{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,11]],"date-time":"2026-07-11T18:00:37Z","timestamp":1783792837032,"version":"3.55.0"},"reference-count":48,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2015,1,28]],"date-time":"2015-01-28T00:00:00Z","timestamp":1422403200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"name":"Instituto Maimonides para investigacion Biomedica de Cordoba (IMIBIC)"},{"name":"Rheumatology Department, Reina Sophia Hospital, Cordoba"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Tissue Antigens"],"published-print":{"date-parts":[[2015,2]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Ankylosing spondylitis (<jats:styled-content style=\"fixed-case\">AS<\/jats:styled-content>) is very often associated with human leukocyte antigen (<jats:styled-content style=\"fixed-case\">HLA<\/jats:styled-content>), particularly <jats:italic><jats:styled-content style=\"fixed-case\">HLA<\/jats:styled-content>\u2010B*27<\/jats:italic>. However, the strength of this association and clinical features may vary in different ethnic groups. Our study aims to assess the distribution of <jats:styled-content style=\"fixed-case\">HLA<\/jats:styled-content>\u2010A, \u2010B, \u2010Cw and <jats:styled-content style=\"fixed-case\">DRB1<\/jats:styled-content> alleles in Moroccan patients with <jats:styled-content style=\"fixed-case\">AS<\/jats:styled-content> and to compare the clinical features of <jats:styled-content style=\"fixed-case\">AS<\/jats:styled-content> and the frequencies of <jats:styled-content style=\"fixed-case\">HLA\u2010B27<\/jats:styled-content> in patients from Morocco with other series. Seventy\u2010five patients diagnosed with <jats:styled-content style=\"fixed-case\">AS<\/jats:styled-content> and assessed for clinical manifestations were selected and compared to 100 healthy controls. <jats:styled-content style=\"fixed-case\">HLA<\/jats:styled-content> class I and <jats:styled-content style=\"fixed-case\">II<\/jats:styled-content> antigens were typed by polymerase chain reaction sequence\u2010specific oligonucleotide. <jats:styled-content style=\"fixed-case\">HLA\u2010B27<\/jats:styled-content> subtypes were studied by polymerase chain reaction amplification with sequence\u2010specific primers. <jats:styled-content style=\"fixed-case\">HLA<\/jats:styled-content>\u2010B27 was found in 64% of patients. It was positively associated with younger age at disease onset, family history, and uveitis while it had a negative association with late onset. Six <jats:italic>B*27<\/jats:italic> subtypes were identified in the <jats:styled-content style=\"fixed-case\">AS<\/jats:styled-content> group. <jats:italic><jats:styled-content style=\"fixed-case\">HLA<\/jats:styled-content>\u2010B*2705<\/jats:italic> and <jats:italic>B*2702<\/jats:italic> were the most common observed subtypes. Among other <jats:styled-content style=\"fixed-case\">HLA<\/jats:styled-content> genes, a significant increase in the prevalence of <jats:italic><jats:styled-content style=\"fixed-case\">HLA<\/jats:styled-content>\u2010Cw*02<\/jats:italic> and <jats:italic><jats:styled-content style=\"fixed-case\">HLA\u2010DRB<\/jats:styled-content>*15<\/jats:italic> was found in <jats:styled-content style=\"fixed-case\">AS<\/jats:styled-content> patients. <jats:styled-content style=\"fixed-case\">HLA\u2010B27<\/jats:styled-content> is involved in the predisposition of <jats:styled-content style=\"fixed-case\">AS<\/jats:styled-content> in the Moroccan population. <jats:italic><jats:styled-content style=\"fixed-case\">HLA<\/jats:styled-content>\u2010B*2705<\/jats:italic> and <jats:italic>B*2702<\/jats:italic> were the predominant subtypes supporting previous reports in Caucasian spondyloarthropathies. Other <jats:styled-content style=\"fixed-case\">HLA<\/jats:styled-content> genes, <jats:italic><jats:styled-content style=\"fixed-case\">HLA<\/jats:styled-content>\u2010Cw*02<\/jats:italic> and <jats:italic><jats:styled-content style=\"fixed-case\">HLA\u2010DRB1<\/jats:styled-content>*15<\/jats:italic>, seem to confer predisposing effect to the disease. However, the lower frequency of <jats:styled-content style=\"fixed-case\">HLA<\/jats:styled-content>\u2010<jats:italic><jats:styled-content style=\"fixed-case\">B27<\/jats:styled-content><\/jats:italic> compared to the literature in our study suggests the existence of different genetic and\/or environmental factors in Morocco.<\/jats:p>","DOI":"10.1111\/tan.12515","type":"journal-article","created":{"date-parts":[[2015,1,28]],"date-time":"2015-01-28T07:59:03Z","timestamp":1422431943000},"page":"108-116","source":"Crossref","is-referenced-by-count":14,"title":["Polymorphisms of HLA\u2010A, \u2010B, \u2010Cw and DRB1 antigens in Moroccan patients with ankylosing spondylitis and a comparison of clinical features with frequencies of <i>HLA\u2010B*27<\/i>"],"prefix":"10.1111","volume":"85","author":[{"given":"I.","family":"El Mouraghi","sequence":"first","affiliation":[{"name":"Department of Biology, Faculty of Sciences University Abdelmalek Essaidi  T\u00e9touan 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