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Cim: an MHC class II-linked allelism affecting the antigenicity of a classical class I molecule for T lymphocytes
Authors:Alexandra M Livingstone  Simon J Powis  Eberhard Günther  Donald V Cramer  Jonathan C Howard  Geoffrey W Butcher
Institution:(1) Department of Immunology, AFRC Institute of Animal Physiology and Genetics Research, Cambridge Research Station, CB2 4AT Cambridge, Babraham, UK;(2) Max Planck Institut für Immunbiologie, W-7800 Freiburg, Federal Republic of Germany;(3) Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA;(4) Present address: Basel Institute for Immunology, 487 Grenzacherstrasse, CH-4005 Basel, Switzerland;(5) Present address: Abteilung Immungenetik der Universität, Gosslerstrasse 12d, W-3400 Göttingen, Federal Republic of Germany;(6) Present address: Department of Surgery, 607 Schuman Hall, Cedar Sinai Medical Centre, 8700 Beverley Boulevard, 90048 Los Angeles, CA, USA
Abstract:Two alleles at the major histocompatibility complex (MHC)-linked locus cim determine ldquogain and lossrdquo changes in the rat RT1.Aa class I molecule which affect its structure both as an alloantigen and as a restriction element. Alleles at the cim locus also influence the post-translational modification of RT1.Aa. These effects may reflect the participation of the cim gene product in the processes of peptide loading or assembly of RT1.Aa. In this study we have used the discriminating RT1.Aa-specific monoclonal antibody JY3/84, as well as cytotoxic T cells raised in appropriate combinations, to determine the cim alleles of eight haplotypes in 15 independent inbred strains of rat. We have also employed the same techniques to analyse a panel of F1 hybrid animals derived from various MHC recombinant strains. These experiments map the cim locus to the class II region of RT1, probably between the DP-related genes (RT1.H) and the DQ-related RT1.Bagr. Address correspondence and offprint requests to: G. W. Butcher.
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