Literature DB >> 11936363

Pathogenesis of septic shock: implications for prevention and treatment.

T Calandra1.   

Abstract

The innate immune system is in the vanguard of host defenses against infection. Recognition of invasive microbial pathogens is mediated by pattern recognition receptors on the surface of immune cells that recognize pathogen-associated molecular motifs. Considerable progress has been made in recent years in understanding how bacterial products initiate sepsis. In gram-negative sepsis, the LPS-binding protein (LBP), CD14 and the recently identified Toll-like receptor 4 (TLR4) are key molecules for the recognition of endotoxin (lipopolysaccharide, LPS) by cells of the myelomonocytic lineage. In gram-positive sepsis, components of the bacterial cell wall (peptidoglycan, PGN; lipoteichoic acids, LTA) have been shown to activate myeloid cells through an interaction with a receptor complex composed of CD14, TLR2 and perhaps also TLR6 (PGN) or CD14 and TLR4 (LTA). By contrast, gram-positive exotoxins act as superantigens and directly stimulate T lymphocytes by cross-linking the MHC class II of antigen presenting cells to specific chains of the T cell receptor. Immune cells activated by microbial pathogens release numerous effector molecules, which orchestrate the innate and adaptive host defenses. Furthermore, bacteria and microbial toxins directly activate the complement and coagulation systems, which play an important part in the host defensive response. Severe sepsis and septic shock can be viewed as clinical manifestations of a failing innate immune response that ultimately results in an overstimulation of the physiological host response. The pathogenesis of sepsis is far more complex that was initially anticipated. However, combined research efforts of basic scientists and clinical investigators continue to provide critical information for the identification of novel therapeutic targets. The exciting results obtained recently with treatment strategies designed to correct coagulation abnormalities occurring during sepsis are an example of how research may ultimately translate into improved patient care.

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Year:  2001        PMID: 11936363     DOI: 10.1179/joc.2001.13.Supplement-2.173

Source DB:  PubMed          Journal:  J Chemother        ISSN: 1120-009X            Impact factor:   1.714


  11 in total

Review 1.  Pathogenesis of sepsis: new concepts and implications for future treatment.

Authors:  Pierre-Yves Bochud; Thierry Calandra
Journal:  BMJ       Date:  2003-02-01

2.  Antigen capture of Porphyromonas gingivalis by human macrophages is enhanced but killing and antigen presentation are reduced by endotoxin tolerance.

Authors:  Manoj Muthukuru; Christopher W Cutler
Journal:  Infect Immun       Date:  2007-11-12       Impact factor: 3.441

Review 3.  Trauma-induced systemic inflammatory response versus exercise-induced immunomodulatory effects.

Authors:  Elvira Fehrenbach; Marion E Schneider
Journal:  Sports Med       Date:  2006       Impact factor: 11.136

4.  Post-ICU mortality in critically ill infected patients: an international study.

Authors:  Elie Azoulay; Corinne Alberti; Isabelle Legendre; Christian Brun Buisson; Jean Roger Le Gall
Journal:  Intensive Care Med       Date:  2004-11-04       Impact factor: 17.440

5.  Synergistic effects and antibiofilm properties of chimeric peptides against multidrug-resistant Acinetobacter baumannii strains.

Authors:  Ramamourthy Gopal; Young Gwon Kim; Jun Ho Lee; Seog Ki Lee; Jeong Don Chae; Byoung Kwan Son; Chang Ho Seo; Yoonkyung Park
Journal:  Antimicrob Agents Chemother       Date:  2013-12-23       Impact factor: 5.191

6.  Bone marrow stromal cells attenuate sepsis via prostaglandin E(2)-dependent reprogramming of host macrophages to increase their interleukin-10 production.

Authors:  Krisztián Németh; Asada Leelahavanichkul; Peter S T Yuen; Balázs Mayer; Alissa Parmelee; Kent Doi; Pamela G Robey; Kantima Leelahavanichkul; Beverly H Koller; Jared M Brown; Xuzhen Hu; Ivett Jelinek; Robert A Star; Eva Mezey
Journal:  Nat Med       Date:  2008-11-21       Impact factor: 53.440

7.  Alternative chemical modifications reverse the binding orientation of a pharmacophore scaffold in the active site of macrophage migration inhibitory factor.

Authors:  Gregg V Crichlow; Kai Fan Cheng; Darrin Dabideen; Mahendar Ochani; Bayan Aljabari; Valentin A Pavlov; Edmund J Miller; Elias Lolis; Yousef Al-Abed
Journal:  J Biol Chem       Date:  2007-05-25       Impact factor: 5.157

8.  WSES consensus conference: Guidelines for first-line management of intra-abdominal infections.

Authors:  Massimo Sartelli; Pierluigi Viale; Kaoru Koike; Federico Pea; Fabio Tumietto; Harry van Goor; Gianluca Guercioni; Angelo Nespoli; Cristian Tranà; Fausto Catena; Luca Ansaloni; Ari Leppaniemi; Walter Biffl; Frederick A Moore; Renato Poggetti; Antonio Daniele Pinna; Ernest E Moore
Journal:  World J Emerg Surg       Date:  2011-01-13       Impact factor: 5.469

9.  Efficient biosynthesis of a Cecropin A-melittin mutant in Bacillus subtilis WB700.

Authors:  Shengyue Ji; Weili Li; Abdul Rasheed Baloch; Meng Wang; Hengxin Li; Binyun Cao; Hongfu Zhang
Journal:  Sci Rep       Date:  2017-01-10       Impact factor: 4.379

Review 10.  Peptidoglycan in obligate intracellular bacteria.

Authors:  Christian Otten; Matteo Brilli; Waldemar Vollmer; Patrick H Viollier; Jeanne Salje
Journal:  Mol Microbiol       Date:  2017-12-12       Impact factor: 3.501

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