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• W2014820797 abstract "Many immune-mediated diseases are associated with particular MHC class I or class II alleles. In rheumatoid arthritis (RA-shared), the vast majority of patients possess HLA-DRB1 alleles encoding a shared epitope, which is a five-amino acid sequence motif in positions 70-74 of the HLA-DRbeta chain. The mechanistic basis for this association is unknown. Here we discuss recent evidence suggesting that the shared epitope may act as an allele-specific ligand that triggers increased nitric oxide (NO) production in opposite cells with resultant immune dysregulation. We propose that by doing that, the RA-shared shared epitope may form an unintended bridge between the innate and adaptive immune systems, thereby allowing aberrant signaling events that could trigger disease." @default.
• W2014820797 created "2016-06-24" @default.
• W2014820797 creator A5021304310 @default.
• W2014820797 creator A5053328220 @default.
• W2014820797 date "2007-09-01" @default.
• W2014820797 modified "2023-09-23" @default.
• W2014820797 title "Nitric Oxide Signaling Triggered by the Rheumatoid Arthritis Shared Epitope: A New Paradigm for MHC Disease Association?" @default.
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• W2014820797 doi "https://doi.org/10.1196/annals.1423.009" @default.
• W2014820797 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/17911422" @default.
• W2014820797 hasPublicationYear "2007" @default.
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