injured unit. Despite the development and preclinical testing of various biomaterial-based regenerative strategies, effective therapies for patients are not available. The unique challenges posed for biomaterial-based treatments of VML injuries, including its scalability and clinical applicability beyond small-animal models, impede progress. Furthermore, production of tissue-engineered constructs is technically demanding, with reproducibility issues at scale and complexities in achieving vascularization and innervation of large constructs. Biomaterial-based regenerative strategies designed to comprehensively address the pathophysiology of VML are needed. Considerations for clinical translation, including scalability and regulatory compliance, should also be considered when developing such strategies. In addition, an integrated approach that combines regenerative and rehabilitative strategies is essential for ensuring functional improvement.
容积性肌肉损失(VML)是由大量骨骼肌组织的丧失引起的。VML无法通过内在的再生过程修复,导致肌肉功能永久丧失和残疾。目前以康复为重点的治疗策略缺乏疗效,无法恢复肌肉功能,这表明需要开发有效的再生策略。最近的进展表明,基于生物材料的方法可促进VML后的肌肉修复和功能恢复。具体而言,移植到损伤部位的生物支架已被用于模拟被切除组织的内源性信号,以促进肌源性途径,增加新肌纤维的合成,并最终恢复受损单元的收缩功能。尽管已经开发并进行了各种基于生物材料的再生策略的临床前测试,但尚未有针对患者的有效疗法。VML损伤基于生物材料的治疗所面临的独特挑战,包括其可扩展性以及超越小动物模型的临床适用性,阻碍了进展。此外,组织工程构建体的生产技术要求很高,存在规模上的可重复性问题以及实现大型构建体血管化和神经支配的复杂性。需要设计出能够全面解决VML病理生理学问题的基于生物材料的再生策略。在制定此类策略时,还应考虑临床转化的因素,包括可扩展性和法规合规性。此外,将再生策略和康复策略相结合的综合方法对于确保功能改善至关重要。