STAT4 is required for antibacterial defense but enhances mortality during polymicrobial sepsis

CJ Godshall, AB Lentsch, JC Peyton… - Clinical Diagnostic …, 2001 - Am Soc Microbiol
CJ Godshall, AB Lentsch, JC Peyton, MJ Scott, WG Cheadle
Clinical Diagnostic Laboratory Immunology, 2001Am Soc Microbiol
The signal transducer and activator of transcription factor 4 (STAT4) pathway mediates the
intracellular effects of interleukin-12 (IL-12), leading to the production of gamma interferon,
induction of a T helper type 1 response, and increased natural killer cell cytotoxicity. The
purpose of this study was to determine the role of the STAT4 pathway during polymicrobial
peritonitis in the cecal ligation and puncture (CLP) model. CLP was performed on STAT4-
deficient (STAT4−/−) and wild-type control (BALB/c) mice. At 4 h after CLP, STAT4−/− mice …
Abstract
The signal transducer and activator of transcription factor 4 (STAT4) pathway mediates the intracellular effects of interleukin-12 (IL-12), leading to the production of gamma interferon, induction of a T helper type 1 response, and increased natural killer cell cytotoxicity. The purpose of this study was to determine the role of the STAT4 pathway during polymicrobial peritonitis in the cecal ligation and puncture (CLP) model. CLP was performed on STAT4-deficient (STAT4−/−) and wild-type control (BALB/c) mice. At 4 h after CLP, STAT4−/− mice had significantly higher bacterial counts in the peritoneal lavage fluid, liver, and blood. This difference persisted for 18 h in the peritoneal lavage fluid and blood. Neutrophil migration to the site of infection and into remote tissues was unaffected. Despite higher bacterial counts locally and systemically, STAT4−/− mice had a lower mortality rate than BALB/c controls. In contrast, blockade of IL-12 in BALB/c mice was detrimental to host survival. A blunted serum IL-12 response at 18 h after CLP was exhibited in STAT4−/− mice. These results suggest several critical roles for the STAT4 pathway in the resolution of polymicrobial infections. Additionally, the disparate effects observed with IL-12 blockade and STAT4 deficiency on host survival suggest that IL-12 may activate alternate pathways promoting survival.
American Society for Microbiology