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Eur J Haematol ; 89(6): 497-500, 2012 Dec.
Article in English | MEDLINE | ID: mdl-23033942

ABSTRACT

Mismatched human leukocyte antigens (HLAs) on leukemic cells can be targeted by donor T cells in HLA-mismatched/haploidentical stem cell transplantation. In two cases of acute myeloid leukemia with t(6;11)(q27;q23) abnormality presented here, flow cytometry analysis showed a lack of HLA-A unshared between recipients and donors in relapsing leukemic cells after HLA-haploidentical transplantation. However, high-resolution HLA genotyping showed that one case lacked a corresponding HLA haplotype, whereas the other preserved it. These cases suggest that leukemic cells, which lacked mismatched HLA expression, might have an advantage in selective expansion under donor T-cell immune surveillance after HLA-haploidentical transplantation. Most importantly, down-regulation of unshared HLA expression potentially occurs by genetic alterations other than loss of HLA alleles.


Subject(s)
Bone Marrow Transplantation , HLA Antigens/genetics , Hematopoietic Stem Cell Transplantation , Leukemia, Myeloid, Acute/genetics , Adult , Chromosomes, Human, Pair 11/immunology , Chromosomes, Human, Pair 6/immunology , Female , Graft vs Host Disease/genetics , HLA Antigens/immunology , Haplotypes , Histocompatibility , Histocompatibility Testing , Humans , Leukemia, Myeloid, Acute/immunology , Recurrence , T-Lymphocytes/immunology , Tissue Donors , Translocation, Genetic/immunology , Transplantation, Homologous
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