Pileyre Baptiste, Gandolfi Silvia, Abad Catalina, Jaworski Thara, Drouot Laurent, Jean Laetitia, Boyer Olivier, Dubus Isabelle, Martinet Jérémie
UNIROUEN, Normandie université, Inserm U1234, FOCIS Center of Excellence, Pan'THER, Rouen F-76000, France.
Department of Pharmacy, Centre Henri Becquerel, Rouen F-76000, France.
Stem Cells Transl Med. 2025 Sep 11;14(9). doi: 10.1093/stcltm/szaf038.
Idiopathic inflammatory myopathies, commonly referred as myositis, are autoimmune diseases that cause muscle damage, progressive weakness, and disability. Current treatments, including corticosteroids and immunosuppressants, have significant limitations, highlighting the need for new therapies.
This preclinical study explored the therapeutic potential of adipose tissue-derived cell therapies, specifically stromal vascular fraction (SVF) and adipose-derived stem cells (ADSC), using an Icos-/- NOD mouse model of spontaneous myositis.
SVF and ADSC were extracted from CD1 female mice adipose tissue and cultured. Various doses were injected intramuscularly into the right hind limb of 20- to 22-week-old female Icos-/- NOD mice with a control group. The therapeutic effects were assessed through clinical scoring, grip strength test, and motor function analysis using Catwalk system. Muscle atrophy was evidenced by histology, and systemic inflammation was analyzed by flow cytometry.
Mice treated with either SVF or ADSC showed a dose-dependent slowdown in disease progression and improvements in motor functions, such as gait, movement, speed, and weight distribution between the legs. Histological analysis showed a reduction in muscular atrophy, particularly in the injected limb. Flow cytometry analysis on lymph nodes showed shifts in leukocyte populations, with reduced expression of inflammatory and activation markers.
Overall, this study demonstrated the therapeutic potential intramuscular injection of SVF or ADSC in the Icos-/- NOD mouse model of myositis, providing a proof-of-concept for the use of adipose tissue-derived cell therapies in the treatment of idiopathic inflammatory myopathies.
特发性炎性肌病,通常称为肌炎,是一种自身免疫性疾病,可导致肌肉损伤、进行性肌无力和残疾。目前的治疗方法,包括皮质类固醇和免疫抑制剂,有显著局限性,凸显了对新疗法的需求。
本临床前研究使用自发性肌炎的Icos-/- NOD小鼠模型,探索脂肪组织衍生细胞疗法,特别是基质血管成分(SVF)和脂肪来源干细胞(ADSC)的治疗潜力。
从CD1雌性小鼠脂肪组织中提取SVF和ADSC并进行培养。将不同剂量的细胞肌肉注射到20至22周龄的雌性Icos-/- NOD小鼠右后肢,设置一个对照组。通过临床评分、握力测试以及使用Catwalk系统进行运动功能分析来评估治疗效果。通过组织学证明肌肉萎缩,并通过流式细胞术分析全身炎症。
接受SVF或ADSC治疗的小鼠疾病进展呈剂量依赖性减缓,运动功能有所改善,如步态、运动、速度以及双腿之间的重量分布。组织学分析显示肌肉萎缩减少,尤其是在注射肢体。对淋巴结的流式细胞术分析显示白细胞群体发生变化,炎症和激活标志物的表达降低。
总体而言,本研究证明了在肌炎的Icos-/- NOD小鼠模型中肌肉注射SVF或ADSC的治疗潜力,为使用脂肪组织衍生细胞疗法治疗特发性炎性肌病提供了概念验证。