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优化人脐带来源间充质干细胞在移植物抗宿主病 NSG 小鼠异种移植模型中的治疗效果。

Optimization of the therapeutic efficacy of human umbilical cord blood-mesenchymal stromal cells in an NSG mouse xenograft model of graft-versus-host disease.

机构信息

Biomedical Research Institute, MEDIPOST Co., Ltd., Seoul, Korea.

Department of Pediatrics, Hanyang University Medical Center, Seoul, Korea.

出版信息

Cytotherapy. 2014 Mar;16(3):298-308. doi: 10.1016/j.jcyt.2013.10.012. Epub 2014 Jan 11.

Abstract

BACKGROUND AIMS

Although in vitro studies have demonstrated the immunosuppressive capacity of mesenchymal stromal cells (MSCs), most in vivo studies on graft-versus-host disease (GVHD) have focused on prevention, and the therapeutic effect of MSCs is controversial. Moreover, optimal time intervals for infusing MSCs have not been established.

METHODS

We attempted to evaluate whether human umbilical cord blood-MSCs (hUCB-MSCs) could either prevent or treat GVHD in an NSG mouse xenograft model by injection of MSCs before or after in vivo clearance. Mice were infused with either a single dose or multiple doses of 5 × 10(5) hUCB-MSCs (3- or 7-day intervals) before or after GVHD onset.

RESULTS

Before onset, hUCB-MSCs significantly improved the survival rate only when repeatedly injected at 3-day intervals. In contrast, single or repeated injections after GVHD onset significantly increased the survival rate and effectively attenuated tissue damage and inflammation. Furthermore, the levels of prostaglandin E2 and transforming growth factor-β1 increased significantly, whereas the level of interferon-γ decreased significantly in all MSC treatment groups.

CONCLUSIONS

These data establish the optimal time intervals for preventing GVHD and show that hUCB-MSCs effectively attenuated symptoms and improved survival rate when administered after the onset of GVDH.

摘要

背景目的

尽管体外研究已经证明间充质基质细胞(MSCs)具有免疫抑制能力,但大多数关于移植物抗宿主病(GVHD)的体内研究都集中在预防上,MSCs 的治疗效果存在争议。此外,尚未确定输注 MSCs 的最佳时间间隔。

方法

我们试图通过在体内清除前后注射 MSC 来评估人脐血间充质基质细胞(hUCB-MSCs)是否可以预防或治疗 NSG 小鼠异种移植模型中的 GVHD。在 GVHD 发作之前或之后,用单次或多次剂量的 5×10(5)hUCB-MSCs(3 天或 7 天间隔)输注小鼠。

结果

在发病前,只有在以 3 天间隔重复注射时,hUCB-MSCs 才能显著提高存活率。相比之下,GVHD 发作后单次或多次注射可显著提高存活率,并有效减轻组织损伤和炎症。此外,所有 MSC 治疗组的前列腺素 E2 和转化生长因子-β1 水平显著升高,而干扰素-γ水平显著降低。

结论

这些数据确定了预防 GVHD 的最佳时间间隔,并表明 hUCB-MSCs 在 GVDH 发作后给药时可有效减轻症状并提高存活率。

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