一项评估脐带间充质干细胞治疗膝骨关节炎的安全性和有效性的 I 期剂量递增临床试验。

A Phase I Dose-Escalation Clinical Trial to Assess the Safety and Efficacy of Umbilical Cord-Derived Mesenchymal Stromal Cells in Knee Osteoarthritis.

机构信息

Centro de Terapia Celular, Clínica Universidad de los Andes, Santiago, Chile.

IMPACT, Center of Interventional Medicine for Precision and Advanced Cellular Therapy, Santiago, Chile.

出版信息

Stem Cells Transl Med. 2024 Mar 15;13(3):193-203. doi: 10.1093/stcltm/szad088.

Abstract

Osteoarthritis (OA) is the most common degenerative joint disease. Mesenchymal stromal cells (MSC) are promising cell-based therapy for OA. However, there is still a need for additional randomized, dose-dependent studies to determine the optimal dose and tissue source of MSC for improved clinical outcomes. Here, we performed a dose-dependant evaluation of umbilical cord (UC)-derived MSC (Celllistem) in a murine model and in knee OA patients. For the preclinical study, a classical dose (200.000 cells) and a lower dose (50.000 cells) of Cellistem were intra-articularly injected into the mice knee joints. The results showed a dose efficacy response effect of Cellistem associated with a decreased inflammatory and degenerative response according to the Pritzker OARSI score. Following the same approach, the dose-escalation phase I clinical trial design included 3 sequential cohorts: low-dose group (2 × 106 cells), medium-dose group (20 × 106), and high-dose group (80 × 106). All the doses were safe, and no serious adverse events were reported. Nonetheless, 100% of the patients injected with the high-dose experienced injection-related swelling in the knee joint. According to WOMAC total outcomes, patients treated with all doses reported significant improvements in pain and function compared with baseline after 3 and 6 months. However, the improvements were higher in patients treated with both medium and low dose as compared to high dose. Therefore, our data demonstrate that the intra-articular injection of different doses of Cellistem is both safe and efficient, making it an interesting therapeutic alternative to treat mild and symptomatic knee OA patients. Trial registration ClinicalTrials.gov NCT03810521.

摘要

骨关节炎(OA)是最常见的退行性关节疾病。间充质基质细胞(MSC)是一种有前途的 OA 细胞治疗方法。然而,仍需要更多的随机、剂量依赖性研究来确定 MSC 的最佳剂量和组织来源,以获得更好的临床结果。在这里,我们在小鼠模型和膝骨关节炎患者中进行了脐带(UC)衍生 MSC(Celllistem)的剂量依赖性评估。在临床前研究中,将 Cellistem 的经典剂量(200,000 个细胞)和较低剂量(50,000 个细胞)关节内注射到小鼠膝关节中。结果显示,Cellistem 存在剂量疗效反应,根据 Pritzker OARSI 评分,炎症和退行性反应降低。采用相同方法,剂量递增 I 期临床试验设计包括 3 个连续队列:低剂量组(2×106 个细胞)、中剂量组(20×106)和高剂量组(80×106)。所有剂量均安全,未报告严重不良事件。尽管如此,高剂量组注射的所有患者均出现膝关节注射相关肿胀。根据 WOMAC 总结局,与基线相比,所有剂量治疗的患者在 3 个月和 6 个月后报告疼痛和功能显著改善。然而,与高剂量相比,中剂量和低剂量治疗的患者改善更高。因此,我们的数据表明,关节内注射不同剂量的 Cellistem 既安全又有效,是治疗轻度和有症状的膝骨关节炎患者的一种有前途的治疗选择。临床试验注册ClinicalTrials.gov NCT03810521。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a21e/10940813/255c913db2a7/szad088_fig5.jpg

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