| Literature DB >> 27740636 |
M-T Rubio1,2,3,4,5, M Bouillié1,5, N Bouazza6, T Coman1,5, H Trebeden-Nègre7, A Gomez2,3,4, F Suarez1,5,8, D Sibon1,8, A Brignier9, E Paubelle1,5,8, S Nguyen-Khoc10, M Cavazzana5,11,12, O Lantz13,14, M Mohty2,3,4, S Urien6,15, O Hermine1,5,8.
Abstract
Clinically useful pre-transplant predictive factors of acute graft-versus-host-disease (aGVHD) after allogeneic hematopoietic stem cell transplantation (allo-SCT) are lacking. We prospectively analyzed HSC graft content in CD34+, NK, conventional T, regulatory T and invariant natural killer T (iNKT) cells in 117 adult patients before allo-SCT. Results were correlated with occurrence of aGVHD and relapse. In univariate analysis, iNKT cells were the only graft cell populations associated with occurrence of aGVHD. In multivariate analysis, CD4- iNKT/T cell frequency could predict grade II-IV aGVHD in bone marrow and peripheral blood stem cell (PBSC) grafts, while CD4- iNKT expansion capacity was predictive in PBSC grafts. Receiver operating characteristic analyses determined the CD4- iNKT expansion factor as the best predictive factor of aGVHD. Incidence of grade II-IV aGVHD was reduced in patients receiving a graft with an expansion factor above versus below 6.83 (9.7 vs 80%, P<0.0001), while relapse incidence at two years was similar (P=0.5).The test reached 94% sensitivity and 100% specificity in the subgroup of patients transplanted with human leukocyte antigen 10/10 PBSCs without active disease. Analysis of this CD4- iNKT expansion capacity test may represent the first diagnostic tool allowing selection of the best donor to avoid severe aGVHD with preserved graft-versus-leukemia effect after peripheral blood allo-SCT.Entities:
Mesh:
Year: 2016 PMID: 27740636 DOI: 10.1038/leu.2016.281
Source DB: PubMed Journal: Leukemia ISSN: 0887-6924 Impact factor: 11.528