Related Experiment Video
Updated: Aug 15, 2026

Colon Ascendens Stent Peritonitis (CASP) - a Standardized Model for Polymicrobial Abdominal Sepsis
Published on: December 18, 2010
IC14, a CD14 specific monoclonal antibody, is a potential treatment for patients with severe sepsis
Abstract:
CD14 is a pattern recognition receptor for the bacterial cell wall components from Gram-positive and Gram-negative bacteria as well as mycobacteria. Binding of lipopolysaccharide (LPS) or other cell wall constituents to CD14 initiates signal transduction through the Toll-like receptors resulting in the release of pro-inflammatory cytokines and the initiation of the systemic inflammatory response. In rabbits and non-human primates, CD14 specific antibodies were shown to attenuate responses to LPS or Escherichia coli challenge including pro-inflammatory cytokine release, acute lung injury, hypotension and changes in lung, liver, spleen and adrenal gland morphology. In healthy human subjects, single doses of a chimeric CD14 antibody (IC14) have been shown to be well tolerated and result in a dose-related degree of saturation of CD14 receptors on monocytes and granulocytes. Pretreatment of healthy subjects with IC14 2 h prior to LPS resulted in an attenuation of the LPS-induced fever, clinical symptoms, and leukocyte activation and degranulation. IC14 inhibited the release of TNF-alpha, IL-6, and IL-10 and delayed the release of sTNFR(I) and IL-1ra. Further studies are in progress to characterize the safety and clinical pharmacology of IC14 in patients with severe sepsis.
Insights
A CD14 antibody (IC14) effectively blocks bacterial component responses in humans, reducing inflammation and symptoms. This antibody shows promise for treating severe sepsis by targeting CD14 receptors.
Area of Science:
- Immunology
- Microbiology
- Pharmacology
Background:
- CD14 acts as a pattern recognition receptor for bacterial cell wall components.
- CD14 binding initiates Toll-like receptor signaling, leading to pro-inflammatory cytokine release and systemic inflammation.
Purpose of the Study:
- To evaluate the safety and efficacy of a chimeric CD14 antibody (IC14) in humans.
- To assess IC14's ability to block lipopolysaccharide (LPS)-induced inflammatory responses.
Main Methods:
- Administration of single doses of IC14 to healthy human subjects.
- Pretreatment with IC14 followed by LPS challenge.
- Measurement of CD14 receptor saturation, cytokine release, and clinical symptoms.
Main Results:
- IC14 was well tolerated and saturated CD14 receptors in a dose-dependent manner.
- IC14 pretreatment attenuated LPS-induced fever, clinical symptoms, and leukocyte activation.
- IC14 inhibited key pro-inflammatory cytokines (TNF-alpha, IL-6) and modulated other inflammatory mediators.
Conclusions:
- IC14 demonstrates safety and efficacy in blocking CD14-mediated inflammatory responses in humans.
- IC14 holds potential for managing severe sepsis and other inflammatory conditions.
- Further clinical studies are underway to confirm IC14's therapeutic value in sepsis patients.

