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首页> 外文期刊>Stem Cells >Bone marrow mesenchymal stromal cells to treat tissue damage in allogeneic stem cell transplant recipients: Correlation of biological markers with clinical responses
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Bone marrow mesenchymal stromal cells to treat tissue damage in allogeneic stem cell transplant recipients: Correlation of biological markers with clinical responses

机译:骨髓间充质基质细胞治疗同种异体干细胞移植受者的组织损伤:生物学标志物与临床反应的相关性

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摘要

Bone marrow mesenchymal stromal cells (BMSCs) have been used to treat acute graft-versus-host disease (GVHD) and other complications following allogeneic hematopoietic stem cell transplantation (SCT). We conducted a phase I trial using third party, early passage BMSCs for patients with steroid-refractory GVHD, tissue injury, or marrow failure following SCT to investigate safety and efficacy. To identify mechanisms of BMSC immunomodulation and tissue repair, patients were serially monitored for plasma GVHD biomarkers, cytokines, and lymphocyte phenotype. Ten subjects were infused a fixed dose of 2 × 106 BMSCs/kg intravenously weekly for three doses. There was no treatment-related toxicity (primary endpoint). Eight subjects were evaluable for response at 4 weeks after the last infusion. Five of the seven patients with steroid-refractory acute GVHD achieved a complete response, two of two patients with tissue injury (pneumomediastinum/pneumothorax) achieved resolution but there was no response in two subjects with delayed marrow failure. Rapid reductions in inflammatory cytokines were observed. Clinical responses correlated with a fall in biomarkers (Reg 3α, CK18, and Elafin) relevant for the site of GVHD or tissue injury. The GVHD complete responders survived significantly longer and had higher baseline absolute lymphocyte and central memory CD4 and CD8 counts. Cytokine changes also segregated with survival. These results confirm that BMSCs are associated with rapid clinical and biomarker responses in GVHD and tissue injury. However, BMSCs were ineffective in patients with prolonged GVHD with lower lymphocyte counts, which suggest that effective GVHD control by BMSCs requires a relatively intact immune system.
机译:骨髓间充质基质细胞(BMSC)已用于治疗同种异体造血干细胞移植(SCT)后的急性移植物抗宿主病(GVHD)和其他并发症。我们进行了I级试验,使用第三方,早期通过的BMSC对类固醇难治性GVHD,组织损伤或SCT后骨髓衰竭的患者进行研究,以研究其安全性和有效性。为了确定BMSC免疫调节和组织修复的机制,对患者的血浆GVHD生物标志物,细胞因子和淋巴细胞表型进行了连续监测。十名受试者每周静脉注射固定剂量的2×106 BMSC / kg,共三剂。没有与治疗有关的毒性(主要终点)。在最后一次输注后第4周评估了8名受试者的反应。七名类固醇难治性急性GVHD患者中有五名获得了完全缓解,两名组织损伤(肺纵隔/气胸)患者中有两名获得了缓解,但两名骨髓衰竭延迟患者中无任何缓解。观察到炎性细胞因子的快速减少。临床反应与与GVHD或组织损伤部位有关的生物标志物(Reg3α,CK18和Elafin)下降有关。 GVHD完全应答者存活时间更长,基线绝对淋巴细胞和中枢记忆CD4和CD8计数更高。细胞因子的变化也与生存分开。这些结果证实,BMSC与GVHD和组织损伤中的快速临床和生物标记反应有关。但是,BMSC对淋巴细胞计数较低的GVHD延长的患者无效,这表明BMSC有效控制GVHD需要相对完整的免疫系统。

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