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异体造血干细胞移植后接受第三方间充质基质细胞治疗的患者细胞免疫组分的改变。

Alterations in the cellular immune compartment of patients treated with third-party mesenchymal stromal cells following allogeneic hematopoietic stem cell transplantation.

机构信息

Department of Medicine, Karolinska Institutet, Hematology Center, Karolinska University Hospital, Stockholm, Sweden.

出版信息

Stem Cells. 2013 Aug;31(8):1715-25. doi: 10.1002/stem.1386.

Abstract

Adoptive transfer of third-party mesenchymal stromal cells (MSCs) has emerged as a promising tool for the treatment of steroid-refractory graft-versus-host disease (GVHD). Despite numerous in vitro studies and preclinical models, little is known about their effects on the patients' immune system. We assessed immune alterations in the T-cell, B-cell, natural killer cell, dendritic cell, and monocytic compartments of steroid-refractory GVHD patients 30, 90, and 180 days after MSC (n = 6) or placebo (n = 5) infusion, respectively. Infused MSCs were bioactive as suggested by the significant reduction in epithelial cell death, which represents a biomarker for acute GVHD. There were several indications that MSCs shift the patients' immune system toward a more tolerogenic profile. Most importantly, infusion of MSCs was associated with increased levels of regulatory (forkhead box P3 (FOXP3)(+) and interleukin (IL)-10(+) ) T-cells, reduced pro-inflammatory IL-17(+) T(Th17)-cells, and skewing toward type-2 T-helper cell responses. Furthermore, IL-2, which has been recently shown to exert a positive immune modulating effect in GVHD patients, was higher in the MSC patients at all evaluated time points during 6 months after MSC-infusion. Overall, our findings will contribute to the refinement of monitoring tools, for assessing MSC treatment-efficacy and increase our understanding regarding the MSCs' in vivo effects.

摘要

采用第三方间充质基质细胞(MSCs)已成为治疗类固醇难治性移植物抗宿主病(GVHD)的有前途的工具。尽管有许多体外研究和临床前模型,但对它们对患者免疫系统的影响知之甚少。我们评估了类固醇难治性 GVHD 患者在 MSC(n = 6)或安慰剂(n = 5)输注后 30、90 和 180 天的 T 细胞、B 细胞、自然杀伤细胞、树突状细胞和单核细胞中的免疫改变。输注的 MSC 具有生物活性,因为上皮细胞死亡的显著减少表明急性 GVHD 的生物标志物。有几个迹象表明 MSC 将患者的免疫系统转向更耐受的表型。最重要的是,MSC 的输注与调节性(叉头框 P3(FOXP3)(+)和白细胞介素(IL)-10(+))T 细胞水平升高、促炎性 IL-17(+)T(Th17)-细胞减少以及向 2 型辅助性 T 细胞反应倾斜有关。此外,最近在 GVHD 患者中显示出积极的免疫调节作用的 IL-2 在 MSC 患者中在 MSC 输注后 6 个月的所有评估时间点均较高。总体而言,我们的发现将有助于改进监测工具,以评估 MSC 治疗效果,并增加我们对 MSC 体内作用的理解。

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