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Polymorphism of the HLA DR1 haplotype in the Israeli population investigated at the serological,cellular, and genomic levels
Authors:Nadine Cohen  Adam Friedmann  Fanny Szafer  Avraham Amar  Daniel Cohen  Prof Chaim Brautbar
Institution:(1) The Lautenberg Center for General and Tumor Immunology, The Hebrew University, Hadassah Medical School, Jerusalem, Israel;(2) Department of Genetics, Life Science, Hebrew University, Jerusalem, Israel;(3) Tissue Typing Unit, Department of Clinical Microbiology, Hadassah University Hospital, Kiryat Hadassah, Jerusalem, Israel;(4) Inserm U93, Hôpital Saint-Louis, Paris, France
Abstract:In the present report, we used serological, cellular, and restriction fragment length polymorphism (RFLP) to investigate the DR1 haplotype in the Israeli population. We describe an Israeli homozygous typing cell (HTC), HLA-DwldquoLVArdquo, which defines a new lymphocyte-activating determinant associated with Bw65, DR1 and distinct from Dwl. The parents of this donor, non-Ashkenazi Algerian Jews, are first cousins and share HLA-Cw8, Bw65, BfS, DR1, DQw1, DPw4. No specificity could be assigned to HLA-DwldquoLVArdquo using the 91 Ninth Workshop HTCs. Two families and forty unrelated DR1 individuals were studied with DwldquoLVArdquo and a panel of DR1/Dw1 HTCs. HLA-DwldquoLVArdquo showed segregation as a single determinant within families. This new specificity was present in 24 out of 40 (60%) unrelated DR1 individuals, indicating that in the Israeli population DwldquoLVArdquo is the main lymphocyte-defined determinant associated with the serologically defined DRI specificity, in contrast to non-Jewish Caucasoids where DR1 is significantly associated with Dw1. The vast majority of DwldquoLVArdquo-positive carriers were also Bw65 carriers, indicating that Bw65, DR1, DwldquoLVArdquo may represent a typical allele combination in the Israeli population. The RFLP analysis established the correlation of certain RFLPs with Dw1 and DwldquoLVArdquo. In addition, we describe a cluster of RFLPs that may correspond to a new Dw subtype associated with DR1, for which no serological and cellular reagents have been described so far.
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