Immunogenetics of epitopes of the carboxyl terminus of the human 60-kD Ro autoantigen. 1995

R H Scofield, and W D Dickey, and K L Hardgrave, and B R Neas, and R M Horowitz, and R A McArthur, and A Fujisaku, and M B Frank, and J B Harley, and A ] Fujisak A [corrected to Fujisaku
Oklahoma Medical Research Foundation, Department of Medicine, University of Oklahoma Health Science Centre, Oklahoma City.

Systemic lupus erythematosus is associated with the presence of autoantibodies which bind several ribonucleoproteins, including Ro (or SS-A). We have explored the relationship of the HLA-DQ and T cell receptor alleles in patients producing autoantibodies binding the 13-kD carboxyl terminus fragment of the 60-kD Ro and with autoantibodies binding a peptide epitope within this fragment (amino acid residues 480-494). Antibodies binding the 13-kD fragment are more likely to be found in the sera of patients with particular DQA1 and DQB1 alleles, while antibodies binding the epitope at 480-494 are found almost exclusively in the sera of patients with a Bg/II 9.8-kb polymorphism of the T cell receptor beta gene. Meanwhile, in these same patient sera the level of autoantibodies binding the complete 60-kD Ro particle is associated with a distinct pattern of alleles at these same immunoregulatory loci. These data demonstrate that component parts of autoantibody responses may be under genetic control which can be distinguished from the HLA associations characteristic of the response to the intact, complete autoantigen.

UI MeSH Term Description Entries
D007074 Immunoglobulin G The major immunoglobulin isotype class in normal human serum. There are several isotype subclasses of IgG, for example, IgG1, IgG2A, and IgG2B. Gamma Globulin, 7S,IgG,IgG Antibody,Allerglobuline,IgG(T),IgG1,IgG2,IgG2A,IgG2B,IgG3,IgG4,Immunoglobulin GT,Polyglobin,7S Gamma Globulin,Antibody, IgG,GT, Immunoglobulin
D008180 Lupus Erythematosus, Systemic A chronic, relapsing, inflammatory, and often febrile multisystemic disorder of connective tissue, characterized principally by involvement of the skin, joints, kidneys, and serosal membranes. It is of unknown etiology, but is thought to represent a failure of the regulatory mechanisms of the autoimmune system. The disease is marked by a wide range of system dysfunctions, an elevated erythrocyte sedimentation rate, and the formation of LE cells in the blood or bone marrow. Libman-Sacks Disease,Lupus Erythematosus Disseminatus,Systemic Lupus Erythematosus,Disease, Libman-Sacks,Libman Sacks Disease
D008297 Male Males
D008969 Molecular Sequence Data Descriptions of specific amino acid, carbohydrate, or nucleotide sequences which have appeared in the published literature and/or are deposited in and maintained by databanks such as GENBANK, European Molecular Biology Laboratory (EMBL), National Biomedical Research Foundation (NBRF), or other sequence repositories. Sequence Data, Molecular,Molecular Sequencing Data,Data, Molecular Sequence,Data, Molecular Sequencing,Sequencing Data, Molecular
D011110 Polymorphism, Genetic The regular and simultaneous occurrence in a single interbreeding population of two or more discontinuous genotypes. The concept includes differences in genotypes ranging in size from a single nucleotide site (POLYMORPHISM, SINGLE NUCLEOTIDE) to large nucleotide sequences visible at a chromosomal level. Gene Polymorphism,Genetic Polymorphism,Polymorphism (Genetics),Genetic Polymorphisms,Gene Polymorphisms,Polymorphism, Gene,Polymorphisms (Genetics),Polymorphisms, Gene,Polymorphisms, Genetic
D004797 Enzyme-Linked Immunosorbent Assay An immunoassay utilizing an antibody labeled with an enzyme marker such as horseradish peroxidase. While either the enzyme or the antibody is bound to an immunosorbent substrate, they both retain their biologic activity; the change in enzyme activity as a result of the enzyme-antibody-antigen reaction is proportional to the concentration of the antigen and can be measured spectrophotometrically or with the naked eye. Many variations of the method have been developed. ELISA,Assay, Enzyme-Linked Immunosorbent,Assays, Enzyme-Linked Immunosorbent,Enzyme Linked Immunosorbent Assay,Enzyme-Linked Immunosorbent Assays,Immunosorbent Assay, Enzyme-Linked,Immunosorbent Assays, Enzyme-Linked
D005260 Female Females
D006683 HLA-DQ Antigens A group of the D-related HLA antigens found to differ from the DR antigens in genetic locus and therefore inheritance. These antigens are polymorphic glycoproteins comprising alpha and beta chains and are found on lymphoid and other cells, often associated with certain diseases. HLA-DC Antigens,HLA-MB Antigens,HLA-DC,HLA-DQ,HLA-DS,HLA-DS Antigens,HLA-LB,HLA-LB Antigens,HLA-MB,Antigens, HLA-DC,Antigens, HLA-DQ,Antigens, HLA-DS,Antigens, HLA-LB,Antigens, HLA-MB,HLA DC Antigens,HLA DQ Antigens,HLA DS Antigens,HLA LB Antigens,HLA MB Antigens
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000595 Amino Acid Sequence The order of amino acids as they occur in a polypeptide chain. This is referred to as the primary structure of proteins. It is of fundamental importance in determining PROTEIN CONFORMATION. Protein Structure, Primary,Amino Acid Sequences,Sequence, Amino Acid,Sequences, Amino Acid,Primary Protein Structure,Primary Protein Structures,Protein Structures, Primary,Structure, Primary Protein,Structures, Primary Protein

Related Publications

R H Scofield, and W D Dickey, and K L Hardgrave, and B R Neas, and R M Horowitz, and R A McArthur, and A Fujisaku, and M B Frank, and J B Harley, and A ] Fujisak A [corrected to Fujisaku
May 1997, Journal of clinical immunology,
R H Scofield, and W D Dickey, and K L Hardgrave, and B R Neas, and R M Horowitz, and R A McArthur, and A Fujisaku, and M B Frank, and J B Harley, and A ] Fujisak A [corrected to Fujisaku
March 1994, Clinical and experimental immunology,
R H Scofield, and W D Dickey, and K L Hardgrave, and B R Neas, and R M Horowitz, and R A McArthur, and A Fujisaku, and M B Frank, and J B Harley, and A ] Fujisak A [corrected to Fujisaku
April 1989, The Journal of clinical investigation,
R H Scofield, and W D Dickey, and K L Hardgrave, and B R Neas, and R M Horowitz, and R A McArthur, and A Fujisaku, and M B Frank, and J B Harley, and A ] Fujisak A [corrected to Fujisaku
January 1995, Journal of clinical laboratory analysis,
R H Scofield, and W D Dickey, and K L Hardgrave, and B R Neas, and R M Horowitz, and R A McArthur, and A Fujisaku, and M B Frank, and J B Harley, and A ] Fujisak A [corrected to Fujisaku
December 1994, Genes & development,
R H Scofield, and W D Dickey, and K L Hardgrave, and B R Neas, and R M Horowitz, and R A McArthur, and A Fujisaku, and M B Frank, and J B Harley, and A ] Fujisak A [corrected to Fujisaku
March 2010, PloS one,
R H Scofield, and W D Dickey, and K L Hardgrave, and B R Neas, and R M Horowitz, and R A McArthur, and A Fujisaku, and M B Frank, and J B Harley, and A ] Fujisak A [corrected to Fujisaku
January 1992, Autoimmunity,
R H Scofield, and W D Dickey, and K L Hardgrave, and B R Neas, and R M Horowitz, and R A McArthur, and A Fujisaku, and M B Frank, and J B Harley, and A ] Fujisak A [corrected to Fujisaku
September 1994, Arthritis and rheumatism,
R H Scofield, and W D Dickey, and K L Hardgrave, and B R Neas, and R M Horowitz, and R A McArthur, and A Fujisaku, and M B Frank, and J B Harley, and A ] Fujisak A [corrected to Fujisaku
October 1995, Lupus,
R H Scofield, and W D Dickey, and K L Hardgrave, and B R Neas, and R M Horowitz, and R A McArthur, and A Fujisaku, and M B Frank, and J B Harley, and A ] Fujisak A [corrected to Fujisaku
January 1991, The Journal of clinical investigation,
Copied contents to your clipboard!