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Adipose tissue-derived mesenchymal stromal cells as part of therapy for chronic graft-versus-host disease: A phase I/II study

机译:脂肪组织衍生的间充质基质细胞作为慢性移植物 - 与宿主疾病的一部分:I / II期研究

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Background aims. Despite the efficacy of allogeneic hematopoietic stem cell transplantation (allo-HSCT), the procedure is still associated with high toxicity in patients with refractory graft-versus-host disease (GvHD). Mesenchymal stromal cells (MSCs) are a new mode of therapy in the context of allo-HSCT. The objective of this study was to evaluate the safety and feasibility of the use of adipose tissue-derived MSCs (AT-MSCs) in patients with chronic GvHD. Methods. Fourteen patients with moderate (n = 7) or severe (n = 7) chronic GvHD received 1 x 10(6)/kg (group A, n = 9) or 3 x 10(6)/kg (group B, n = 5) AT-MSCs with cyclosporine and prednisone as first-line therapy. Results. Ten of the 14 patients were able to continue under the protocol: 80% were in complete remission, and 100% were off of steroids at week 56. The remaining 4 patients either worsened from chronic GvHD (n = 3) or abandoned the study (n = 1). At the end of the study, 11 of 14 patients are alive (overall survival 71.4%, median survival of 45.3 weeks). No suspected unexpected serious adverse reactions occurred during the trial. Neither relapse of underlying disease nor mortality due to infection was observed in this cohort. Biological studies showed increased CD19, CD4 and tumor necrosis factor-alpha with a temporary decrease in natural killer cells. Discussion. AT-MSCs, in combination with immunosuppressive therapy, may be considered feasible and safe and likely would have an impact on the course of chronic GvHD. More studies are warranted to understand the potential benefits of AT-MSCs in these patients.
机译:背景目标。尽管同种异体造血干细胞移植(ALLO-HSCT)有效,但该程序仍然与难治性移植患者与宿主疾病(GVHD)患者的高毒性有关。间充质基质细胞(MSCs)是Allo-HSCT的背景下的一种新的治疗模式。本研究的目的是评估在慢性GVHD患者中使用脂肪组织衍生的MSCs(AT-MSCs)的安全性和可行性。方法。 14例中度(n = 7)或严重(n = 7)慢性GVHD接受1×10(6)/ kg(A,n = 9)或3×10(6)/ kg(B,n = 5)具有环孢菌素和泼尼松的AT-MSCs作为一线疗法。结果。 14名患者中的十个能够继续在方案下继续:80%在完全缓解中,100%在第56周的类固醇中脱离。剩余的4名患者无论是从慢性GVHD(n = 3)恶化还是废弃的研究( n = 1)。在研究结束时,14名患者中的11名中有11名(整体生存71.4%,中位存活率为45.3周)。在审判期间没有疑似意外的严重不良反应。在该队列中观察到由于感染引起的潜在疾病的复发和死亡率。生物学研究显示CD19,CD4和肿瘤坏死因子-α增加,临时降低自然杀伤细胞。讨论。 AT-MSCs与免疫抑制治疗组合,可能被认为是可行和安全的,并且可能会对慢性GVHD的过程产生影响。需要更多的研究来了解这些患者在MSC的潜在益处。

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