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CellKine临床试验:关于同种异体骨髓间充质干细胞用于疼痛性腰椎小关节病受试者的1期试验的首次报告。

CellKine clinical trial: first report from a phase 1 trial of allogeneic bone marrow-derived mesenchymal stem cells in subjects with painful lumbar facet joint arthropathy.

作者信息

Yan Dan, Zubair Abba C, Osborne Michael D, Pagan-Rosado Robert, Stone Jeffrey A, Lehman Vance T, Durand Nisha C, Kubrova Eva, Wang Zhen, Witter Drew M, Baer Meghan M, Ponce Gabriela C, Quiñones-Hinojosa Alfredo, Qu Wenchun

机构信息

Department of Pain Medicine, Mayo Clinic, Jacksonville, FL, USA.

Transfusion Medicine, Department of Pathology, Mayo Clinic, Jacksonville, FL, USA.

出版信息

Pain Rep. 2024 Sep 18;9(5):e1181. doi: 10.1097/PR9.0000000000001181. eCollection 2024 Oct.

Abstract

BACKGROUND

Lumbar facet joint arthropathy (LFJA) is a major cause of low back pain (LBP), with current treatments offering limited long-term benefits. Bone marrow-derived mesenchymal stem cells (BM-MSCs) show promise due to their immunomodulatory and trophic effects, potentially addressing underlying degenerative processes in LFJA.

OBJECTIVES

This initial report describes the outcomes of the first treated patient in an ongoing mutidisciplinary phase 1 clinical trial evaluating the safety and feasibility of intra-articular allogeneic BM-MSCs for painful LFJA.

METHODS

Following enrollment in our IRB-approved protocol, symptomatic LFJA was confirmed through double blocks on L4 and L5 medial branches. Two 1-mL syringes, each containing 10 million BM-MSCs, were prepared in the cGMP facility and administered bilaterally to the patient's L4-L5 lumbar facet joints. The patient underwent standardized follow-ups, including clinical examinations and functional and imaging assessments for 2 years, utilizing patient-reported outcomes measurement information system-computer adaptive tests (PROMIS CATs), visual analogue scale, Oswestry disability index, work functional status and opioid pain medication use, and MR imaging Fenton-Czervionke score.

RESULTS

The patient tolerated the procedure well, with no drug-related adverse events during the study period. Pain, spine function, and work functional status improved at multiple follow-ups. This patient also reported improvements in mental and social health, along with a notable improvement in the grade of facet synovitis observed at the one-year follow-up MRI evaluation.

CONCLUSIONS

This case report suggests the safety and feasibility of administering intra-articular allogeneic BM-MSCs, offering therapeutic benefits for pain management and functional activities.

摘要

背景

腰椎小关节病(LFJA)是下腰痛(LBP)的主要原因,目前的治疗方法长期疗效有限。骨髓间充质干细胞(BM-MSCs)因其免疫调节和营养作用显示出前景,可能解决LFJA潜在的退行性病变过程。

目的

本初步报告描述了一项正在进行的多学科1期临床试验中首例接受治疗患者的结果,该试验评估关节内同种异体BM-MSCs治疗疼痛性LFJA的安全性和可行性。

方法

在我们经机构审查委员会批准的方案入组后,通过对L4和L5内侧支进行双重阻滞确认有症状的LFJA。在符合cGMP标准的设施中制备两个1毫升注射器,每个注射器含有1000万个BM-MSCs,并双侧注射到患者的L4-L5腰椎小关节。患者接受了标准化随访,包括为期2年的临床检查、功能和影像学评估,采用患者报告结局测量信息系统-计算机自适应测试(PROMIS CATs)、视觉模拟量表、Oswestry功能障碍指数、工作功能状态和阿片类止痛药物使用情况,以及磁共振成像Fenton-Czervionke评分。

结果

患者对该操作耐受性良好,研究期间未出现与药物相关的不良事件。在多次随访中,疼痛、脊柱功能和工作功能状态均有所改善。该患者还报告了心理和社会健康状况的改善,以及在1年随访磁共振成像评估中观察到的小关节滑膜炎等级有显著改善。

结论

本病例报告表明关节内注射同种异体BM-MSCs具有安全性和可行性,对疼痛管理和功能活动具有治疗益处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5be/11412710/c62563328463/painreports-9-e1181-g001.jpg

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