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Published on: April 11, 2012
E5 monoclonal immunoglobulin M antibody for the treatment of gram-negative sepsis
1Department of Pharmacy Practice, College of Pharmacy, University of Arkansas for Medical Sciences, Little Rock 72205.
Abstract:
Despite the advent of aminoglycoside and beta-lactam antibiotics and early antimicrobial intervention, overall morbidity and mortality associated with gram-negative sepsis and bacteremia remain high. Complications of sepsis have been related to the release of endotoxin from the cell walls of gram-negative bacilli. Although antibiotics can effectively kill gram-negative bacteria, they have no effect on lipopolysaccharide lipopolysaccharide (LPS) and may, in fact, enhance its release when cell lysis occurs. Lipid A, the lipid portion of LPS, is composed of glucosamines, polar phosphate groups, and fatty acids. It represents the endotoxic component of gram-negative bacteria and is responsible for host responses to LPS, including fever, hypotension, and shock. E5 is a murine monoclonal immunoglobulin M antibody directed against the lipid A portion of the cell-wall endotoxin that is common to clinically important gram-negative bacilli. A clinical evaluation program of E5 included patients who were moderately to severely ill with clinical evidence of an infection usually caused by gram-negative bacteria. In pharmacokinetic and safety studies, laboratory tests revealed no evidence of antibody-mediated toxicity and serum antibody concentrations in the desired therapeutic range (greater than 5 microgramS/mL) were found as late as 72 hours after initial infusion of E5. In a Phase II study, mortality rates at seven days in patients with documented gram-negative infection were 22 percent in the placebo group compared with 7 percent in the E5-treated groups.(ABSTRACT TRUNCATED AT 250 WORDS)
Insights
A novel antibody, E5, targeting gram-negative bacteria endotoxin
Area of Science:
- Microbiology
- Immunology
- Pharmacology
Background:
- Gram-negative bacterial infections, including sepsis and bacteremia, present significant morbidity and mortality.
- Antibiotics are limited in treating endotoxin release, a key sepsis complication.
- Lipid A, the endotoxic component of lipopolysaccharide (LPS), drives severe host responses.
Purpose of the Study:
- To evaluate the safety and efficacy of E5, a murine monoclonal antibody targeting gram-negative bacterial endotoxin's Lipid A component.
- To assess E5's pharmacokinetic profile and therapeutic potential in patients with gram-negative infections.
Main Methods:
- A clinical evaluation program involving moderately to severely ill patients with gram-negative infections.
- Pharmacokinetic and safety studies to determine antibody levels and toxicity.
- A Phase II clinical trial comparing E5 treatment to a placebo.
Main Results:
- E5 demonstrated no antibody-mediated toxicity in laboratory tests.
- Therapeutic serum antibody concentrations of E5 were maintained for up to 72 hours.
- Mortality rates at seven days were significantly lower in the E5-treated group (7%) compared to the placebo group (22%).
Conclusions:
- E5 is a safe and potentially effective therapeutic agent against gram-negative bacterial infections.
- Targeting Lipid A with monoclonal antibody E5 shows promise in reducing sepsis-related mortality.

