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Publication : TREM-1 promotes survival during septic shock in mice.

First Author  Gibot S Year  2007
Journal  Eur J Immunol Volume  37
Issue  2 Pages  456-66
PubMed ID  17230441 Mgi Jnum  J:117877
Mgi Id  MGI:3697944 Doi  10.1002/eji.200636387
Citation  Gibot S, et al. (2007) TREM-1 promotes survival during septic shock in mice. Eur J Immunol 37(2):456-66
abstractText  Triggering receptor expressed on myeloid (TREM)-1 is integral to the inflammatory response occurring during septic shock, although its precise function has yet to be determined. Here we show that in vivo silencing of TREM-1 using siRNA duplexes in a fecal peritonitis mouse model resulted in a blunted inflammatory response and increased mortality. This was associated with impaired bacterial clearance related to marked inhibition of the neutrophil oxidative burst. By contrast, TREM-1-silenced mice were highly resistant to a lethal endotoxin challenge, while partial silencing of TREM-1 in the bacterial peritonitis model produced a significant survival benefit. These data highlight the crucial role of the TREM-1 pathway in mounting an adequate inflammatory and cytotoxic response to polymicrobial sepsis, and both the therapeutic promise and potential risks of its modulation.
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