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间充质干细胞疗法促进角膜移植存活:现状与临床转化途径

Mesenchymal stem cell therapy to promote corneal allograft survival: current status and pathway to clinical translation.

作者信息

Murphy Nick, Lynch Kevin, Lohan Paul, Treacy Oliver, Ritter Thomas

机构信息

aCollege of Medicine, Nursing and Health Sciences, Regenerative Medicine Institute, National University of Ireland, Galway, Ireland *Both authors contributed equally to this manuscript.

出版信息

Curr Opin Organ Transplant. 2016 Dec;21(6):559-567. doi: 10.1097/MOT.0000000000000360.

Abstract

PURPOSE OF REVIEW

This article reviews the literature on the therapeutic potential of mesenchymal stem cells (MSCs) to prolong corneal allograft survival.

RECENT FINDINGS

To date, only small numbers studies have investigated the MSC ability to modulate corneal allograft survival. Most reports have shown positive results, which is encouraging, however as different MSC-application strategies (time point of injection, cell number/number of injections, route of injection, MSC source, MSC licensing) have been employed in various animal models it is difficult to compare and validate the results. The MSC ability to promote graft survival has been attributed to their modulation of the recipient immune system, altering the Th1/Th2 balance, expanding Foxp3 regulatory T cells, polarizing macrophages and inhibiting intra-graft infiltration of antigen presenting cells. More in depth analysis is required to elucidate the mechanism of MSC-immunomodulation in vivo.

SUMMARY

MSCs have shown the potential to modulate corneal allograft rejection in various models using MSCs from different species. In particular for high-risk patients with poor prognosis MSC therapy might be a promising approach to promote corneal allograft survival. First-in-man clinical trials with MSC will hopefully shed new light on MSC-mediated immunomodulation in vivo and contribute to the restoration of vision in patients receiving corneal allografts.

摘要

综述目的

本文综述了间充质干细胞(MSCs)在延长角膜移植存活方面的治疗潜力的相关文献。

最新研究成果

迄今为止,仅有少数研究调查了MSCs调节角膜移植存活的能力。大多数报告显示出阳性结果,这令人鼓舞,然而,由于在各种动物模型中采用了不同的MSCs应用策略(注射时间点、细胞数量/注射次数、注射途径、MSCs来源、MSCs许可),因此难以比较和验证结果。MSCs促进移植存活的能力归因于它们对受体免疫系统的调节,改变Th1/Th2平衡,扩增Foxp3调节性T细胞,使巨噬细胞极化以及抑制抗原呈递细胞在移植组织内的浸润。需要更深入的分析来阐明MSCs在体内免疫调节的机制。

总结

在各种模型中,使用来自不同物种的MSCs已显示出调节角膜移植排斥反应的潜力。特别是对于预后不良的高风险患者,MSCs治疗可能是促进角膜移植存活的一种有前景的方法。MSCs的首次人体临床试验有望为体内MSCs介导的免疫调节提供新的见解,并有助于接受角膜移植患者的视力恢复。

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