IL-17 Receptor Signaling Is Required to Control Polymicrobial Sepsis
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
19/10/2012
19/10/2012
2009
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Resumo |
Sepsis is a systemic inflammatory response resulting from the inability of the host to contain the infection locally. Previously, we demonstrated that during severe sepsis there is a marked failure of neutrophil migration to the infection site, which contributes to dissemination of infection, resulting in high mortality. IL-17 plays an important role in neutrophil recruitment. Herein, we investigated the role of IL-17R signaling in polymicrobial sepsis induced by cecal ligation and puncture (CLP). It was observed that IL-17R-deficient mice, subjected to CLP-induced non-severe sepsis, show reduced neutrophil recruitment into the peritoneal cavity, spread of infection, and increased systemic inflammatory response as compared with C57BL/6 littermates. As a consequence, the mice showed an increased mortality rate. The ability of IL-17 to induce neutrophil migration was demonstrated in vivo and in vitro. Beside its role in neutrophil recruitment to the infection focus, IL-17 enhanced the microbicidal activity of the migrating neutrophils by a mechanism dependent on NO. Therefore, IL-17 plays a critical role in host protection during polymicrobial sepsis. The Journal of Immunology, 2009, 182: 7846-7854. FAPESP Fundacao de Amparo a Pesquisa do Estado de Sao Paulo CNPq Conselho Nacional de Pesquisa a Desenvolvimento Tecnologico |
Identificador |
JOURNAL OF IMMUNOLOGY, v.182, n.12, p.7846-7854, 2009 0022-1767 http://producao.usp.br/handle/BDPI/24174 10.4049/jimmunol.0803039 |
Idioma(s) |
eng |
Publicador |
AMER ASSOC IMMUNOLOGISTS |
Relação |
Journal of Immunology |
Direitos |
closedAccess Copyright AMER ASSOC IMMUNOLOGISTS |
Palavras-Chave | #COLONY-STIMULATING FACTOR #NITRIC-OXIDE PRODUCTION #NF-KAPPA-B #NEUTROPHIL MIGRATION #T-CELLS #IN-VIVO #SEPTIC SHOCK #INTERLEUKIN-17 FAMILY #CYTOKINE PRODUCTION #INDUCED ARTHRITIS #Immunology |
Tipo |
article original article publishedVersion |