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The role of programmed cell death ligand-1 (PD-L1/CD274) in the development of graft versus host disease

Authors :
Ali Moshfegh
Heevy Al-Chaqmaqchi
Joachim Lundahl
Sulaiman Al-Hashmi
Mona Fares
Behnam Sadeghi
Manuchehr Abedi-Valugerdi
Moustapha Hassan
Raoul Kuiper
Source :
PLoS ONE, Vol 8, Iss 4, p e60367 (2013), PLoS ONE
Publication Year :
2013
Publisher :
Public Library of Science (PLoS), 2013.

Abstract

Programmed cell death ligand-1 (PD-L1/CD274) is an immunomodulatory molecule involved in cancer and complications of bone marrow transplantation, such as graft rejection and graft-versus-host disease. The present study was designed to assess the dynamic expression of this molecule after hematopoietic stem cell transplantation in relation to acute graft-versus-host disease. Female BALB/c mice were conditioned with busulfan and cyclophosphamide and transplanted with either syngeneic or allogeneic (male C57BL/6 mice) bone marrow and splenic cells. The expression of PD-L1 was evaluated at different time points employing qPCR, western blot and immunohistochemistry. Allogeneic- but not syngeneic-transplanted animals exhibited a marked up-regulation of PD-L1 expression in the muscle and kidney, but not the liver, at days 5 and 7 post transplantation. In mice transplanted with allogeneic bone marrow cells, the enhanced expression of PD-L1 was associated with high serum levels of IFNγ and TNFα at corresponding intervals. Our findings demonstrate that PD-L1 is differently induced and expressed after allogeneic transplantation than it is after syngeneic transplantation, and that it is in favor of target rather than non-target organs at the early stages of acute graft-versus-host disease. This is the first study to correlate the dynamics of PD-L1 at the gene-, protein- and activity levels with the early development of acute graft-versus-host disease. Our results suggest that the higher expression of PD-L1 in the muscle and kidney (non-target tissues) plays a protective role in skeletal muscle during acute graft-versus-host disease.

Details

Language :
English
ISSN :
19326203
Volume :
8
Issue :
4
Database :
OpenAIRE
Journal :
PLoS ONE
Accession number :
edsair.doi.dedup.....344bc473b4048e0e934fec5aafda527c