HLA-Cw alleles associated with HLA extended haplotypes and C2 deficiency |
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| Authors: | O.P. Clavijo J.C. Delgado Z.L. Awdeh O. Fici D. Turbay C.A. Alper L. Truedsson E.J. Yunis |
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| Affiliation: | Department of Cancer Immunology and AIDS, Dana-Farber Cancer Institute, Boston, MA 02115, USA;Department of Pathology, Harvard Medical School Boston, MA 02115, USA;Department of Pathology, Brigham Women's Hospital, Boston, MA 02115, USA;The Center for Blood Research, Boston, MA 02115, USA;Department of Pediatrics, Harvard Medical School Boston, MA 02115, USA;Department of Medical Microbiology, Clinical Immunology Section, Lund University, Lund, Sweden |
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| Abstract: | Abstract: There are four MHC-linked complement genes, BF, C2, C4A and C4B, that are inherited as single DNA units, known as complotypes. Extended haplotypes were initially defined by studying the distribution of complotypes in relation to HLA-B and HLA-DR loci in Caucasian families. In order to analyze the distribution of HLA-Cw alleles in relation to extended haplotypes, we studied a large panel of MHC homozygous and heterozygous cell lines representing previously described Caucasian-derived extended haplotypes and 14 patients with complete C2 deficiency. HLA alleles were assigned using sequence-specific oligonucleotide probe hybridization (SSOP). Family analysis served to assign haplotypes for heterozygous samples. We found distinctive HLA-Cw alleles for each independent extended haplotype. Their association in each instance was statistically significant All patients with C2 deficiency carrying the haplotype [HLA-B18, S042, DR2] were associated with HLA-Cw*1203. These conserved allelic combinations may become an important tool for the study of human evolution and may contribute to the expeditious selection of prospective donors in clinical transplantation. |
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| Keywords: | C2 deficiency extended haplotypes HLA-Cw alleles MHC |
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