IL-17 Receptor Signaling Is Required to Control Polymicrobial Sepsis


Autoria(s): FREITAS, Andressa; ALVES-FILHO, Jose C.; VICTONI, Tatiana; SECHER, Thomas; LEMOS, Henrique P.; SONEGO, Fabiane; CUNHA, Fernando Q.; RYFFEL, Bernhard
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2009

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

http://dx.doi.org/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