Department of Gastroenterology and Hepatology, Leiden University Medical Center, Albinusdreef 2, 2333 ZA Leiden, The Netherlands.
Gut. 2010 Dec;59(12):1662-9. doi: 10.1136/gut.2010.215152. Epub 2010 Oct 4.
Mesenchymal stromal cells (MSCs) are pluripotent cells that have immunosuppressive effects both in vitro and in experimental colitis. Promising results of MSC therapy have been obtained in patients with severe graft versus host disease of the gut. Our objective was to determine the safety and feasibility of autologous bone marrow derived MSC therapy in patients with refractory Crohn's disease.
10 adult patients with refractory Crohn's disease (eight females and two males) underwent bone marrow aspiration under local anaesthesia. Bone marrow MSCs were isolated and expanded ex vivo. MSCs were tested for phenotype and functionality in vitro. 9 patients received two doses of 1-2×10(6) cells/kg body weight, intravenously, 7 days apart. During follow-up, possible side effects and changes in patients' Crohn's disease activity index (CDAI) scores were monitored. Colonoscopies were performed at weeks 0 and 6, and mucosal inflammation was assessed by using the Crohn's disease endoscopic index of severity.
MSCs isolated from patients with Crohn's disease showed similar morphology, phenotype and growth potential compared to MSCs from healthy donors. Importantly, immunomodulatory capacity was intact, as Crohn's disease MSCs significantly reduced peripheral blood mononuclear cell proliferation in vitro. MSC infusion was without side effects, besides a mild allergic reaction probably due to the cryopreservant DMSO in one patient. Baseline median CDAI was 326 (224-378). Three patients showed clinical response (CDAI decrease ≥70 from baseline) 6 weeks post-treatment; conversely three patients required surgery due to disease worsening.
Administration of autologous bone marrow derived MSCs appears safe and feasible in the treatment of refractory Crohn's disease. No serious adverse events were detected during bone marrow harvesting and administration.
间充质基质细胞(MSCs)是一种多能细胞,在体外和实验性结肠炎中均具有免疫抑制作用。MSC 治疗在严重肠道移植物抗宿主病的患者中取得了有希望的结果。我们的目的是确定自体骨髓来源 MSC 治疗难治性克罗恩病患者的安全性和可行性。
10 名成年难治性克罗恩病患者(8 名女性和 2 名男性)在局部麻醉下接受骨髓抽吸。从骨髓中分离和体外扩增 MSC。在体外测试 MSC 的表型和功能。9 名患者接受了两次剂量为 1-2×10(6)个细胞/kg 体重的静脉内输注,间隔 7 天。在随访期间,监测患者的可能副作用和克罗恩病活动指数(CDAI)评分的变化。在 0 周和 6 周时进行结肠镜检查,并使用克罗恩病内镜严重程度指数评估黏膜炎症。
从克罗恩病患者中分离的 MSC 与来自健康供体的 MSC 具有相似的形态、表型和生长潜力。重要的是,免疫调节能力是完整的,因为克罗恩病 MSC 显著降低了体外外周血单核细胞的增殖。MSC 输注无副作用,除了一名患者可能由于冷冻保存剂 DMSO 而出现轻度过敏反应。基线中位数 CDAI 为 326(224-378)。3 名患者在治疗后 6 周出现临床反应(CDAI 从基线下降≥70);相反,3 名患者因病情恶化而需要手术。
自体骨髓来源 MSC 的给药在治疗难治性克罗恩病中似乎是安全可行的。在骨髓采集和给药过程中未发现严重不良事件。