BioXcellerator/ BioXscience Advanced Therapies and Translational Medicine, Medellín, Antioquia, Colombia.
Universidad Nacional de Colombia, Medellín, Antioquia, Colombia.
Stem Cell Res Ther. 2024 May 20;15(1):146. doi: 10.1186/s13287-024-03748-7.
Based on previous in vivo studies and human trials, intrathecal cell delivery is a safe and relevant therapeutic tool for improving patient's quality of life with neurological conditions. We aimed to characterise the safety profile of intrathecally delivered Mesenchymal stem cells (MSCs).
Ovid MEDLINE, Embase, Scopus, Cochrane Library, KCI-Korean Journal Database, and Web of Science. Databases were searched from their inception until April 13, 2023. Randomised Controlled Trials (RCTs) that compared intrathecal delivery of MSCs to controls in adult populations were included. Adverse events (AEs) were pooled and meta-analysed using DerSimonian-Laird random effects models with a correction factor 0.5 added to studies with zero count cells. Pooled AEs were described using Risk ratio (RR) and 95% confidence intervals (95% CI). Then, a random-effects meta-regress model on study-level summary data was performed to explore the relationship between the occurrence of AEs and covariates thought to modify the overall effect estimate. Finally, publication bias was assessed.
303 records were reviewed, and nine RCTs met the inclusion criteria and were included in the quantitative synthesis (n = 540 patients). MSCs delivered intrathecally, as compared to controls, were associated with an increased probability of AEs of musculoskeletal and connective tissue disorders (categorised by Common Terminology Criteria for Adverse Events-CTCAE version 5.0) (RR: 1.61, 95% CI 1.19-2.19, I = 0%). The random-effects meta-regress model suggested that fresh MSCs increased the probability of occurrence of AEs compared to cryopreserved MSCs (RR: 1.554; p-value = 0.048; 95% CI 1.004-2.404), and the multiple-dose, decreased the probability of AEs by 36% compared to single doses (RR: 0.644; p-value = 0.048; 95% CI 0.416-0.996); however, univariate random effects meta-regression models revealed a not significant association between the occurrence of AEs from MSCs intrathecal delivery and each covariate.
Intrathecal delivery of MSCs was associated with a slight increase in AEs associated with musculoskeletal and connective tissue disorders, albeit without serious AEs. We conclude that intrathecal MSCs delivery is safe for patients with neurological conditions. However, further high-quality, large-scale RCTs are needed to confirm these findings.
基于先前的体内研究和人体试验,鞘内细胞输送是一种安全且相关的治疗工具,可提高患有神经疾病患者的生活质量。我们旨在描述鞘内给予间充质干细胞(MSCs)的安全性特征。
检索 Ovid MEDLINE、Embase、Scopus、Cochrane 图书馆、KCI-Korean Journal Database 和 Web of Science。从数据库成立到 2023 年 4 月 13 日进行检索。纳入比较鞘内给予 MSCs 与成人人群中对照组的随机对照试验(RCT)。使用具有添加校正因子 0.5 的 DerSimonian-Laird 随机效应模型对不良事件(AE)进行汇总和荟萃分析,该校正因子适用于细胞计数为零的研究。使用风险比(RR)和 95%置信区间(95%CI)描述汇总的 AE。然后,对研究水平汇总数据进行随机效应荟萃回归模型分析,以探讨 AE 的发生与被认为可改变总体效应估计的协变量之间的关系。最后,评估发表偏倚。
共审查了 303 条记录,符合纳入标准的 9 项 RCT 被纳入定量综合分析(n=540 例患者)。与对照组相比,鞘内给予 MSCs 与肌肉骨骼和结缔组织疾病的 AE 发生率增加有关(根据不良事件通用术语标准-CTCAE 版本 5.0 进行分类)(RR:1.61,95%CI 1.19-2.19,I=0%)。随机效应荟萃回归模型表明,与冷冻保存的 MSCs 相比,新鲜 MSCs 增加了 AE 发生的可能性(RR:1.554;p 值=0.048;95%CI 1.004-2.404),而多次剂量与单次剂量相比,AE 发生率降低了 36%(RR:0.644;p 值=0.048;95%CI 0.416-0.996);然而,单变量随机效应荟萃回归模型显示,鞘内给予 MSCs 引起的 AE 与每个协变量之间的关联没有统计学意义。
鞘内给予 MSCs 与肌肉骨骼和结缔组织疾病相关的 AE 略有增加,但没有严重的 AE。我们得出结论,鞘内 MSCs 输送对患有神经疾病的患者是安全的。然而,需要进一步开展高质量、大规模的 RCT 来证实这些发现。