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脐带间充质干细胞治疗肌萎缩侧索硬化症:一项原创性研究。

Umbilical Cord Mesenchymal Stem Cells in Amyotrophic Lateral Sclerosis: an Original Study.

机构信息

Department of Neurosurgery, University of Warmia and Mazury, Olsztyn, Poland.

Instytut Terapii Komórkowych S.A., FamiCord Group, Olsztyn, Poland.

出版信息

Stem Cell Rev Rep. 2020 Oct;16(5):922-932. doi: 10.1007/s12015-020-10016-7.

Abstract

OBJECTIVE

Amyotrophic lateral sclerosis (ALS) is still incurable. Although different therapies can affect the health and survival of patients. Our aim is to evaluate the effect of umbilical mesenchymal stem cells administrated intrathecally to patients with amyotrophic lateral sclerosis on disability development and survival.

METHODS

This case-control study involved 67 patients treated with Wharton's jelly mesenchymal stem cells (WJ-MSC). The treated patients were paired with 67 reference patients from the PRO-ACT database which contains patient records from 23 ALS clinical studies (phase 2/3). Patients in the treatment and reference groups were fully matched in terms of race, sex, onset of symptoms (bulbar/spinal), FT9 disease stage at the beginning of therapy and concomitant amyotrophic lateral sclerosis medications. Progression rates prior to treatment varied within a range of ± 0.5 points. All patients received three intrathecal injections of Wharton's jelly-derived mesenchymal stem cells every two months at a dose of 30 × 10 cells. Patients were assessed using the ALSFRS-R scale. Survival times were followed-up until March 2020.

RESULTS

Median survival time increased two-fold in all groups. In terms of progression, three response types measured in ALSFRS-R were observed: decreased progression rate (n = 21, 31.3%), no change in progression rate (n = 33, 49.3%) and increased progression rate (n = 13, 19.4%). Risk-benefit ratios were favorable in all groups. No serious adverse drug reactions were observed.

INTERPRETATION

Wharton's jelly-derived mesenchymal stem cells therapy is safe and effective in some ALS patients, regardless of the clinical features and demographic factors excluding sex. The female sex and a good therapeutic response to the first administration are significant predictors of efficacy following further administrations. Graphical Abstract Medical therapeutic experiment with retrospective case-control analyses.

摘要

目的

肌萎缩侧索硬化症(ALS)仍然无法治愈。尽管不同的治疗方法可以影响患者的健康和生存,但我们的目的是评估鞘内给予脐带间充质干细胞对肌萎缩侧索硬化症患者残疾发展和生存的影响。

方法

这项病例对照研究涉及 67 名接受 Wharton 胶状间充质干细胞(WJ-MSC)治疗的患者。治疗组患者与来自 PRO-ACT 数据库的 67 名参考患者相匹配,该数据库包含 23 项 ALS 临床研究(2/3 期)的患者记录。治疗组和对照组患者在种族、性别、症状发作(球部/脊髓)、治疗开始时的 FT9 疾病阶段和伴随的肌萎缩侧索硬化症药物方面完全匹配。治疗前的进展率在±0.5 分范围内变化。所有患者每两个月接受三次鞘内注射剂量为 30×10 的 Wharton 胶状间充质干细胞细胞。使用 ALSFRS-R 量表对患者进行评估。生存时间随访至 2020 年 3 月。

结果

所有组的中位生存时间均延长了两倍。在进展方面,在 ALSFRS-R 中观察到三种反应类型:进展率降低(n=21,31.3%)、进展率不变(n=33,49.3%)和进展率增加(n=13,19.4%)。所有组的风险效益比均有利。未观察到严重的药物不良反应。

结论

无论临床特征和人口统计学因素(性别除外)如何,Wharton 胶状间充质干细胞治疗对某些肌萎缩侧索硬化症患者是安全有效的。女性性别和对首次给药的良好治疗反应是进一步给药后疗效的显著预测指标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f763/7456414/6da135f2c99d/12015_2020_10016_Figa_HTML.jpg

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