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间充质基质细胞(MSC)治疗重度类固醇难治性急性移植物抗宿主病(GVHD)

Treatment of severe steroid resistant acute GVHD with mesenchymal stromal cells (MSC).

作者信息

Resnick Igor B, Barkats Claudine, Shapira Michael Y, Stepensky Polina, Bloom Allan I, Shimoni Avichai, Mankuta David, Varda-Bloom Nira, Rheingold Lyudmila, Yeshurun Moshe, Bielorai Bella, Toren Amos, Zuckerman Tsila, Nagler Arnon, Or Reuven

机构信息

Department of Bone Marrow Transplantation and Cancer Immunotherapy, Hadassah-Hebrew University Medical Center Jerusalem.

出版信息

Am J Blood Res. 2013 Aug 19;3(3):225-38. eCollection 2013.

Abstract

BACKGROUND

Several studies revealed that MSC from human bone marrow can downregulate graft-versus-host disease (GVHD) after allogeneic HSCT.

METHODS

Herein we present 50 patients with acute GVHD who got 74 (1-4) MSC infusions for 54 separate episodes of aGVHD.

RESULTS

aGVHD was defined as steroid resistant grade IV aGVHD in 42 cases. The major presentation was gastrointestinal GVHD; two (n=18) or more (n=21) systems were involved in the majority of cases. The 1(st) infusion with MSC was given on day +27 (range, 1 to 136); d+45 (range, +11 to +150) post diagnosis of aGVHD and HSCT, respectively. In 2/3 of the cases treatment was performed with frozen stocked MSCs; in 62 cases early passages (1-3) were used. The median number of infused cells was 1.14±0.47 million per kg in the first injection and up to 4.27 (1.70±1.10) millions in total. The two patients with aggressive liver GVHD received MSCs injections intra hepatic arteries without changes of blood flow or evidence cytolysis, but also without a visible effect. Disease free survival at 3.6 years was 56%. We observed better overall survival in patients with GVHD grade < 4, in responders to the 1(st) treatment with MSC, and in pediatric group. The multivariate analysis demonstrated independent influence on survival of initial response and younger age. There were no immediate or late toxicity or side effects.

CONCLUSION

Injection of MSCs seems to be a promising and safe treatment of GVHD. The encouraging results obviously should be confirmed in a randomized prospective study.

摘要

背景

多项研究表明,人骨髓间充质干细胞(MSC)可下调异基因造血干细胞移植(HSCT)后的移植物抗宿主病(GVHD)。

方法

本文报告了50例急性GVHD患者,他们接受了74次(1 - 4次)MSC输注,用于治疗54次单独发作的急性移植物抗宿主病(aGVHD)。

结果

42例患者的aGVHD被定义为对类固醇耐药的IV级aGVHD。主要表现为胃肠道GVHD;大多数病例涉及两个(n = 18)或更多(n = 21)系统。首次输注MSC在+27天(范围1至136天);分别在aGVHD和HSCT诊断后的+45天(范围+11至+150天)。2/3的病例使用冷冻保存的MSC进行治疗;62例使用早期传代(1 - 3代)的细胞。首次注射时每公斤输注细胞的中位数为114±47万,总共高达427万(170±110万)。两名患有侵袭性肝脏GVHD的患者接受了肝动脉内MSC注射,血流无变化,也无细胞溶解证据,但也没有明显效果。3.6年时的无病生存率为56%。我们观察到GVHD分级<4级的患者、对首次MSC治疗有反应的患者以及儿童组的总生存率更高。多变量分析表明初始反应和年轻对生存率有独立影响。没有立即或晚期毒性或副作用。

结论

注射MSC似乎是一种有前景且安全的GVHD治疗方法。这些令人鼓舞的结果显然应在随机前瞻性研究中得到证实。

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