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干细胞移植治疗多发性硬化症的疗效和安全性:系统评价和随机对照试验的荟萃分析。

Efficacy and safety of stem cell transplantation for multiple sclerosis: a systematic review and meta-analysis of randomized controlled trials.

机构信息

Faculty of Medicine, Zagazig University, Zagazig, Egypt.

Faculty of Dentistry, Suez Canal University, Ismailia, Egypt.

出版信息

Sci Rep. 2024 May 31;14(1):12545. doi: 10.1038/s41598-024-62726-4.

Abstract

Multiple sclerosis (MS) is a common autoimmune neurological disease affecting patients' motor, sensory, and visual performance. Stem Cell Transplantation (SCT) is a medical intervention where a patient is infused with healthy stem cells with the purpose of resetting their immune system. SCT shows remyelinating and immunomodulatory functions in MS patients, representing a potential therapeutic option. We conducted this systematic review and meta-analysis that included randomized control trials (RCTs) of SCT in MS patients to investigate its clinical efficacy and safety, excluding observational and non-English studies. After systematically searching PubMed, Web of Science, Scopus, and Cochrane Library until January 7, 2024, nine RCTs, including 422 patients, were eligible. We assessed the risk of bias (ROB) in these RCTs using Cochrane ROB Tool 1. Data were synthesized using Review Manager version 5.4 and OpenMeta Analyst software. We also conducted subgroup and sensitivity analyses. SCT significantly improved patients expanded disability status scale after 2 months (N = 39, MD =  - 0.57, 95% CI [- 1.08, - 0.06], p = 0.03). SCT also reduced brain lesion volume (N = 136, MD = - 7.05, 95% CI [- 10.69, - 3.4], p = 0.0002). The effect on EDSS at 6 and 12 months, timed 25-foot walk (T25-FW), and brain lesions number was nonsignificant. Significant adverse events (AEs) included local reactions at MSCs infusion site (N = 25, RR = 2.55, 95% CI [1.08, 6.03], p = 0.034) and hematological disorders in patients received immunosuppression and autologous hematopoietic SCT (AHSCT) (N = 16, RR = 2.33, 95% CI [1.23, 4.39], p = 0.009). SCT can improve the disability of MS patients and reduce their brain lesion volume. The transplantation was generally safe and tolerated, with no mortality or significant serious AEs, except for infusion site reactions after mesenchymal SCT and hematological AEs after AHSCT. However, generalizing our results is limited by the sparse number of RCTs conducted on AHSCT. Our protocol was registered on PROSPERO with a registration number: CRD42022324141.

摘要

多发性硬化症(MS)是一种常见的自身免疫性神经系统疾病,影响患者的运动、感觉和视觉功能。干细胞移植(SCT)是一种医疗干预措施,通过输注健康的干细胞来重置患者的免疫系统。SCT 在 MS 患者中具有髓鞘再生和免疫调节功能,是一种有潜力的治疗选择。我们进行了这项系统评价和荟萃分析,纳入了 SCT 治疗 MS 患者的随机对照试验(RCT),以研究其临床疗效和安全性,排除了观察性和非英语研究。我们系统地检索了 PubMed、Web of Science、Scopus 和 Cochrane Library,直到 2024 年 1 月 7 日,共纳入了 9 项 RCT,包括 422 名患者。我们使用 Cochrane ROB Tool 1 评估了这些 RCT 的偏倚风险(ROB)。使用 Review Manager 版本 5.4 和 OpenMeta Analyst 软件综合数据。我们还进行了亚组和敏感性分析。SCT 可显著改善患者治疗 2 个月后的扩展残疾状况量表(N=39,MD=-0.57,95%CI[-1.08,-0.06],p=0.03)。SCT 还可减少脑病变体积(N=136,MD=-7.05,95%CI[-10.69,-3.4],p=0.0002)。但对 6 个月和 12 个月时的 EDSS、25 英尺步行(T25-FW)和脑病变数量的影响不显著。有意义的不良事件(AE)包括间充质干细胞输注部位的局部反应(N=25,RR=2.55,95%CI[1.08,6.03],p=0.034)和接受免疫抑制和自体造血干细胞移植(AHSCT)的患者的血液学障碍(N=16,RR=2.33,95%CI[1.23,4.39],p=0.009)。SCT 可改善 MS 患者的残疾状况并减少其脑病变体积。该移植一般安全耐受,无死亡或严重不良事件,但除间充质 SCT 后输注部位反应和 AHSCT 后血液学 AE 外。然而,由于 AHSCT 的 RCT 数量较少,我们的结果存在一定的局限性。我们的方案已在 PROSPERO 上注册,注册号为:CRD42022324141。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6de5/11143245/567dfbc6c391/41598_2024_62726_Fig1_HTML.jpg

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