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Medline ® Abstract for Reference 71

of 'Epidemiology of, risk factors for, and possible causes of rheumatoid arthritis'

71
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Genetic bias in immune responses to a cassette shared by different microorganisms in patients with rheumatoid arthritis.
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La Cava A, Nelson JL, Ollier WE, MacGregor A, Keystone EC, Thorne JC, Scavulli JF, Berry CC, Carson DA, Albani S
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J Clin Invest. 1997;100(3):658.
 
Rheumatoid arthritis (RA) is an autoimmune disease associated with HLA-DRbeta1 alleles which contain the QKRAA amino acid sequence in their third hypervariable region(s). The QKRAA sequence is also expressed by several human pathogens. We have shown previously that an Escherichia coli peptide encompassing QKRAA is a target of immune responses in RA patients. Here we address two questions: first, whether QKRAA may function as an "immunological cassette" with similar, RA-associated, immunogenic properties when expressed by other common human pathogens; and second, what is the influence of genetic background in the generation of these responses. We find that early RA patients have enhanced humoral and cellular immune responses to Epstein-Barr virus and Brucella ovis and Lactobacillus lactis antigens which contain the QKRAA sequence. These results suggest that the QKRAA sequence is an antigenic epitope on several different microbial proteins, and that RA patients recognize the immunological cassette on different backgrounds. ANOVA of immune responses to "shared epitope" antigens in monozygotic twin couples shows that, despite significantly elevated responses in affected individuals, a similarity between pairs is retained, thus suggesting a role played either by hereditary or shared environmentalfactors in the genesis or maintenance of these responses.
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Department of Medicine, University of California, San Diego, La Jolla, California 92093-0663, USA. antonio@ucsd.edu
PMID