Minor histocompatibility antigens (minor H antigens) are targets of graft-versus-host disease and graft-versus-leukemia responses after allogeneic human leukocyte antigen identical hematopoietic stem cell transplantation. Only a few human minor H antigens have been molecularly characterized and in all cases, amino acid differences between homologous donor and recipient proteins due to nucleotide polymorphisms in the respective genes were responsible for immunogenicity. Here, we have used cDNA expression cloning to identify a novel human minor H antigen encoded by UGT2B17, an autosomal gene in the multigene UDP-glycosyltransferase 2 family that is selectively expressed in liver, intestine, and antigen-presenting cells. In contrast to previously defined human minor H antigens, UGT2B17 is immunogenic because of differential expression of the protein in donor and recipient cells as a consequence of a homozygous gene deletion in the donor. Deletion of individual members of large gene families is a common form of genetic variation in the population and our results provide the first evidence that differential protein expression as a consequence of gene deletion is a mechanism for generating minor H antigens in humans.
A Human Minor Histocompatibility Antigen Resulting from Differential Expression due to a Gene Deletion
M. Murata is on leave from Nagoya University Graduate School of Medicine, Nagoya 466 8550, Japan.
Abbreviations used in this paper: B-LCL, Epstein Barr virus transformed lymphoblastoid cells; CYP, cytochrome P450; DC, dendritic cells; GST, glutathione S-transferase; HSCT, hematopoietic stem cell transplantation; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; GVL, graft-versus-leukemia; minor H antigens, minor histocompatibility antigens; SSP-PCR, sequence specific primer-PCR; UGT2B17, UDP glycosyltransferase 2 family, polypeptide B17.
Makoto Murata, Edus H. Warren, Stanley R. Riddell; A Human Minor Histocompatibility Antigen Resulting from Differential Expression due to a Gene Deletion . J Exp Med 19 May 2003; 197 (10): 1279–1289. doi: https://doi.org/10.1084/jem.20030044
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