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Differential behavior of cytotoxic effector cells against HLA antigens in strong genetic linkage disequilibrium
Authors:Se Jong Kim  Frank T Christiansen  Donald M Silver  Bo Dupont
Institution:(1) Human Immunogenetic Section, Sloan-Kettering Institute for Cancer Research, 1250 First Avenue, 10021 New York, New York;(2) Sloan-Kettering Institute for Cancer Research, 1250 First Avenue, Box 41, 10021 New York, New York;(3) Present address: Department of Microbiology, Yonsei University, College of Medicine, Seoul, Korea;(4) Present address: Department of Clinical Immunology, Royal Perth Hospital, 6000 Perth, Western Australia
Abstract:Five sets of cytotoxic effector cells were generated, using haploidentical, first degree relatives in five different families, against the HLA-A3; B7 serological determinants combined with different DR antigens. When tested against a panel of cells bearing combinations of the HLA-A, -B and -DR antigens it was shown that the HLA-B7 antigen was as strong a CML target determinant alone as it was in the presence of HLA-A3. The strength of the HLA-A3 antigen as target determinant varied. With effector cells primed to the HLA-A3; B7; DR2 haplotype, the A3 antigen alone behaved as a weak target determinant. When the same target cells were tested with the effector cells generated against HLA-A3; B7 without DR2, the A3 antigen behaved as a strong target determinant. A number of target cells lacking the serologically detectable HLA determinants present on the sensitizing HLA haplotype were identified as being killed by specific effector cells. These data suggest either a number of new CML target determinants controlled by different loci or the presence of a single, new locus with multiple alleles controlling CML targets.
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