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

被引:113
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
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
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