Erkers Tom, Kaipe Helen, Nava Silvia, Molldén Pia, Gustafsson Britt, Axelsson Rimma, Ringdén Olle
1 Division of Therapeutic Immunology, Department of Laboratory Medicine, Center for Allogeneic Stem Cell Transplantation, Karolinska Institutet and Karolinska University Hospital , Stockholm, Sweden .
Stem Cells Dev. 2015 Jan 15;24(2):253-63. doi: 10.1089/scd.2014.0265.
Decidual stromal cells (DSCs) isolated from fetal membranes of term placentas are easily expanded and are highly immunosuppressive in vitro. These cells express high levels of integrins that are of importance in homing to inflamed tissues. In this study, we investigated DSCs as a cellular therapy for chronic graft-versus-host disease (cGvHD), a severe complication after allogeneic hematopoietic stem cell transplantation. Subsequent to transplantation, three patients developed severe extensive cGvHD and were treated with DSCs (1-2.8 × 10(6) cells/kg). One-third of the DSCs administered to two patients were labeled with (111)Indium, and the in vivo distribution was tracked for 48 h. The (111)In-labeled DSCs were initially located in the lungs, followed by dissemination to the liver and spleen. The DSCs induced a partial response in two of the patients. Blood samples from the patients were extensively evaluated by flow cytometry, luminex, and enzyme-linked immunosorbent assay. The nonresponder had the highest proportion of T-cells with Th17 and Th2 phenotypes and the highest median plasma concentrations of IL-17 and IL-4. The same patient also had high frequencies of HLA-DR(+) T-cells and regulatory T-cells. To conclude, DSCs are safe to infuse with no adverse effects. We determined how stromal cells are distributed in vivo after infusion in a cGvHD setting. The methods established for analysis of blood samples will be useful in determining the effect of DSCs in a study comprising a larger patient material. This pilot study may provide a basis for further controlled investigations with DSCs in a clinical setting.
从足月胎盘胎膜中分离出的蜕膜基质细胞(DSCs)易于扩增,且在体外具有高度免疫抑制作用。这些细胞表达高水平的整合素,这对归巢至炎症组织很重要。在本研究中,我们研究了将DSCs作为慢性移植物抗宿主病(cGvHD)的细胞治疗方法,cGvHD是同种异体造血干细胞移植后的一种严重并发症。移植后,三名患者发生了严重的广泛性cGvHD,并接受了DSCs治疗(1 - 2.8×10⁶个细胞/千克)。给两名患者输注的DSCs中有三分之一用¹¹¹铟标记,并追踪其体内分布48小时。¹¹¹铟标记的DSCs最初位于肺部,随后扩散至肝脏和脾脏。DSCs在两名患者中诱导了部分反应。通过流式细胞术、Luminex和酶联免疫吸附测定对患者的血样进行了广泛评估。无反应者具有最高比例的Th17和Th2表型T细胞以及最高的IL - 17和IL - 4血浆中位浓度。同一名患者还具有高频率的HLA - DR⁺ T细胞和调节性T细胞。总之,输注DSCs是安全的,没有不良反应。我们确定了在cGvHD环境中输注后基质细胞在体内的分布情况。所建立的血样分析方法将有助于在包含更大患者样本的研究中确定DSCs的效果。这项初步研究可能为在临床环境中对DSCs进行进一步对照研究提供基础。