{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,4]],"date-time":"2026-04-04T12:04:23Z","timestamp":1775304263404,"version":"3.50.1"},"reference-count":54,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2013,7,11]],"date-time":"2013-07-11T00:00:00Z","timestamp":1373500800000},"content-version":"vor","delay-in-days":10,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Scand J Immunol"],"published-print":{"date-parts":[[2013,7]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Brucellosis remains a major zoonosis worldwide. Brucella antigens induce the production of T\u2010helper 1 (Th1) cytokines such as interleukin\u201012 (<jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201012) in humans. We aimed to investigate the association of two single nucleotide polymorphisms (<jats:styled-content style=\"fixed-case\">SNP<\/jats:styled-content>s) in the gene encoding the <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201012p40 cytokine (<jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201012B) with brucellosis and to examine the functionality of these <jats:styled-content style=\"fixed-case\">SNP<\/jats:styled-content>s through measuring serum levels of <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201012p40. We genotyped <jats:italic><jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201012B<\/jats:italic> gene rs3212227, A&gt;C; rs6887695\u00a0G&gt;C polymorphisms in a case\u2010control study on a total of 281 subjects including 153 patients with active brucellosis and 128 healthy controls, using <jats:styled-content style=\"fixed-case\">RFLP<\/jats:styled-content> and serum <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201012p40 levels, were assessed by <jats:styled-content style=\"fixed-case\">ELISA<\/jats:styled-content>. The rs3212227 minor allele (C) and homozygote genotype (<jats:styled-content style=\"fixed-case\">CC<\/jats:styled-content>) were more frequent in controls compared with patients with brucellosis (<jats:italic>P<\/jats:italic>\u00a0=\u00a00.006, <jats:styled-content style=\"fixed-case\">OR<\/jats:styled-content>\u00a0=\u00a00.608, 95%<jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\u00a0=\u00a00.429\u20130.861 for the C allele; <jats:italic>P<\/jats:italic>\u00a0=\u00a00.024, <jats:styled-content style=\"fixed-case\">OR<\/jats:styled-content>\u00a0=\u00a00.443, 95% <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>: 0.218\u20130.900 for the <jats:styled-content style=\"fixed-case\">CC<\/jats:styled-content> genotype). Comparison of <jats:italic><jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201012B<\/jats:italic> genotypes and serum levels of the <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201012p40 revealed that rs3212227 <jats:styled-content style=\"fixed-case\">AA<\/jats:styled-content> genotype, with higher frequency in patients than in controls, was associated with increased levels of the cytokine (<jats:italic>P<\/jats:italic>\u00a0=\u00a00.0001). Furthermore, the distribution of haplotype and genotype combinations in our study suggested that rs3212227C\/rs6887695C haplotype or <jats:styled-content style=\"fixed-case\">CC<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">GC<\/jats:styled-content> or <jats:styled-content style=\"fixed-case\">CC<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">CC<\/jats:styled-content> genotype combinations may protect controls against Brucella infection by contributing to a functional downregulation of the serum <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201012p40 production <jats:italic>in vivo<\/jats:italic>, as shown by <jats:styled-content style=\"fixed-case\">ELISA<\/jats:styled-content> (<jats:italic>P<\/jats:italic>\u00a0&lt;\u00a00.05). Overall, our study demonstrated that rs3212227 A variant was associated with higher levels of serum <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201012p40 and could possibly contribute to an inherited predisposition to brucellosis.<\/jats:p>","DOI":"10.1111\/sji.12054","type":"journal-article","created":{"date-parts":[[2013,4,12]],"date-time":"2013-04-12T05:12:42Z","timestamp":1365743562000},"page":"85-91","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":24,"title":["Levels of Interleukin\u2010(<scp>IL<\/scp>)\u201012p40 are Markedly Increased in Brucellosis Among Patients with Specific <i><scp>IL<\/scp>\u201012B<\/i> Genotypes"],"prefix":"10.1111","volume":"78","author":[{"given":"E.","family":"Eskandari\u2010Nasab","sequence":"first","affiliation":[{"name":"Infectious Diseases and Tropical Medicine Research Center Zahedan University of Medical Sciences Zahedan Iran"},{"name":"Department of Clinical Biochemistry School of Medicine Zahedan University of Medical Sciences Zahedan Iran"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M.","family":"Moghadampour","sequence":"additional","affiliation":[{"name":"Department of Microbiology School of Medicine Zahedan University of Medical Sciences Zahedan Iran"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A.","family":"Asadi\u2010Saghandi","sequence":"additional","affiliation":[{"name":"Department of Immunology School of Medicine Shahid Sadoughi University of Medical Sciences Yazd Iran"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"E.","family":"Kharazi\u2010nejad","sequence":"additional","affiliation":[{"name":"Department of Clinical Biochemistry School of Medicine Zahedan University of Medical Sciences Zahedan Iran"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A.","family":"Rezaeifar","sequence":"additional","affiliation":[{"name":"Department of Clinical Biochemistry 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