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在脐带血移植后,将扩增的脐带血T细胞用作供体淋巴细胞输注。

Expanded umbilical cord blood T cells used as donor lymphocyte infusions after umbilical cord blood transplantation.

作者信息

Berglund Sofia, Gertow Jens, Uhlin Michael, Mattsson Jonas

机构信息

Center for Allogeneic Stem Cell Transplantation, Karolinska University Hospital, Stockholm, Sweden; Department of Laboratory Medicine, Division of Therapeutic Immunology, Karolinska Institutet, Stockholm, Sweden.

Department of Laboratory Medicine, Division of Therapeutic Immunology, Karolinska Institutet, Stockholm, Sweden.

出版信息

Cytotherapy. 2014 Nov;16(11):1528-1536. doi: 10.1016/j.jcyt.2014.08.001. Epub 2014 Sep 16.

Abstract

BACKGROUND

Umbilical cord blood (UCB) is an alternative graft source for hematopoietic stem cell transplantation and has been shown to give results comparable to transplantation with other stem cell sources. Donor lymphocyte infusion (DLI) is an effective treatment for relapsed malignancies after hematopoietic stem cell transplantation. However, DLI is not available after UCB transplantation.

METHODS

In this study, in vitro-cultured T cells from the UCB graft were explored as an alternative to conventional DLI. The main aim was to study the safety of the cultured UCB T cells used as DLI because such cell preparations have not been used in this context previously. We also assessed potential benefits of the treatment.

RESULTS

The cultured UCB T cells (UCB DLI) were given to 4 patients with mixed chimerism (n = 2), minimal residual disease (n = 1) and graft failure (n = 1). No adverse reactions were seen at transfusion. Three of the patients did not show any signs of graft-versus-host disease (GVHD) after UCB DLI, but GVHD could not be excluded in the last patient. In the patient with minimal residual disease treated with UCB DLI, the malignant cell clone was detectable shortly before infusion but undetectable at treatment and for 3 months after infusion. In 1 patient with mixed chimerism, the percentage of recipient cells decreased in temporal association with UCB DLI treatment.

CONCLUSIONS

We saw no certain adverse effects of treatment with UCB DLI. Events that could indicate possible benefits were seen but with no certain causal association with the treatment.

摘要

背景

脐带血(UCB)是造血干细胞移植的一种替代移植物来源,已显示其结果与其他干细胞来源的移植相当。供体淋巴细胞输注(DLI)是造血干细胞移植后复发恶性肿瘤的有效治疗方法。然而,UCB移植后无法进行DLI。

方法

在本研究中,探索将UCB移植物中体外培养的T细胞作为传统DLI的替代方法。主要目的是研究用作DLI的培养UCB T细胞的安全性,因为此类细胞制剂此前尚未在此背景下使用。我们还评估了该治疗的潜在益处。

结果

将培养的UCB T细胞(UCB DLI)给予4例患者,分别为混合嵌合体(n = 2)、微小残留病(n = 1)和移植物失败(n = 1)。输血时未观察到不良反应。3例患者在接受UCB DLI后未出现任何移植物抗宿主病(GVHD)迹象,但最后1例患者不能排除GVHD。在接受UCB DLI治疗的微小残留病患者中,恶性细胞克隆在输注前不久可检测到,但在治疗时及输注后3个月未检测到。在1例混合嵌合体患者中,受体细胞百分比随UCB DLI治疗呈时间相关性下降。

结论

我们未发现UCB DLI治疗有确切的不良反应。观察到可能提示益处的事件,但与治疗无确切因果关系。

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