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Further DNA sequence microheterogeneity of the HLA-DR4/Dw13 haplotype group: Importance of amino acid position 86 of the DRβ1 chain for T-cell recognition
Authors:Bernhard Lang   Cristina Navarrete   Peter R. LoGalbo   Gerald T. Nepom   Jack Silver   Robert J. Winchester  Peter K. Gregersen
Affiliation:

a Cellular and Molecular Biology Unit, Department of Rheumatic Diseases, Hospital for Joint Diseases, New York University School of Medicine, New York, New York, USA

b Department of Immunology, Virginia Mason Research Center, Seattle, Washington, USA

Abstract:Using the polymerase chain reaction we have isolated and sequenced cDNA clones corresponding to the polymorphic first domain of the DRβ1 chain from the DR4, “Dw13” cell line, JHa. We have found that the JHa DRβ1 allele differs from previously reported Dw13 alleles by a single amino acid substitution at position 86. The functional relevance of this polymorphism is supported by the reactivity pattern of a T-cell clone, E38. E38 is an alloreactive T-cell clone which reacts with all Dw14 stimulator cells and all Dw13-positive cells tested except the “Dw13”- positive homozygous typing cell line JHa. Inhibition studies with monoclonal antibodies revealed the stimulating determinant to be on DR and not on DQ or DP molecules. These data indicate that position 86 of the DRβ1 chain can play an important role in the formation of determinants recognized by T cells.
Keywords:HTC, homozygous typing cell line   MoAb, monoclonal antibody   LCL, Epstein-Bar virus-transformed   PBL, peripheral blood mononuclear   MHC, lymphoblastoid cell line major histocompatibility   PCR, cell   MLR, complex mixed lymphocyte reaction   PLT, polymerase chain reaction primed lymphocyte typing
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