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Blood ; 99(8): 3027-32, 2002 Apr 15.
Article in English | MEDLINE | ID: mdl-11929796

ABSTRACT

Graft rejection or graft-versus-host (GVH) disease after HLA-identical stem cell transplantation is the result of recognition of minor histocompatibility antigens (mHags) by immunocompetent T lymphocytes from recipient or donor origin, respectively. Cytolytic T lymphocyte (CTL) clones can be isolated during graft rejection and GVH disease to identify mHags and their corresponding genes. Thus far, all human mHags identified appeared to be HLA class I-restricted. Here, we report the characterization of the first human HLA class II-restricted sex-linked mHag involved in GVH disease. Previously, we isolated an HLA-DQ5-restricted CD4(+) CTL clone from a male patient with chronic myeloid leukemia who developed acute GVH disease grade III-IV after transplantation of HLA genotypically identical female stem cells. Using a panel of female HLA-DQ5(+) EBV cells that we stably transfected with Y chromosome-specific genes, we determined that the HLA class II male-specific mHag (H-Y) was encoded by the Y chromosome-specific gene DBY. The H-Y epitope was localized in the DBY protein using female HLA-DQ5(+) peripheral blood mononuclear cells loaded with DBY protein fragments. The minimal peptide sequence leading to maximal recognition by the specific HLA-DQ5-restricted CTL clone was characterized as the 12-amino acid sequence HIENFSDIDMGE. Although the epitope differed by 3 amino acids from its X-homolog DBX, only 2 polymorphisms were shown to be essential for recognition by the CTL clone.


Subject(s)
Graft vs Host Disease/immunology , HLA-DQ Antigens/immunology , Minor Histocompatibility Antigens/immunology , Proteins/immunology , Y Chromosome , Amino Acid Sequence , CD4-Positive T-Lymphocytes/immunology , DEAD-box RNA Helicases , Epitope Mapping , Epitopes/analysis , Epitopes/genetics , Epitopes/immunology , Female , Genetic Linkage , Hematopoietic Stem Cell Transplantation/adverse effects , Histocompatibility Antigens Class II/genetics , Histocompatibility Antigens Class II/immunology , Humans , Male , Minor Histocompatibility Antigens/genetics , Oligopeptides/chemical synthesis , Oligopeptides/immunology , Proteins/genetics , T-Lymphocytes, Cytotoxic/immunology
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