The Promise of Mesenchymal Stem Cell Therapy for Diabetic Kidney Disease

被引:43
|
作者
Griffin, Tomas P. [1 ,2 ]
Martin, William Patrick [1 ,2 ]
Islam, Nahidul [1 ]
O'Brien, Timothy [1 ,2 ]
Griffin, Matthew D. [1 ,3 ]
机构
[1] Natl Univ Ireland, Coll Med Nursing & Hlth Sci, Sch Med, Regenerat Med Inst REMEDI,CURAM Ctr Res Med Devic, Galway, Ireland
[2] Saolta Univ Hlth Grp, Ctr Diabet Endocrinol & Metab, Galway Univ Hosp, Galway, Ireland
[3] Saolta Univ Hlth Grp, Galway Univ Hosp, Serv Nephrol, Galway, Ireland
基金
爱尔兰科学基金会;
关键词
Diabetes mellitus; Diabetic nephropathy; Stem cells; Mesenchymal stem cells; Inflammation; ENDOTHELIAL GROWTH-FACTOR; AMELIORATES GLOMERULAR INJURY; URINARY ADIPONECTIN EXCRETION; ALL-CAUSE MORTALITY; REGULATORY T-CELLS; TNF RECEPTORS 1; RENAL-DISEASE; SERUM ADIPONECTIN; TUBULAR MARKERS; STROMAL CELLS;
D O I
10.1007/s11892-016-0734-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Diabetes mellitus (DM) commonly leads to progressive chronic kidney disease despite current best medical practice. The pathogenesis of diabetic kidney disease (DKD) involves a complex network of primary and secondary mechanisms with both intra-renal and systemic components. Apart from inhibition of the renin angiotensin aldosterone system, targeting individual pathogenic mediators with drug therapy has not, thus far, been proven to have high clinical value. Stem or progenitor cell therapies offer an alternative strategy for modulating complex disease processes through suppressing multiple pathogenic pathways and promoting pro-regenerative mechanisms. Mesenchymal stem cells (MSCs) have shown particular promise based on their accessibility from adult tissues and their diverse mechanisms of action including secretion of paracrine anti-inflammatory and cytoprotective factors. In this review, the progress toward clinical translation of MSC therapy for DKD is critically evaluated. Results from animal models suggest distinct potential for systemic MSC infusion to favourably modulate DKD progression. However, only a few early phase clinical trials have been initiated and efficacy in humans remains to be proven. Key knowledge gaps and research opportunities exist in this field. These include the need to gain greater understanding of in vivo mechanism of action, to identify quantifiable biomarkers of response to therapy and to define the optimal source, dose and timing of MSC administration. Given the rising prevalence of DM and DKD worldwide, continued progress toward harnessing the inherent regenerative functions of MSCs and other progenitor cells for even a subset of those affected has potential for profound societal benefits.
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页数:14
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