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DFFRY codes for a new human male-specific minor transplantation antigen involved in bone marrow graft rejection

Authors: M H, Vogt; R A, de Paus; P J, Voogt; R, Willemze; J H, Falkenburg;

DFFRY codes for a new human male-specific minor transplantation antigen involved in bone marrow graft rejection

Abstract

Graft rejection after histocompatibility locus antigen (HLA)-identical stem cell transplantation results from the recognition of minor histocompatibility antigens on donor stem cells by immunocompetent T lymphocytes of recipient origin. T-lymphocyte clones that specifically recognize H-Y epitopes on male target cells have been generated during graft rejection after sex-mismatched transplantation. Previously, 2 human H-Y epitopes derived from the same SMCY gene have been identified that were involved in bone marrow graft rejection. We report the identification of a new male-specific transplantation antigen encoded by the Y-chromosome-specific gene DFFRY. The DFFRY-derived peptide was recognized by an HLA-A1 restricted CTL clone, generated during graft rejection from a female patient with acute myeloid leukemia who rejected HLA-phenotypically identical bone marrow from her father. The identification of this gene demonstrates that at least 2 genes present on the human Y-chromosome code for male-specific transplantation antigens.

Related Organizations
Keywords

Graft Rejection, Male, H-Y Antigen, Molecular Sequence Data, Transfection, Peptide Fragments, Epitopes, Leukemia, Myeloid, Histocompatibility Antigens, Humans, Female, Amino Acid Sequence, HLA-A1 Antigen, Bone Marrow Transplantation, HeLa Cells, T-Lymphocytes, Cytotoxic

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Powered by OpenAIRE graph
citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
103
Top 10%
Top 10%
Top 10%