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Colon Ascendens Stent Peritonitis (CASP) - a Standardized Model for Polymicrobial Abdominal Sepsis
Published on: December 18, 2010
TAKEDA-143242 increased survival via reduced cytokines in porcine peritonitis
Roy D Goldfarb1, John W Ortegel, Joseph E Parrillo
1Department of Medicine, Sections of Cardiology and Critical Care, Rush Medical College, Chicago, Illinois, USA. Roy.d.goldfarb@umdnj.edu
Abstract:
TAKEDA-143242 (TAK-242) is a small molecule shown to inhibit lipopolysaccharide-induced intracellular signaling and inflammation. In vitro studies demonstrated that TAK-242 can prevent release of TNF-α, IL-1β, and IL-6 from activated macrophages of several species, including pigs. This study tested the hypothesis that TAK-242 would protect pigs from lethal gram-negative peritonitis via an anti-cytokine mechanism. A validated model of porcine gram-negative peritonitis, which employs chronically inplantated cardiac transducers and aortic and pulmonary artery catheters, was used. Pigs were pretreated with TAK-242 or its vehicle via a blinding procedure prior to intraperitoneal implantation of an LD(90) dose of E. coli 0111:B4 in a fibrin clot. Ten pigs were treated with TAK-242 and nine with its vehicle. All ten TAK-242 treated pigs survived, while three of the nine vehicle treated pigs survived (P = 0.01 χ(2) test). Pulmonary artery pressure increased markedly in vehicle pigs, and this elevation was significantly (two-way ANOVA) obviated in TAK-242 treated group. Circulating levels of cytokines in vehicle treated pigs showed increased expression (3930 ± 1770 at 1 h, 1007 ± 400 TNF-α at 2 h; 719 ± 308 of IL-1β at 2-6 h; 33000 ± 1000 of IL-6 at 2-4 h [pg/mL, mean ± SEM]). Peak circulating levels of these cytokines were significantly reduced by pretreatment with TAK-242 (<25 pg/mL TNF-α ; <100 pg/mL IL-1β; 0-1700 pg/mL IL-6, peak values). This study found that pretreatment with TAK-242 yielded significantly positive survival benefit in a lethal sepsis model that was associated with improved cardiovascular status and suppressed cytokine release.
Insights
TAKEDA-143242 (TAK-242) significantly improved survival in pigs with lethal gram-negative peritonitis. This small molecule inhibited inflammatory cytokine release and improved cardiovascular function during sepsis.
Area of Science:
- Immunology
- Pharmacology
- Critical Care Medicine
Background:
- Lipopolysaccharide (LPS) triggers intracellular signaling pathways, leading to inflammation and cytokine release.
- TAKEDA-143242 (TAK-242) is a small molecule inhibitor of LPS-induced signaling and inflammation.
- TAK-242 has demonstrated in vitro efficacy in preventing pro-inflammatory cytokine release from activated macrophages.
Purpose of the Study:
- To evaluate the efficacy of TAK-242 in a porcine model of lethal gram-negative peritonitis.
- To determine if TAK-242 protects against sepsis-induced mortality via an anti-cytokine mechanism.
Main Methods:
- A validated porcine model of gram-negative peritonitis using intraperitoneal E. coli 0111:B4 implantation.
- Pigs were pretreated with TAK-242 or vehicle control under blinded conditions.
- Hemodynamic parameters (pulmonary artery pressure) and circulating cytokine levels (TNF-α, IL-1β, IL-6) were monitored.
Main Results:
- TAK-242 pretreatment resulted in significantly higher survival rates (100% vs. 33.3% in vehicle group, P = 0.01).
- TAK-242 significantly attenuated the increase in pulmonary artery pressure observed in vehicle-treated pigs.
- Circulating levels of TNF-α, IL-1β, and IL-6 were significantly reduced in the TAK-242 treated group compared to controls.
Conclusions:
- Pretreatment with TAK-242 confers a significant survival benefit in a lethal model of porcine gram-negative peritonitis.
- The protective effect of TAK-242 is associated with suppressed cytokine release and improved cardiovascular stability.
- TAK-242 demonstrates potential as a therapeutic agent for sepsis by inhibiting key inflammatory mediators.
