Cataldi Marcela P, Vannoy Charles H, Blaeser Anthony, Tucker Jason D, Leroy Victoria, Rawls Raegan, Killilee Jessalyn, Holbrook Molly C, Lu Qi Long
McColl-Lockwood Laboratory for Muscular Dystrophy Research, Cannon Research Center, Carolinas Medical Center, Atrium Health, Charlotte, NC 28203, USA.
McColl-Lockwood Laboratory for Muscular Dystrophy Research, Cannon Research Center, Carolinas Medical Center, Atrium Health, Charlotte, NC 28203, USA.
Mol Ther. 2023 Dec 6;31(12):3478-3489. doi: 10.1016/j.ymthe.2023.10.022. Epub 2023 Nov 2.
Mutations in the fukutin-related protein (FKRP) gene cause dystroglycanopathy, with disease severity ranging from mild LGMD2I to severe congenital muscular dystrophy. Recently, considerable progress has been made in developing experimental therapies, with adeno-associated virus (AAV) gene therapy and ribitol treatment demonstrating significant therapeutic effect. However, each treatment has its strengths and weaknesses. AAV gene therapy can achieve normal levels of transgene expression, but it requires high doses, with toxicity concerns and variable distribution. Ribitol relies on residual FKRP function and restores limited levels of matriglycan. We hypothesized that these two treatments can work synergistically to offer an optimized therapy with efficacy and safety unmatched by each treatment alone. The most effective treatment is the combination of high-dose (5e-13 vg/kg) AAV-FKRP with ribitol, whereas low dose (1e-13 vg/kg) AAV-FKRP combined with ribitol showed a 22.6% increase in positive matriglycan fibers and the greater improvement in pathology when compared to low-dose AAV-FKRP alone. Together, our results support the potential benefits of combining ribitol with AAV gene therapy for treating FKRP-related muscular dystrophy. The fact that ribitol is a metabolite in nature and has already been tested in animal models and clinical trials in humans without severe side effects provides a safety profile for it to be trialed in combination with AAV gene therapy.
福金蛋白相关蛋白(FKRP)基因突变会导致糖基化肌营养不良症,疾病严重程度从轻度的肢带型肌营养不良2I型到严重的先天性肌营养不良不等。最近,在开发实验性疗法方面取得了重大进展,腺相关病毒(AAV)基因疗法和核糖醇治疗均显示出显著的治疗效果。然而,每种治疗方法都有其优缺点。AAV基因疗法可以实现转基因表达的正常水平,但需要高剂量,存在毒性问题且分布不均。核糖醇依赖于残余的FKRP功能,只能恢复有限水平的基质糖。我们假设这两种治疗方法可以协同作用,提供一种优化的疗法,其疗效和安全性是单独使用每种治疗方法所无法比拟的。最有效的治疗方法是高剂量(5×10^-13病毒基因组/千克)的AAV-FKRP与核糖醇联合使用,而低剂量(1×10^-13病毒基因组/千克)的AAV-FKRP与核糖醇联合使用时,与单独使用低剂量AAV-FKRP相比,阳性基质糖纤维增加了22.6%,病理学改善更明显。总之,我们的结果支持了核糖醇与AAV基因疗法联合治疗FKRP相关肌营养不良症的潜在益处。核糖醇是一种天然代谢产物,已经在动物模型和人体临床试验中进行了测试,且无严重副作用,这为其与AAV基因疗法联合试验提供了安全性依据。