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

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.

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