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10.1038/mi.2016.80

http://scihub22266oqcxt.onion/10.1038/mi.2016.80
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C5350071!5350071!27624780
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suck abstract from ncbi


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pmid27624780      Mucosal+Immunol 2017 ; 10 (3): 673-84
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  • IL-17A-mediated neutrophil recruitment limits expansion of segmented filamentous bacteria #MMPMID27624780
  • Flannigan KL; Ngo VL; Geem D; Harusato A; Hirota SA; Parkos CA; Lukacs NW; Nusrat A; Gaboriau-Routhiau V; Cerf-Bensussan N; Gewirtz AT; Denning TL
  • Mucosal Immunol 2017[May]; 10 (3): 673-84 PMID27624780show ga
  • Specific components of the intestinal microbiota are capable of influencing immune responses such that a mutualistic relationship is established. In mice, colonization with segmented filamentous bacteria (SFB) induces Th17 cell differentiation in the intestine, yet the effector functions of IL-17A in response to SFB remain incompletely understood. Here, we report that colonization of mice with SFB-containing microbiota induced IL-17A- and CXCR2-dependent recruitment of neutrophils to the ileum. This response required adaptive immunity as Rag-deficient mice colonized with SFB-containing microbiota failed to induce IL-17A, CXCL1 and CXCL2, and displayed defective neutrophil recruitment to the ileum. Interestingly, neutrophil depletion in wild-type mice resulted in significantly augmented Th17 responses and SFB expansion, which correlated with impaired expression of IL-22 and antimicrobial peptides. These data provide novel insight into a dynamic IL-17A-CXCR2-neutrophil axis during acute SFB colonization and demonstrate a central role for neutrophils in limiting SFB expansion.
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