Allogeneic Mesenchymal Precursor Cells (MPC) in Diabetic Nephropathy: A Randomized, Placebo-controlled, Dose Escalation Study

被引:108
作者
Packham, David K. [1 ,2 ]
Fraser, Ian R. [3 ]
Kerr, Peter G. [4 ,5 ]
Segal, Karen R. [6 ]
机构
[1] Melbourne Renal Res Grp, Melbourne, Vic, Australia
[2] Univ Melbourne, Dept Med, Melbourne, Vic, Australia
[3] Epworth Med Ctr, Richmond, Vic, Australia
[4] Monash Med Ctr, Clayton, Vic, Australia
[5] Monash Univ, Clayton, Vic, Australia
[6] Mesoblast Inc, New York, NY USA
来源
EBIOMEDICINE | 2016年 / 12卷
关键词
Mesenchymal precursor cells; Diabetic nephropathy; Stem cell; Inflammation; Glomerular filtration rate; KIDNEY-DISEASE; THERAPY; MECHANISMS; RATIONALE; SAFETY; MSCS;
D O I
10.1016/j.ebiom.2016.09.011
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Diabetic nephropathy is the most common cause of end stage renal failure. We assessed the safety, tolerability, and explored therapeutic effects of adult allogeneic bone-marrow derived mesenchymal precursor cells (MPC) in patients with moderate to severe diabetic nephropathy. Methods: Multicenter, randomized, double-blind, dose-escalating, sequential, placebo-controlled trial assessing a single intravenous (IV) infusion of allogeneic MPC (United States adopted name: rexlemestrocel-L) 150 x 10(6) (n =10), 300 x 10(6) (n=10) or placebo (n=10) in adults with diabetic nephropathy with an estimated glomerular filtration rate (eGFR) 20-50 ml/min/1.73 m(2). Thirty patients at three Australian centers were enrolled between July 2013 and June 2014 and randomized 2: 1, in two sequential dose cohorts, to receive rexlemestrocel-L or placebo. Study duration was 60 weeks. Primary endpoint was safety and tolerability. Primary exploratory efficacy endpoint was change from baseline in eGFR and directly measured GFR by Tc-99-DTPA plasma clearance (mGFR) at 12 weeks post-infusion. The trial was registered on ClinicalTrials.gov (NCT01843387). Findings: All patients completed the study and were included in analyses applied to the intention to treat population. There were no acute adverse events (AEs) associated with infusion and no treatment-related AEs or serious AEs were deemed treatment-related by investigators. No patients developed persistent donor specific anti-HLA antibodies. Relative to placebo, a single IV rexlemestrocel-L infusion showed trends of stabilizing or improving eGFR and mGFR at week 12. The adjusted least squares mean (LSM +/- SE) differences from placebo in changes from baseline at 12 weeks in the rexlemestrocel-L groups were 4.4 +/- 2.16 and 1.6 +/- 2.15 ml/min/1.73 m(2) for eGFR and 4.1 +/- 2.75 and 3.9 +/- 2.75 for mGFR for the 150 x 10(6) and 300 x 10(6) cell groups, respectively. Interpretation: This study demonstrates the safety of rexlemestrocel-L in diabetic nephropathy with suggestive effects on renal function to be confirmed in larger, appropriately powered trials. (C) 2016 The Authors. Published by Elsevier B.V.
引用
收藏
页码:263 / 269
页数:7
相关论文
共 27 条
[1]  
[Anonymous], 2010, COMM TERM CRIT ADV E
[2]   Effects of losartan on renal and cardiovascular outcomes in patients with type 2 diabetes and nephropathy [J].
Brenner, BM ;
Cooper, ME ;
de Zeeuw, D ;
Keane, WF ;
Mitch, WE ;
Parving, HH ;
Remuzzi, G ;
Snapinn, SM ;
Zhang, ZX ;
Shahinfar, S .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 345 (12) :861-869
[3]   Rationale of Mesenchymal Stem Cell Therapy in Kidney Injury [J].
Cantaluppi, Vincenzo ;
Biancone, Luigi ;
Quercia, Alessandro ;
Deregibus, Maria Chiara ;
Segoloni, Giuseppe ;
Camussi, Giovanni .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2013, 61 (02) :300-309
[4]   A novel monoclonal antibody (STRO-3) identifies an isoform of tissue nonspecific alkaline phosphatase expressed by multipotent bone marrow stromal stem cells [J].
Gronthos, Stan ;
Fitter, Stephen ;
Diamond, Peter ;
Simmons, Paul J. ;
Itescu, Silviu ;
Zannettin, Andrew C. W. .
STEM CELLS AND DEVELOPMENT, 2007, 16 (06) :953-963
[5]   Challenges and opportunities for stem cell therapy in patients with chronic kidney disease [J].
Hickson, LaTonya J. ;
Eirin, Alfonso ;
Lerman, Lilach O. .
KIDNEY INTERNATIONAL, 2016, 89 (04) :767-778
[6]  
Kidney disease: improving global outcomes (KDIGO) CKD work group, 2013, Kidney Int, V3, P1, DOI [DOI 10.1038/KISUP.2012.73, 10.1038/kisup.2012.73]
[7]   Mesenchymal stem cell-educated macrophages: A novel type of alternatively activated macrophages [J].
Kim, Jaehyup ;
Hematti, Peiman .
EXPERIMENTAL HEMATOLOGY, 2009, 37 (12) :1445-1453
[8]   A New Equation to Estimate Glomerular Filtration Rate [J].
Levey, Andrew S. ;
Stevens, Lesley A. ;
Schmid, Christopher H. ;
Zhang, Yaping ;
Castro, Alejandro F., III ;
Feldman, Harold I. ;
Kusek, John W. ;
Eggers, Paul ;
Van Lente, Frederick ;
Greene, Tom ;
Coresh, Josef .
ANNALS OF INTERNAL MEDICINE, 2009, 150 (09) :604-612
[9]   A more accurate method to estimate glomerular filtration rate from serum creatinine: A new prediction equation [J].
Levey, AS ;
Bosch, JP ;
Lewis, JB ;
Greene, T ;
Rogers, N ;
Roth, D .
ANNALS OF INTERNAL MEDICINE, 1999, 130 (06) :461-+
[10]   Renoprotective effect of the angiotensin-receptor antagonist irbesartan in patients with nephropathy due to type 2 diabetes [J].
Lewis, EJ ;
Hunsicker, LG ;
Clarke, WR ;
Berl, T ;
Pohl, MA ;
Lewis, JB ;
Ritz, E ;
Atkins, RC ;
Rohde, R ;
Raz, I .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 345 (12) :851-860