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When <jats:styled-content style=\"fixed-case\">TLR<\/jats:styled-content>\u2010stimulated eosinophils were inoculated i.p. into wild\u2010type mice, and <jats:styled-content style=\"fixed-case\">NK<\/jats:styled-content> cells were rapidly recruited and exhibited antitumour cytotoxicity. However, when mice depleted of <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>11c<jats:sup>+<\/jats:sup> cells were used, a marked decrease in the number of recruited <jats:styled-content style=\"fixed-case\">NK<\/jats:styled-content> cells was observed. We postulated that CpG or <jats:styled-content style=\"fixed-case\">LPS<\/jats:styled-content> from the injected eosinophils could be transferred to host cells, which in turn could recruit <jats:styled-content style=\"fixed-case\">NK<\/jats:styled-content> cells. However, by inoculating mice deficient in <jats:styled-content style=\"fixed-case\">TLR<\/jats:styled-content>4 or <jats:styled-content style=\"fixed-case\">TLR<\/jats:styled-content>9 with <jats:styled-content style=\"fixed-case\">LPS<\/jats:styled-content> or CpG\u2010stimulated eosinophils respectively, <jats:styled-content style=\"fixed-case\">NK<\/jats:styled-content> cell recruitment was still observed alongside cytotoxicity and <jats:styled-content style=\"fixed-case\">IFN<\/jats:styled-content>\u03b3 production. CpG stimulation of eosinophils produced the pro\u2010inflammatory cytokine <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201012 and the chemokine <jats:styled-content style=\"fixed-case\">CXCL<\/jats:styled-content>10, which are important for <jats:styled-content style=\"fixed-case\">NK<\/jats:styled-content> cell activation and recruitment <jats:italic>in\u00a0vivo<\/jats:italic>. To demonstrate the importance of <jats:styled-content style=\"fixed-case\">CXCL<\/jats:styled-content>10 in <jats:styled-content style=\"fixed-case\">NK<\/jats:styled-content> cell recruitment, we found that CpG\u2010stimulated eosinophils pretreated with the gut microbial metabolite butyrate had reduced expression and production of <jats:styled-content style=\"fixed-case\">CXCL<\/jats:styled-content>10 and <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201012 and concomitantly were poor at recruitment of <jats:styled-content style=\"fixed-case\">NK<\/jats:styled-content> cells and inducing <jats:styled-content style=\"fixed-case\">IFN<\/jats:styled-content>\u03b3 in <jats:styled-content style=\"fixed-case\">NK<\/jats:styled-content> cells. Therefore, eosinophils like other innate immune cells of myeloid origin can conceivably stimulate <jats:styled-content style=\"fixed-case\">NK<\/jats:styled-content> cell activity. In addition, products of the gut microbiota can be potential inhibitors of <jats:styled-content style=\"fixed-case\">NK<\/jats:styled-content> cell.<\/jats:p>","DOI":"10.1111\/sji.12554","type":"journal-article","created":{"date-parts":[[2017,4,20]],"date-time":"2017-04-20T14:22:10Z","timestamp":1492698130000},"page":"417-424","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":20,"title":["<scp>TLR<\/scp>\u2010Stimulated Eosinophils Mediate Recruitment and Activation of <scp>NK<\/scp> Cells <i>In Vivo<\/i>"],"prefix":"10.1111","volume":"85","author":[{"given":"S. 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