Tan S H S, Wong J R Y, Sim S J Y, Tjio C K E, Wong K L, Chew J R J, Hui J H P, Toh W S
Department of Orthopaedic Surgery, National University Health System, Singapore.
Department of Orthopaedic Surgery, Sengkang General Hospital, Singhealth, Singapore.
Mater Today Bio. 2020 Jun 27;7:100067. doi: 10.1016/j.mtbio.2020.100067. eCollection 2020 Jun.
The ability of bone for regeneration has long been recognized. However, once beyond a critical size, spontaneous regeneration of bone is limited. Several studies have focused on enhancing bone regeneration by applying mesenchymal stromal/stem cells (MSCs) in the treatment strategies. Despite the therapeutic efficacy of MSCs in bone regeneration, cell-based therapies are impeded by several challenges in maintaining the optimal cell potency and viability during expansion, storage, and final delivery to patients. Recently, there has been a paradigm shift in therapeutic mechanism of MSCs in tissue repair from one based on cellular differentiation and replacement to one based on secretion and paracrine signaling. Among the broad spectrum of trophic factors, extracellular vesicles particularly the exosomes have been reported to be therapeutically efficacious in several injury/disease indications, including bone defects and diseases. The current systematic review aims to summarize the results of the existing animal studies which were conducted to evaluate the therapeutic efficacy of MSC exosomes for bone regeneration. Following the Preferred Reporting Items for Systematic Reviews and Meta-analysis guidelines, the PubMed and The Cochrane Library database were searched for relevant controlled preclinical animal studies. A total of 23 studies were identified, with the total sample size being 690 rats or mice and 38 rabbits. Generally, MSC exosomes were found to be efficacious for bone regeneration in animal models of bone defects and diseases such as osteonecrosis and osteoporosis. In these studies, MSC exosomes promoted new bone formation with supporting vasculature and displayed improved morphological, biomechanical, and histological outcomes, coupled with positive effects on cell survival, proliferation, and migration, osteogenesis, and angiogenesis. Unclear-to-low risk in bias and incomplete reporting in the primary studies highlighted the need for standardization in outcome measurements and reporting. Further studies in large animal models to establish the safety and efficacy would provide useful information on guiding the design of clinical trials.
骨骼的再生能力早已得到认可。然而,一旦超过临界大小,骨骼的自发再生就会受到限制。多项研究聚焦于在治疗策略中应用间充质基质/干细胞(MSCs)来促进骨再生。尽管MSCs在骨再生方面具有治疗效果,但基于细胞的疗法在扩增、储存以及最终输送给患者的过程中,面临着维持最佳细胞效力和活力的诸多挑战。最近,MSCs在组织修复中的治疗机制发生了范式转变,从基于细胞分化和替代转变为基于分泌和旁分泌信号传导。在众多营养因子中,细胞外囊泡,尤其是外泌体,已被报道在包括骨缺损和疾病在内的多种损伤/疾病适应症中具有治疗效果。本系统综述旨在总结现有动物研究的结果,这些研究旨在评估MSC外泌体对骨再生的治疗效果。按照系统评价和荟萃分析的首选报告项目指南,在PubMed和Cochrane图书馆数据库中搜索相关的对照临床前动物研究。共识别出23项研究,总样本量为690只大鼠或小鼠以及38只兔子。总体而言,在骨缺损和诸如骨坏死和骨质疏松症等疾病的动物模型中,发现MSC外泌体对骨再生有效。在这些研究中,MSC外泌体促进了带有支持血管的新骨形成,并显示出改善的形态学、生物力学和组织学结果,同时对细胞存活、增殖和迁移、成骨和血管生成具有积极影响。主要研究中存在的偏倚风险不明确至低以及报告不完整,凸显了结果测量和报告标准化的必要性。在大型动物模型中进行进一步研究以确定安全性和有效性,将为指导临床试验设计提供有用信息。