Impact of donor hematopoietic cells mobilized with G-CSF and plerixafor on murine acute graft-versus-host-disease
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Titre | Impact of donor hematopoietic cells mobilized with G-CSF and plerixafor on murine acute graft-versus-host-disease |
Type de publication | Journal Article |
Year of Publication | 2015 |
Auteurs | Arbez J, Saas P, Lamarthee B, Malard F, Couturier M, Mohty M, Gaugler B |
Journal | CYTOTHERAPY |
Volume | 17 |
Pagination | 948-955 |
Date Published | JUL |
Type of Article | Article |
ISSN | 1465-3249 |
Mots-clés | acute GVHD, dendritic cells, immune effectors, mobilization, peripheral blood stem cells, plerixafor |
Résumé | Background aims. This study aimed to characterize the immune effectors contained in the grafts from donor mice mobilized by granulocyte colony-stimulating factor (G-CSF) and plerixafor and to evaluate their impact on the development of acute graft-versus-host-disease (aGVHD). Methods. Mobilization was done with G-CSF alone or G-CSF plus plerixafor (G+P). Results. In grafts collected after G+P mobilization, we observed a significantly higher proportion of c-kit(+)Sca-1(+) hematopoietic stem cells compared with G-CSF. A significant increase in the percentage of plasmacytoid dendritic cells was detected in the G+P graft compared with G-CSF graft. We also studied the ability of stem cell grafts mobilized with G+P to induce GVHD in a mouse model. We observed higher mortality (P < 0.001) associated with increased aGVHD clinical score (P < 0.0001) as well as higher pathology score in the intestine of mice receiving G+P as compared with G-CSF grafts (P < 0.001). Moreover, the exacerbated aGVHD severity was associated with upregulation of CCR6 expression on both CD4(+) and CD8(+) T cells from the G+P grafts, as well as on T cells from mice transplanted with G+P grafts. Conclusions. In conclusion, we showed that grafts mobilized with G+P exhibited functional features different from those mobilized with G-CSF alone, which increase the severity of aGVHD in the recipients. |
DOI | 10.1016/j.jcyt.2015.02.009 |