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Novel HLA-B alleles, B*8201, B*3515 and B*5106, add to the complexity of serologic identification of HLA types
Authors:C. K. Hurley  N. Steiner  R. J. Hoyer  E. Menchaca  W. Mitton  T. Simonis  R. J. Hartzman  A. H. Johnson  J. Ng
Affiliation:Department of Microbiology and Immunology, Georgetown University Medical School, Washington, DC;Transplant Immunology, Wilford Hall Medical Center, Lackland Air Force Base, Texas;Naval Medical Research Institute, Bethesda, Maryland;HLA Laboratory, National Institutes of Health, Bethesda, Maryland;Department of Pediatrics, Georgetown University Medical School, Washington, DC, USA
Abstract:
Three class I alleles, B*8201, B*3515 and B*5106, have been described using DNA and cDNA sequencing. The B*8201 allele is most structurally related to B*5602, differing from it by 14 nucleotide substitutions resulting in 5 amino acid differences. The other two alleles, B*3515 and B*5106, differ from their most closely related HLA-B alleles by 2–3 nucleotide substitutions resulting in 1–2 amino acid substitutions, respectively. The majority of nucleotide substitutions marking these new alleles are observed in other HLA-B alleles suggesting that gene conversion and/or reciprocal recombination have created this diversity. All of the amino acid substitutions are predicted to alter the antigen binding site of the HLA-B molecule. The newly defined HLA-B allelic products were originally defined by their unusual serologic reactivity patterns. The B*8201 allelic product is serologically typed as a B "blank" or as a variant of B22 or B45. These patterns and the serologic reactivity of the other newly described allelic products are consistent with the protein sequence homology among specific HLA-B molecules. While serology remains a powerful tool for detecting HLA diversity, alleles generated by events resulting in the sharing of HLA sequence polymorphisms among alleles at a locus will continue to create complexity in the interpretation of typing results.
Keywords:HLA-B    B*8201    B*3515    B*5106
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