1. Evidence for multiple shared antigenic determinants within Ro60 and other lupus-related ribonucleoprotein autoantigens in human autoimmune responses.
- Author
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Pal R, Deshmukh US, Ohyama Y, Fang Q, Kannapell CC, Gaskin F, and Fu SM
- Subjects
- Amino Acid Sequence, Antibodies, Monoclonal immunology, Cross Reactions, Enzyme-Linked Immunosorbent Assay, Humans, Molecular Sequence Data, Polymerase Chain Reaction, Ribonucleoproteins, Small Nuclear immunology, Sequence Homology, Amino Acid, snRNP Core Proteins, Autoantibodies immunology, Autoantigens immunology, Autoimmunity immunology, Epitopes, B-Lymphocyte immunology, Lupus Erythematosus, Systemic immunology, RNA, Small Cytoplasmic immunology, Ribonucleoproteins immunology
- Abstract
Ab responses directed against several ribonucleoprotein (RNP) Ags are a characteristic feature of systemic lupus erythematosus (SLE). Previous work in our laboratory using mouse model systems had revealed that both epitope spreading and inherent cross-reactivity between ribonucleoproteins contributes to the observed multiple specificities in autoimmune sera. We have now extended these studies to human autoimmune responses. Using purified polyclonal and mAbs derived from SLE patients, cross-reactivity between Ro60 and SmD was demonstrated. The cross-reactive epitope was mapped to nonhomologous regions on Ro60(481-505) and SmD(88-102). Five mAbs specifically recognized apoptotic cells, demonstrated variable levels of cross-reactivity toward other nonhomologous ribonucleoprotein targets and bound multiple, nonoverlapping and nonhomologous epitopes on Ro60. Our study demonstrates that cross-reactivity between frequently targeted autoantigens is an important aspect of human systemic autoimmune responses. The presence of multiple cross-reactive epitopes on Ro60 might be important for the generation of anti-Ro60 Ab in SLE patients and in normal individuals displaying no evidence of clinical disease.
- Published
- 2005
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