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However, little information is available on the reaction of mononuclear phagocytes (<jats:styled-content style=\"fixed-case\">MNP<\/jats:styled-content>) to intestinal trematode infection, a reaction equally important in helminth\u2010based therapies. The <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>11c<jats:sup>+<\/jats:sup>\u00a0<jats:styled-content style=\"fixed-case\">CX<\/jats:styled-content>3<jats:styled-content style=\"fixed-case\">CR<\/jats:styled-content>1<jats:sup>+<\/jats:sup>\u00a0F4\/80<jats:sup>\u2212<\/jats:sup> <jats:styled-content style=\"fixed-case\">DC<\/jats:styled-content>s in the ileal lamina propria (<jats:styled-content style=\"fixed-case\">LP<\/jats:styled-content>) of the mouse were proven to migrate to the mesenteric lymph nodes (<jats:styled-content style=\"fixed-case\">MLN<\/jats:styled-content>s). We analyzed all <jats:styled-content style=\"fixed-case\">MNP<\/jats:styled-content> subsets present in the mouse <jats:styled-content style=\"fixed-case\">LP<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">MLN<\/jats:styled-content>s, under steady\u2010state conditions and during acute <jats:italic>Schistosoma mansoni<\/jats:italic>\u2010induced inflammation. Furthermore, we studied the uptake of schistosomal antigens by <jats:styled-content style=\"fixed-case\">MNP <\/jats:styled-content><jats:italic>in\u00a0vivo<\/jats:italic> in the <jats:styled-content style=\"fixed-case\">LP<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">MLN<\/jats:styled-content>s.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>Using a combination of immunohistochemistry and multiparametric flow cytometry, we investigated distributional changes of the <jats:styled-content style=\"fixed-case\">MNP<\/jats:styled-content> during acute intestinal schistosomiasis. Next, <jats:italic>S.\u00a0mansoni<\/jats:italic>\u2010derived products, i.e., <jats:italic>S.\u00a0mansoni<\/jats:italic> soluble worm proteins (Sm<jats:styled-content style=\"fixed-case\">SWP<\/jats:styled-content>) and <jats:italic>S.\u00a0mansoni<\/jats:italic> soluble egg antigens (Sm<jats:styled-content style=\"fixed-case\">SEA<\/jats:styled-content>) were intraperitoneally injected into <jats:styled-content style=\"fixed-case\">CX<\/jats:styled-content>3<jats:styled-content style=\"fixed-case\">CR<\/jats:styled-content>1<jats:sup>+\/<\/jats:sup><jats:styled-content style=\"fixed-case\"><jats:sup>GFP<\/jats:sup><\/jats:styled-content> C57BL\/6 mice and antigen uptake was analyzed using confocal microscopy.<\/jats:p><\/jats:sec><jats:sec><jats:title>Key Results<\/jats:title><jats:p>The <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>11c<jats:sup>+<\/jats:sup>\u00a0<jats:styled-content style=\"fixed-case\">CX<\/jats:styled-content>3<jats:styled-content style=\"fixed-case\">CR<\/jats:styled-content>1<jats:sup>+<\/jats:sup>\u00a0F4\/80<jats:sup>\u2212<\/jats:sup> <jats:styled-content style=\"fixed-case\">DC<\/jats:styled-content>s significantly increased during intestinal schistosomiasis in the <jats:styled-content style=\"fixed-case\">LP<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">MLN<\/jats:styled-content>s. Only <jats:styled-content style=\"fixed-case\">CX<\/jats:styled-content>3<jats:styled-content style=\"fixed-case\">CR<\/jats:styled-content>1\u2010expressing <jats:styled-content style=\"fixed-case\">DC<\/jats:styled-content> and M\u0424 subsets, but not other <jats:styled-content style=\"fixed-case\">LP DC<\/jats:styled-content>s, are involved in both Sm<jats:styled-content style=\"fixed-case\">SWP<\/jats:styled-content> and Sm<jats:styled-content style=\"fixed-case\">SEA<\/jats:styled-content> antigen uptake and processing.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions &amp; inferences<\/jats:title><jats:p>The significant upregulation of <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>11c<jats:sup>+<\/jats:sup>\u00a0<jats:styled-content style=\"fixed-case\">CX<\/jats:styled-content>3<jats:styled-content style=\"fixed-case\">CR<\/jats:styled-content>1<jats:sup>+<\/jats:sup>\u00a0F4\/80<jats:sup>\u2212<\/jats:sup> <jats:styled-content style=\"fixed-case\">DC<\/jats:styled-content>s during intestinal schistosomiasis and the restriction of phagocytosis of parasitic antigens to <jats:styled-content style=\"fixed-case\">CX<\/jats:styled-content>3<jats:styled-content style=\"fixed-case\">CR<\/jats:styled-content>1\u2010expresssing <jats:styled-content style=\"fixed-case\">MNP<\/jats:styled-content> indicate a crucial role for this immune cell niche in response to trematodiasis. These findings add insight into the functional specialization of <jats:styled-content style=\"fixed-case\">LP<\/jats:styled-content> immune cells and add to the understanding of cellular mechanisms behind helminth\u2010based therapies.<\/jats:p><\/jats:sec>","DOI":"10.1111\/nmo.12658","type":"journal-article","created":{"date-parts":[[2015,8,25]],"date-time":"2015-08-25T04:08:44Z","timestamp":1440475724000},"page":"1587-1599","source":"Crossref","is-referenced-by-count":2,"title":["Effect of schistosomiasis on <scp>CX<\/scp>3<scp>CR<\/scp>1\u2010expressing mononuclear phagocytes in the ileum and mesenteric lymph nodes of the mouse"],"prefix":"10.1111","volume":"27","author":[{"given":"K.","family":"Alpaerts","sequence":"first","affiliation":[{"name":"Laboratory of Cell Biology and Histology Department of Veterinary Sciences University of Antwerp Antwerp 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