{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,26]],"date-time":"2026-08-26T15:03:28Z","timestamp":1787756608543,"version":"build-2784847793"},"reference-count":33,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2017,11,24]],"date-time":"2017-11-24T00:00:00Z","timestamp":1511481600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"DOI":"10.13039\/501100008895","name":"Tertiary Education Trust Fund","doi-asserted-by":"publisher","id":[{"id":"10.13039\/501100008895","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Tropical Med Int Health"],"published-print":{"date-parts":[[2018,1]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:title>Objective<\/jats:title><jats:p>Interleukin\u201010 (<jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201010) is an anti\u2010inflammatory cytokine produced by Th1 cells and macrophages. The rationale of this study was to examine and validate possible contributions of <jats:italic><jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201010<\/jats:italic> promoter polymorphisms in sub\u2010Saharan Africa in children infected with either <jats:italic>Plasmodium falciparum<\/jats:italic> or <jats:italic>Schistosoma haematobium<\/jats:italic> and in children co\u2010infected with both parasites.<\/jats:p><\/jats:sec><jats:sec><jats:title>Materials and Methods<\/jats:title><jats:p>A total of 309 Nigerian children aged 4\u201315 years were recruited. The study group consisted of individuals infected either with <jats:italic>P. falciparum<\/jats:italic> (<jats:italic>n<\/jats:italic> = 76) or <jats:italic>S. haematobium<\/jats:italic> (<jats:italic>n<\/jats:italic> = 94) in mono\u2010infections, a group of children co\u2010infected with both <jats:italic>P. falciparum<\/jats:italic> and <jats:italic>S. haematobium<\/jats:italic> (<jats:italic>n<\/jats:italic> = 62) and matched healthy controls (<jats:italic>n<\/jats:italic> = 77). The <jats:italic><jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201010<\/jats:italic> promoter polymorphisms \u20101082G\/A, \u2010819C\/T and \u2010592C\/A were genotyped by direct sequencing.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>The frequencies of the <jats:italic><jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201010 \u20101082<jats:styled-content style=\"fixed-case\">GG<\/jats:styled-content><\/jats:italic> genotype, the <jats:italic>\u20101082G<\/jats:italic> allele and haplotype <jats:italic><jats:styled-content style=\"fixed-case\">GCC<\/jats:styled-content><\/jats:italic> (positions \u20101082, \u2010819 and \u2010592) were higher in children infected with <jats:italic>P. falciparum<\/jats:italic> than in healthy controls, indicating that the <jats:italic>\u20101082<jats:styled-content style=\"fixed-case\">GG<\/jats:styled-content><\/jats:italic> genotype and the <jats:italic>\u20101082G<\/jats:italic> allele and the <jats:italic><jats:styled-content style=\"fixed-case\">GCC<\/jats:styled-content><\/jats:italic> haplotype are associated with increased susceptibility to malaria infection (<jats:styled-content style=\"fixed-case\">OR<\/jats:styled-content> = 3.4, 95% <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content> = 1.2\u201310.8, <jats:italic>P<\/jats:italic> = 0.02; <jats:styled-content style=\"fixed-case\">OR<\/jats:styled-content> = 2.5, 95% <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content> = 1.1\u20133.4, <jats:italic>P<\/jats:italic> = 0.02; <jats:styled-content style=\"fixed-case\">OR<\/jats:styled-content> = 3.8, 95% <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content> = 2.0\u20137.2, <jats:italic>P<\/jats:italic> = 0.0001, respectively). Children with the \u2010<jats:italic>1082<jats:styled-content style=\"fixed-case\">GG<\/jats:styled-content><\/jats:italic> genotype had a higher parasitaemia than children with the <jats:italic>\u20101082<jats:styled-content style=\"fixed-case\">AA<\/jats:styled-content><\/jats:italic> or <jats:italic>\u20101082<jats:styled-content style=\"fixed-case\">AG<\/jats:styled-content><\/jats:italic> genotypes (<jats:italic>P<\/jats:italic> = 0.0017). Haplotype <jats:italic><jats:styled-content style=\"fixed-case\">GCC<\/jats:styled-content><\/jats:italic> occurred more frequently in children infected with <jats:italic>S. haematobium,<\/jats:italic> while haplotype <jats:italic><jats:styled-content style=\"fixed-case\">GTA<\/jats:styled-content><\/jats:italic> was less frequent than in controls (<jats:styled-content style=\"fixed-case\">OR<\/jats:styled-content> = 2.2, 95% <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content> = 1.2\u20134.4, <jats:italic>P<\/jats:italic> = 0.017 and <jats:styled-content style=\"fixed-case\">OR<\/jats:styled-content> = 0.1, 95% <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content> = 0.02\u20130.5, <jats:italic>P<\/jats:italic> = 0.0004, respectively). No differences in the frequencies of <jats:italic><jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201010<\/jats:italic> promoter polymorphisms were observed between children with <jats:italic>P. falciparum<\/jats:italic>\u2013<jats:italic>S. haematobium<\/jats:italic> co\u2010infections and healthy controls.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>Although <jats:italic><jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201010<\/jats:italic> promoter polymorphisms are not associated with <jats:italic>P. falciparum<\/jats:italic> and <jats:italic>S. haematobium<\/jats:italic> co\u2010infection, variant \u20101082G\/A and haplotype <jats:italic><jats:styled-content style=\"fixed-case\">GCC<\/jats:styled-content><\/jats:italic> are associated with malaria, whereas the <jats:italic><jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201010<\/jats:italic> haplotypes <jats:italic><jats:styled-content style=\"fixed-case\">GCC<\/jats:styled-content><\/jats:italic> and <jats:italic><jats:styled-content style=\"fixed-case\">GTA<\/jats:styled-content><\/jats:italic> are associated with schistosomiasis.<\/jats:p><\/jats:sec>","DOI":"10.1111\/tmi.13007","type":"journal-article","created":{"date-parts":[[2017,11,13]],"date-time":"2017-11-13T12:56:41Z","timestamp":1510577801000},"page":"45-52","source":"Crossref","is-referenced-by-count":12,"title":["Differential contribution of interleukin\u201010 promoter variants in malaria and schistosomiasis mono\u2010 and co\u2010infections among Nigerian children"],"prefix":"10.1111","volume":"23","author":[{"given":"Ayodele","family":"Adedoja","sequence":"first","affiliation":[{"name":"Institute of Tropical Medicine University of T\u00fcbingen T\u00fcbingen Germany"},{"name":"Department of Medical Microbiology and Parasitology Ladoke Akintola University of Technology Osogbo Nigeria"},{"name":"Department of Medical Microbiology and Parasitology 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