Borrelli Matthew A, Warunek Jordan Jp, Little Steven R, Turnquist Heth R
University of Pittsburgh.
University of Pittsburgh School of Medicine.
Res Sq. 2025 Aug 22:rs.3.rs-7237053. doi: 10.21203/rs.3.rs-7237053/v1.
Skeletal muscle injuries are a common consequence of physical activity, repetitive movements, and trauma. Regulatory T cells (Treg) have recently been identified as critical mediators of immune repair response after injury, and treatments effectively targeting Treg may accelerate injury resolution. CCL22 is a chemokine that recruits CCR4-expressing cells, particularly Treg, to sites of inflammation or immune regulation, such as tumor microenvironments. When a sustained release formulation of polymeric microparticles (MP) delivering CCL22 (CCL22MP), was administered after cardiotoxin (CTx)-mediated muscle injury, significantly improved limb function was observed on days 3 and 5 post injury. Histologic evaluation of the injured limbs showed reduced area of injury in CCL22MP treated limbs. Analysis of the local immune populations revealed augmented Treg concentrations, as well as increased myeloid derived suppressor cell and neutrophil frequency. These findings reveal that amplifying local Treg to damaged areas improves outcomes, thus offering a translationally promising approach after muscle injury.
骨骼肌损伤是体育活动、重复性动作和创伤的常见后果。调节性T细胞(Treg)最近被确定为损伤后免疫修复反应的关键介质,有效靶向Treg的治疗可能会加速损伤的愈合。CCL22是一种趋化因子,可将表达CCR4的细胞,特别是Treg募集到炎症或免疫调节部位,如肿瘤微环境。在心脏毒素(CTx)介导的肌肉损伤后给予递送CCL22的聚合物微粒(MP)缓释制剂(CCL22MP),在损伤后第3天和第5天观察到肢体功能显著改善。对受伤肢体的组织学评估显示,CCL22MP治疗的肢体损伤面积减小。对局部免疫细胞群的分析显示,Treg浓度增加,以及髓系来源的抑制细胞和中性粒细胞频率增加。这些发现表明,将局部Treg扩增到受损区域可改善预后,从而为肌肉损伤后提供了一种有转化前景的方法。