Safety of Stromal Vascular Fraction Cell Therapy for Chronic Kidney Disease of Unknown Cause (Mesoamerican Nephropathy)

被引:1
|
作者
Carstens, Michael H. [1 ,2 ,3 ]
Garcia, Nelson [4 ,5 ]
Mandayam, Sreedhar [6 ]
Workeneh, Biruh [6 ]
Pastora, Indiana [4 ]
Calderon, Carlos [7 ]
Bertram, Kenneth A. [3 ]
Correa, Diego [8 ,9 ,10 ,11 ]
机构
[1] Univ Nacl Autonoma Nicaragua, Dept Surg, Leon, Spain
[2] Hosp Vivian Pellas, Managua, Nicaragua
[3] Wake Forest Univ, Inst Regenerat Med, Winston Salem, NC 27101 USA
[4] Univ Nacl Autonoma Nicaragua, Dept Med, Leon, Nicaragua
[5] Minist Salud, Nephrol Sect, Managua, Nicaragua
[6] Univ Texas MD Anderson Canc Ctr, Dept Nephrol, Houston, TX 77030 USA
[7] Hosp San Juan Dios, Dept Cardiol, San Jose, Costa Rica
[8] Univ Miami, Miller Sch Med, Diabet Res Inst, Miami, FL USA
[9] Univ Miami, Miller Sch Med, Cell Transplant Ctr, Miami, FL USA
[10] Diabet Res Inst Federat, Hollywood, FL 33021 USA
[11] Cell & Gene Therapy Ctr Excellence, IQVIA, Durham, NC USA
关键词
chronic kidney disease of unknown cause (CKDu); Mesoamerican nephropathy; neovascularization; stromal vascular fraction (SVF); cell-based therapy; safety; PATHOLOGY;
D O I
10.1093/stcltm/szac080
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Chronic kidney disease of unknown cause (CKDu), also known as Mesoamerican nephropathy, typically presents as an ischemic nephropathy with chronic tubulointerstitial fibrosis in normotensive patients, rapidly progressing to kidney failure. In this first-in-human, open-label, safety study, we followed 18 patients with CKDu (stages 3-5) for 36 months after receiving a single infusion of angiogenic/anti-fibrotic autologous adipose-derived stromal vascular fraction (SVF) cells into their kidneys bilaterally via renal artery catheterization. SVF therapy was safe and well tolerated. There were no SVF-related serious adverse events and no procedural complications. Color Doppler evaluation at 2 months demonstrated increased perfusion to the interlobar and/or arcuate artery levels in each kidney evaluated (36/36) with a reduction in resistance index at the hilar artery (35/36) kidneys. Beyond 12 months, patients with initial eGFR <30 mL/minute/1.73 m(2) deteriorated, whereas those >= 30 mL/minute/1.73 m(2) further sustained their renal function, suggesting a possible renal protective effect in that group.
引用
收藏
页码:7 / 16
页数:10
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