Immunoregulatory effects of multipotent adult progenitor cells in a porcine ex vivo lung perfusion model

Bibliographic Details
Title: Immunoregulatory effects of multipotent adult progenitor cells in a porcine ex vivo lung perfusion model
Authors: An Martens, Sofie Ordies, Bart M. Vanaudenaerde, Stijn E. Verleden, Robin Vos, Dirk E. Van Raemdonck, Geert M. Verleden, Valerie D. Roobrouck, Sandra Claes, Dominique Schols, Eric Verbeken, Catherine M. Verfaillie, Arne P. Neyrinck
Source: Stem Cell Research & Therapy, Vol 8, Iss 1, Pp 1-9 (2017)
Publisher Information: BMC, 2017.
Publication Year: 2017
Collection: LCC:Medicine (General)
LCC:Biochemistry
Subject Terms: Multipotent adult progenitor cell, Ex vivo lung perfusion, Immunomodulation, Ischemia-reperfusion injury, Porcine, Immunoregulation, Medicine (General), R5-920, Biochemistry, QD415-436
More Details: Abstract Background Primary graft dysfunction (PGD) is considered to be the end result of an inflammatory response targeting the new lung allograft after transplant. Previous research has indicated that MAPC cell therapy might attenuate this injury by its paracrine effects on the pro-/anti-inflammatory balance. This study aims to investigate the immunoregulatory capacities of MAPC cells in PGD when administered in the airways. Methods Lungs of domestic pigs (n = 6/group) were subjected to 90 minutes of warm ischemia. Lungs were cold flushed, cannulated on ice and placed on EVLP for 6 hours. At the start of EVLP, 40 ml of an albumin-plasmalyte mixture was distributed in the airways (CONTR group). In the MAPC cell group, 150 million MAPC cells (ReGenesys/Athersys, Cleveland, OH, USA) were added to this mixture. At the end of EVLP, a physiological evaluation (pulmonary vascular resistance, lung compliance, PaO2/FiO2), wet-to-dry weight ratio (W/D) sampling and a multiplex analysis of bronchoalveolar lavage (BAL) (2 × 30 ml) was performed. Results Pulmonary vascular resistance, lung compliance, PaO2/FiO2 and W/D were not statistically different at the end of EVLP between both groups. BAL neutrophilia was significantly reduced in the MAPC cell group. Moreover, there was a significant decrease in TNF-α, IL-1β and IFN-γ in the BAL, but not in IFN-α; whereas IL-4, IL-10 and IL-8 were below the detection limit. Conclusions Although no physiologic effect of MAPC cell distribution in the airways was detected during EVLP, we observed a reduction in pro-inflammatory cytokines and neutrophils in BAL in the MAPC cell group. This effect on the innate immune system might play an important role in critically modifying the process of PGD after transplantation. Further experiments will have to elucidate the immunoregulatory effect of MAPC cell administration on graft function after transplantation.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1757-6512
Relation: http://link.springer.com/article/10.1186/s13287-017-0603-5; https://doaj.org/toc/1757-6512
DOI: 10.1186/s13287-017-0603-5
Access URL: https://doaj.org/article/fe62859529ac4877b3e2018cf3483b36
Accession Number: edsdoj.fe62859529ac4877b3e2018cf3483b36
Database: Directory of Open Access Journals
More Details
ISSN:17576512
DOI:10.1186/s13287-017-0603-5
Published in:Stem Cell Research & Therapy
Language:English