TY - JOUR
T1 - Adipose tissue-derived mesenchymal stromal cells in patients with chronic kidney disease
T2 - A pilot study assessing safety and clinical feasibility
AU - Villanueva, Sandra
AU - González, Fernando
AU - Lorca, Eduardo
AU - Tapia, Andrés
AU - Valentina López, G.
AU - Strodthoff, Rocío
AU - Fajre, Francisca
AU - Carreño, Juan E.
AU - Valjalo, Ricardo
AU - Vergara, César
AU - Lecanda, Manuel
AU - Bartolucci, Jorge
AU - Figueroa, Fernando E.
AU - Khoury, Maroun
N1 - Funding Information:
This work was supported by Cells for Cells (C4C).
Publisher Copyright:
© 2019 by The Korean Society of Nephrology. All rights reserved.
PY - 2019
Y1 - 2019
N2 - Background: Chronic kidney disease (CKD) is a growing public health concern, and available treatments are insufficient in limiting disease progression. New strategies, including regenerative cell-based therapies, have emerged as therapeutic alternatives. Results from several groups, including our own, have reported evidence of a supportive role for mesenchymal stromal cells (MSCs) in functional recovery and prevention of tissue damage in murine models of CKD. Prompted by these data, an open pilot study was conducted to assess the safety and efficacy of a single injection of autologous adipose tissue-derived MSCs (AT-MSCs) for treatment of CKD. Methods: AT-MSCs were infused intravenously into six CKD patients at a dose of 1 million cells/kg. Patients were stabilized and followed for one year prior to MSC infusion and one year following infusion. Results: No patients presented with adverse effects. Statistically significant improvement in urinary protein excretion was observed in AT-MSCs transplanted patients, from a median of 0.75 g/day (range, 0.15-9.57) at baseline to 0.54 g/day (range, 0.01-2.66) at month 12 (P = 0.046). The glomerular filtration rate was not significantly decreased post-infusion of AT-MSCs. Conclusion: Findings from this pilot study demonstrate that intravenous infusion of autologous expanded AT-MSCs into CKD patients was not associated with adverse effects and could benefit patients already undergoing standard medical treatment.
AB - Background: Chronic kidney disease (CKD) is a growing public health concern, and available treatments are insufficient in limiting disease progression. New strategies, including regenerative cell-based therapies, have emerged as therapeutic alternatives. Results from several groups, including our own, have reported evidence of a supportive role for mesenchymal stromal cells (MSCs) in functional recovery and prevention of tissue damage in murine models of CKD. Prompted by these data, an open pilot study was conducted to assess the safety and efficacy of a single injection of autologous adipose tissue-derived MSCs (AT-MSCs) for treatment of CKD. Methods: AT-MSCs were infused intravenously into six CKD patients at a dose of 1 million cells/kg. Patients were stabilized and followed for one year prior to MSC infusion and one year following infusion. Results: No patients presented with adverse effects. Statistically significant improvement in urinary protein excretion was observed in AT-MSCs transplanted patients, from a median of 0.75 g/day (range, 0.15-9.57) at baseline to 0.54 g/day (range, 0.01-2.66) at month 12 (P = 0.046). The glomerular filtration rate was not significantly decreased post-infusion of AT-MSCs. Conclusion: Findings from this pilot study demonstrate that intravenous infusion of autologous expanded AT-MSCs into CKD patients was not associated with adverse effects and could benefit patients already undergoing standard medical treatment.
KW - Adipose tissue-derived mesenchymal stromal cells
KW - Chronic kidney disease
KW - Mesenchymal stromal cell transplantation
KW - Proteinuria
KW - Stem cells
KW - Adipose tissue-derived mesenchymal stromal cells
KW - Chronic kidney disease
KW - Mesenchymal stromal cell transplantation
KW - Proteinuria
KW - Stem cells
UR - http://www.scopus.com/inward/record.url?scp=85069540737&partnerID=8YFLogxK
U2 - 10.23876/j.krcp.18.0139
DO - 10.23876/j.krcp.18.0139
M3 - Article
AN - SCOPUS:85069540737
SN - 2211-9132
VL - 38
SP - 176
EP - 185
JO - Kidney Research and Clinical Practice
JF - Kidney Research and Clinical Practice
IS - 2
ER -