» Articles » PMID: 24351718

Towards Clinical Applications of Anti-endotoxin Antibodies; a Re-appraisal of the Disconnect

Overview
Journal Toxins (Basel)
Publisher MDPI
Specialty Toxicology
Date 2013 Dec 20
PMID 24351718
Citations 11
Authors
Affiliations
Soon will be listed here.
Abstract

Endotoxin is a potent mediator of a broad range of patho-physiological effects in humans. It is present in all Gram negative (GN) bacteria. It would be expected that anti-endotoxin therapies, whether antibody based or not, would have an important adjuvant therapeutic role along with antibiotics and other supportive therapies for GN infections. Indeed there is an extensive literature relating to both pre-clinical and clinical studies of anti-endotoxin antibodies. However, the extent of disconnect between the generally successful pre-clinical studies versus the failures of the numerous large clinical trials of antibody based and other anti-endotoxin therapies is under-appreciated and unexplained. Seeking a reconciliation of this disconnect is not an abstract academic question as clinical trials of interventions to reduce levels of endotoxemia levels are ongoing. The aim of this review is to examine new insights into the complex relationship between endotoxemia and sepsis in an attempt to bridge this disconnect. Several new factors to consider in this reappraisal include the frequency and types of GN bacteremia and the underlying mortality risk in the various study populations. For a range of reasons, endotoxemia can no longer be considered as a single entity. There are old clinical trials which warrant a re-appraisal in light of these recent advances in the understanding of the structure-function relationship of endotoxin. Fundamentally however, the disconnect not only remains, it has enlarged.

Citing Articles

Efficacy and safety of phospholipid nanoparticles (VBI-S) in reversing intractable hypotension in patients with septic shock: a multicentre, open-label, repeated measures, phase 2a clinical pilot trial.

Simpkins C, Moncure M, Klepacz H, Roach K, Benzaquen S, Diaz-Caballero L EClinicalMedicine. 2024; 68:102430.

PMID: 38545092 PMC: 10965406. DOI: 10.1016/j.eclinm.2024.102430.


The role of endotoxin in septic shock.

Kellum J, Ronco C Crit Care. 2023; 27(1):400.

PMID: 37858258 PMC: 10585761. DOI: 10.1186/s13054-023-04690-5.


Intracellular and Extracellular Lipopolysaccharide Signaling in Sepsis: Avenues for Novel Therapeutic Strategies.

Gabarin R, Li M, Zimmel P, Marshall J, Li Y, Zhang H J Innate Immun. 2021; 13(6):323-332.

PMID: 34004605 PMC: 8613564. DOI: 10.1159/000515740.


Help is on the way: Monoclonal antibody therapy for multi-drug resistant bacteria.

Babb R, Pirofski L Virulence. 2017; 8(7):1055-1058.

PMID: 28306387 PMC: 5711430. DOI: 10.1080/21505594.2017.1306620.


Endotoxin neutralization by an O-antigen specific monoclonal antibody: A potential novel therapeutic approach against Klebsiella pneumoniae ST258.

Szijarto V, Guachalla L, Hartl K, Varga C, Badarau A, Mirkina I Virulence. 2017; 8(7):1203-1215.

PMID: 28103139 PMC: 5711440. DOI: 10.1080/21505594.2017.1279778.


References
1.
Werdan K, Pilz G, Bujdoso O, Fraunberger P, Neeser G, Schmieder R . Score-based immunoglobulin G therapy of patients with sepsis: the SBITS study. Crit Care Med. 2007; 35(12):2693-2701. View

2.
Hoffman W, Pollack M, Banks S, Koev L, Solomon M, Danner R . Distinct functional activities in canine septic shock of monoclonal antibodies specific for the O polysaccharide and core regions of Escherichia coli lipopolysaccharide. J Infect Dis. 1994; 169(3):553-61. DOI: 10.1093/infdis/169.3.553. View

3.
Maeshima N, Fernandez R . Recognition of lipid A variants by the TLR4-MD-2 receptor complex. Front Cell Infect Microbiol. 2013; 3:3. PMC: 3569842. DOI: 10.3389/fcimb.2013.00003. View

4.
Opal S, Palardy J, Marra M, Fisher Jr C, McKelligon B, Scott R . Relative concentrations of endotoxin-binding proteins in body fluids during infection. Lancet. 1994; 344(8920):429-31. DOI: 10.1016/s0140-6736(94)91767-1. View

5.
Levi M, ten Cate H, Bauer K, van der Poll T, Edgington T, Buller H . Inhibition of endotoxin-induced activation of coagulation and fibrinolysis by pentoxifylline or by a monoclonal anti-tissue factor antibody in chimpanzees. J Clin Invest. 1994; 93(1):114-20. PMC: 293743. DOI: 10.1172/JCI116934. View