Article (Scientific journals)
Azacytidine prevents experimental xenogeneic graft-versus-host disease without abrogating graft-versus-leukemia effects
Ehx, Grégory; Fransolet, Gilles; De Leval, Laurence et al.
2017In Oncoimmunology, p. 6:e1314425
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Keywords :
Azacytidine; graft-vs.-host disease; graft-vs.-leukemia effect; NOD-scid IL-2Rgnull; regulatory T cells
Abstract :
[en] The demethylating agent 5-azacytidine (AZA) has proven its efficacy as treatment for myelodysplastic syndrome and acute myeloid leukemia. In addition, AZA can demethylate FOXP3 intron 1 (FOXP3i1) leading to the generation of regulatory T cells (Treg). Here, we investigated the impact of AZA on xenogeneic graft-versus-host disease (xGVHD) and graft-versus-leukemia effects in a humanized murine model of transplantation (human PBMCs-infused NSG mice), and described the impact of the drug on human T cells in vivo. We observed that AZA improved both survival and xGVHD scores. Further, AZA significantly decreased human T-cell proliferation as well as IFN-γ and TNF-α serum levels, and reduced the expression of GRANZYME B and PERFORIN 1 by cytotoxic T cells. In addition, AZA significantly increased Treg frequency through hypomethylation of FOXP3i1 as well as increased Treg proliferation. The later was subsequent to higher STAT5 signaling in Treg from AZA-treated mice, which resulted from higher IL-2 secretion by conventional T cells from AZA-treated mice itself secondary to demethylation of the IL-2 gene promoter by AZA. Importantly, Tregs harvested from AZA-treated mice were suppressive and stable over time since they persisted at high frequency in secondary transplant experiments. Finally, graft-versus-leukemia effects (assessed by growth inhibition of THP-1 cells, transfected to express the luciferase gene) were not abrogated by AZA. In summary, our data demonstrate that AZA prevents xGVHD without abrogating graft-versus-leukemia effects. These findings could serve of basis for further studies of GVHD prevention by AZA in acute myeloid leukemia patients offered an allogeneic transplantation.
Research Center/Unit :
GIGA-I3 - Giga-Infection, Immunity and Inflammation - ULiège
Disciplines :
Biochemistry, biophysics & molecular biology
Author, co-author :
Ehx, Grégory  ;  Université de Liège > GIGA-R : Hématologie
Fransolet, Gilles ;  Université de Liège > GIGA-R : Hématologie
De Leval, Laurence;  CHU Vaudois > Institute of Pathology
D'Hondt, Stéphanie;  Université Catholique de Louvain - UCL > Institut De Duve
Lucas, Sophie;  Université Catholique de Louvain - UCL > Institut De Duve
Hannon, Muriel ;  Université de Liège > GIGA-R : Hématologie
Delens, Loïc ;  Université de Liège > GIGA-R : Hématologie
DUBOIS, Sophie ;  Centre Hospitalier Universitaire de Liège - CHU > Service d'hématologie clinique
Drion, Pierre ;  Université de Liège > Département des sciences biomédicales et précliniques > GIGA-R:Méth. expér.des anim. de labo et éth. en expér. anim.
Beguin, Yves  ;  Université de Liège > GIGA-R : Hématologie
Humblet-Baron, Stéphanie;  KU Leuven > Department of Microbiology and Immunology
Baron, Frédéric  ;  Université de Liège > GIGA-R : Hématologie
Language :
English
Title :
Azacytidine prevents experimental xenogeneic graft-versus-host disease without abrogating graft-versus-leukemia effects
Publication date :
2017
Journal title :
Oncoimmunology
ISSN :
2162-4011
eISSN :
2162-402X
Publisher :
Taylor & Francis, Philadelphia, United States - Pennsylvania
Pages :
6:e1314425
Peer reviewed :
Peer Reviewed verified by ORBi
Funders :
F.R.S.-FNRS - Fonds de la Recherche Scientifique
Available on ORBi :
since 27 April 2017

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