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

      review-article
      1 , 2 , 3
      Toxins
      MDPI
      endotoxin, endotoxemia, anti-endotoxin antibodies, sepsis, polymyxin, Gram-negative bacteria

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          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.

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          Most cited references165

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          Lipid A modification systems in gram-negative bacteria.

          The lipid A moiety of lipopolysaccharide forms the outer monolayer of the outer membrane of most gram-negative bacteria. Escherichia coli lipid A is synthesized on the cytoplasmic surface of the inner membrane by a conserved pathway of nine constitutive enzymes. Following attachment of the core oligosaccharide, nascent core-lipid A is flipped to the outer surface of the inner membrane by the ABC transporter MsbA, where the O-antigen polymer is attached. Diverse covalent modifications of the lipid A moiety may occur during its transit from the outer surface of the inner membrane to the outer membrane. Lipid A modification enzymes are reporters for lipopolysaccharide trafficking within the bacterial envelope. Modification systems are variable and often regulated by environmental conditions. Although not required for growth, the modification enzymes modulate virulence of some gram-negative pathogens. Heterologous expression of lipid A modification enzymes may enable the development of new vaccines.
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            LPS, TLR4 and infectious disease diversity.

            Innate immune receptors recognize microorganism-specific motifs. One such receptor-ligand complex is formed between the mammalian Toll-like receptor 4 (TLR4)-MD2-CD14 complex and bacterial lipopolysaccharide (LPS). Recent research indicates that there is significant phylogenetic and individual diversity in TLR4-mediated responses. In addition, the diversity of LPS structures and the differential recognition of these structures by TLR4 have been associated with several bacterial diseases. This review will examine the hypothesis that the variability of bacterial ligands such as LPS and their innate immune receptors is an important factor in determining the outcome of infectious disease.
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              Novel strategies for the treatment of sepsis.

              The history of therapeutic interventions in clinical trials for sepsis has been referred to as the "graveyard for pharmaceutical companies." That is now set to change, as research provides hope for new approaches that will be therapeutically effective in humans with sepsis.
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                Author and article information

                Journal
                Toxins (Basel)
                Toxins (Basel)
                toxins
                Toxins
                MDPI
                2072-6651
                18 December 2013
                December 2013
                : 5
                : 12
                : 2589-2620
                Affiliations
                [1 ]Rural Health Academic Center, Melbourne Medical School, University of Melbourne, Parkville 3010, Australia
                [2 ]Division of Internal Medicine, Ballarat Health Services, Ballarat 3350, Australia; E-Mail: jamesh@ 123456bhs.org.au ; Tel.: +61-3-5320-4322; Fax: +61-3-53-206500
                [3 ]Infection Control Committees, St John of God Hospital and Ballarat Health Services, Ballarat 3353, Australia
                Article
                toxins-05-02589
                10.3390/toxins5122589
                3873702
                24351718
                c5e8d468-7de7-485e-b18e-ebe4f9ce224c
                © 2013 by the authors; licensee MDPI, Basel, Switzerland.

                This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license ( http://creativecommons.org/licenses/by/3.0/).

                History
                : 31 October 2013
                : 09 December 2013
                : 13 December 2013
                Categories
                Review

                endotoxin,endotoxemia,sepsis,polymyxin,anti-endotoxin antibodies,gram-negative bacteria

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