Treatment of Severe Chronic Graft-Versus-Host Disease with Decidual Stromal Cells and Tracing with 111Indium Radiolabeling

被引:43
作者
Erkers, Tom [1 ,2 ]
Kaipe, Helen [1 ,2 ]
Nava, Silvia [1 ,2 ]
Mollden, Pia [1 ,2 ]
Gustafsson, Britt [2 ,3 ]
Axelsson, Rimma [2 ,3 ]
Ringden, Olle [1 ,2 ]
机构
[1] Karolinska Inst, Div Therapeut Immunol, Dept Lab Med, Ctr Allogene Stem Cell Transplantat, S-14186 Stockholm, Sweden
[2] Karolinska Univ Hosp, S-14186 Stockholm, Sweden
[3] Karolinska Inst, Dept Clin Sci Intervent & Technol, S-14186 Stockholm, Sweden
基金
瑞典研究理事会;
关键词
MESENCHYMAL STEM-CELLS; BONE-MARROW; PERIPHERAL-BLOOD; FETAL MEMBRANE; T-CELLS; TRANSPLANTATION; RESISTANT; ASSOCIATION; CONTACT; THERAPY;
D O I
10.1089/scd.2014.0265
中图分类号
Q813 [细胞工程];
学科分类号
摘要
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 (1-2.8x10(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 In-111-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.
引用
收藏
页码:253 / 263
页数:11
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