{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,18]],"date-time":"2026-09-18T11:00:57Z","timestamp":1789729257458,"version":"4.0.1"},"reference-count":35,"publisher":"Wiley","issue":"10","license":[{"start":{"date-parts":[[2016,12,10]],"date-time":"2016-12-10T00:00:00Z","timestamp":1481328000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"name":"The Department of Science and Technology-Scientific and Engineering Research Board, New Delhi, India","award":["SR\/SO\/HS-0067\/2012"],"award-info":[{"award-number":["SR\/SO\/HS-0067\/2012"]}]}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Int J of Rheum Dis"],"published-print":{"date-parts":[[2017,10]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:title>Aim<\/jats:title><jats:p>To investigate the presence of the \u2018shared epitope\u2019 (<jats:styled-content style=\"fixed-case\">SE<\/jats:styled-content>) in the<jats:italic><jats:styled-content style=\"fixed-case\">HLA<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">DRB<\/jats:styled-content>1<\/jats:italic>alleles in patients with<jats:styled-content style=\"fixed-case\">RA<\/jats:styled-content>and to ascertain the frequency of the<jats:italic><jats:styled-content style=\"fixed-case\">HLA<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">DRB<\/jats:styled-content>1<\/jats:italic>alleles with autoantibodies (anti\u2010cyclic citrullinated peptide [anti\u2010<jats:styled-content style=\"fixed-case\">CCP<\/jats:styled-content>] rheumatoid factor [<jats:styled-content style=\"fixed-case\">RF<\/jats:styled-content>]) and disease severity.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>A total of 200<jats:styled-content style=\"fixed-case\">RA<\/jats:styled-content>patients and 200 apparently healthy subjects participated in the study.<jats:italic><jats:styled-content style=\"fixed-case\">HLA<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">DRB<\/jats:styled-content>1<\/jats:italic>were genotyped using polymerase chain reaction with sequence\u2010specific primer (<jats:styled-content style=\"fixed-case\">PCR<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">SSP<\/jats:styled-content>). Anti\u2010<jats:styled-content style=\"fixed-case\">CCP<\/jats:styled-content>and<jats:styled-content style=\"fixed-case\">RF<\/jats:styled-content>in serum were determined by<jats:italic>in vitro<\/jats:italic>quantitative enzyme\u2010linked immunosorbent assay (<jats:styled-content style=\"fixed-case\">ELISA<\/jats:styled-content>) method. Erythrocyte sedimentation rate (<jats:styled-content style=\"fixed-case\">ESR<\/jats:styled-content>) was measured by Westergren method. Disease activity was assessed by using the disease activity score\u201028 (<jats:styled-content style=\"fixed-case\">DAS<\/jats:styled-content>\u201028). Chi\u2010square test and Student's<jats:italic>t<\/jats:italic>\u2010test were used in the statistical analysis.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>A significant increase in the frequency of<jats:italic><jats:styled-content style=\"fixed-case\">HLA<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">DRB<\/jats:styled-content>1<\/jats:italic>*01, *04, *10 and *14 were identified in<jats:styled-content style=\"fixed-case\">RA<\/jats:styled-content>patients and showed a strong association with the disease susceptibility. While the frequencies of<jats:italic><jats:styled-content style=\"fixed-case\">HLA<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">DRB<\/jats:styled-content>1<\/jats:italic>*03, *07, *11 and *13 were significantly lower in<jats:styled-content style=\"fixed-case\">RA<\/jats:styled-content>patients than in controls. The other<jats:italic><jats:styled-content style=\"fixed-case\">HLA<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">DRB<\/jats:styled-content>1<\/jats:italic>alleles *08, *09, *12, *15 and *16 showed no significant difference. The frequency of anti\u2010<jats:styled-content style=\"fixed-case\">CCP<\/jats:styled-content>and<jats:styled-content style=\"fixed-case\">RF<\/jats:styled-content>antibodies did not showed significant difference in<jats:styled-content style=\"fixed-case\">SE<\/jats:styled-content>\u2010positive patients compared with<jats:styled-content style=\"fixed-case\">SE<\/jats:styled-content>\u2010negative patients.<jats:styled-content style=\"fixed-case\">DAS<\/jats:styled-content>\u201028 values of<jats:styled-content style=\"fixed-case\">RA<\/jats:styled-content>patients showed no significant difference between<jats:styled-content style=\"fixed-case\">SE<\/jats:styled-content>\u2010positive and<jats:styled-content style=\"fixed-case\">SE<\/jats:styled-content>\u2010negative groups.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>Our results indicate that<jats:italic><jats:styled-content style=\"fixed-case\">HLA<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">DRB<\/jats:styled-content>1<\/jats:italic>*01, *04, *10 and *14 alleles are related with<jats:styled-content style=\"fixed-case\">RA<\/jats:styled-content>, while<jats:italic><jats:styled-content style=\"fixed-case\">HLA<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">DRB<\/jats:styled-content>1<\/jats:italic>*03, *07, *11 and *13 protect against<jats:styled-content style=\"fixed-case\">RA<\/jats:styled-content>in our population. 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