Alkhazaali-Ali Zahraa, Sahab-Negah Sajad, Boroumand Amir Reza, Farkhad Najmeh Kaffash, Khodadoust Mohammad Ali, Tavakol-Afshari Jalil
Department of Immunology, Immunology Research Center, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad 9177948959, Iran.
Student Research Committee, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad 9177948959, Iran.
Diseases. 2024 May 12;12(5):99. doi: 10.3390/diseases12050099.
Amyotrophic lateral sclerosis (ALS) is an incurable disease. There are vigorous attempts to develop treatments to reduce the effects of this disease, and among these treatments is the transplantation of stem cells. This study aimed to retrospectively evaluate a mesenchymal stem cell (MSC) therapy cohort as a promising novel treatment modality by estimating some additional new parameters, such as immunological and biochemical factors.
This study was designed as an open-label, one-arm cohort retrospective study to evaluate potential diagnostic biomarkers of repeated infusions of autologous-bone marrow-derived mesenchymal stem cells (BM-MSCs) in 15 confirmed patients with ALS, administered at a dose of 1 × 106 cells/kg BW with a one-month interval, in equal amounts in both an intravenous (IV) and intrathecal (IT) capacity simultaneously, via various biochemical (iron (Fe), ferritin, total-iron-binding capacity (TIBC), transferrin, and creatine kinase (CK)) and immunological parameters (tumor necrosis factor-alpha (TNF-α), neurofilament light chain (NFL), and glial-cell-derived neurotrophic factor (GDNF) levels, evaluated during the three-month follow-up period in serum and cerebrospinal fluid (CSF).
Our study indicated that, in the case of immunological biomarkers, TNF-α levels in the CSF showed a significant decrease at month three after transplantation compared with levels at month zero, and the -value was < 0.01. No statistically significant changes were observed for other immunological as well as biochemical parameters and a -value of > 0.05.
These results can indicate the potential benefit of stem cell transfusion in patients with ALS and suggest some diagnostic biomarkers. Several studies are required to approve these results.
肌萎缩侧索硬化症(ALS)是一种无法治愈的疾病。人们正在积极尝试开发治疗方法以减轻这种疾病的影响,其中包括干细胞移植。本研究旨在通过评估一些额外的新参数,如免疫和生化因素,回顾性地评估间充质干细胞(MSC)治疗队列作为一种有前景的新型治疗方式。
本研究设计为一项开放标签、单臂队列回顾性研究,以评估15例确诊的ALS患者重复输注自体骨髓来源的间充质干细胞(BM-MSC)的潜在诊断生物标志物,剂量为1×10⁶ 细胞/kg体重,间隔1个月,通过静脉(IV)和鞘内(IT)同时等量给药,在3个月的随访期内通过各种生化参数(铁(Fe)、铁蛋白、总铁结合能力(TIBC)、转铁蛋白和肌酸激酶(CK))和免疫参数(肿瘤坏死因子-α(TNF-α)、神经丝轻链(NFL)和胶质细胞源性神经营养因子(GDNF)水平)在血清和脑脊液(CSF)中进行评估。
我们的研究表明,就免疫生物标志物而言,与第0个月的水平相比,移植后第3个月脑脊液中TNF-α水平显著降低,P值<0.01。其他免疫和生化参数未观察到统计学上的显著变化,P值>0.05。
这些结果可以表明干细胞输注对ALS患者的潜在益处,并提示一些诊断生物标志物。需要多项研究来证实这些结果。