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Cytotoxic T-Lymphocyte Antigen-4 Single Nucleotide Polymorphisms Are Not Associated with Outcomes after Unrelated Donor Transplantation: A Center for International Blood and Marrow Transplant Research Analysis
Affiliation:1. Section of Hematology and Stem Cell Transplantation, Vanderbilt-Ingram Cancer Center, Nashville, Tennessee;2. Division of Biostatistics, Medical College of Wisconsin, Milwaukee, Wisconsin;3. Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington;4. Center for International Blood & Marrow Transplant Research, National Marrow Donor Program, Minneapolis, Minnesota;5. Department of Pathology, Stanford Medical School, Stanford University, Stanford, California;6. Germany National Bone Marrow Registry, Ulm, Germany;7. Blood and Marrow Transplant Program, Department of Medicine, University of Minnesota, Minneapolis, Minnesota
Abstract:Cytotoxic T-lymphocyte antigen-4 (CTLA-4) plays an essential role in T cell homeostasis by restraining immune responses. AG and GG genotypes of donor CTLA-4 SNP rs4553808 in patients after unrelated donor hematopoietic stem cell transplantations (HSCT) have been shown to be an independent predictor of inferior relapse-free survival (RFS) and overall survival (OS) compared with those with the AA genotype, in single-center studies. We tested the hypothesis that SNP rs4553808 is associated with RFS, OS, nonrelapse mortality (NRM) and the cumulative incidence of acute graft-versus-host disease (GVHD) and chronic GVHD in adults with acute myeloid leukemia and advanced myelodysplastic syndrome undergoing a first 8/8 or 7/8 HLA-matched unrelated donor HSCT. Multivariable analysis adjusting for relevant donor and recipient characteristics showed no significant association between SNP rs4553808 and OS, RFS, NRM, and incidence of acute and chronic GVHD. An exploratory analysis of other CTLA-4 SNPs, as well as studying the interaction with antithymocyte globulin, also demonstrated no significant associations. Our results indicate that CTLA-4 SNPs are not associated with HSCT outcomes.
Keywords:Cytotoxic T-lymphocyte antigen-4 (CTLA-4)  Single nucleotide polymorphisms (SNPs)  Hematopoietic stem cell transplantation
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