Literature DB >> 21881397

Sepsis: the inflammatory foundation of pathophysiology and therapy.

Joan Li1, Brendan Carr, Munish Goyal, David F Gaieski.   

Abstract

Sepsis, defined as an infection accompanied by inflammation, is a complex disease process wherein the body's response to a pathogen is amplified far beyond the initial site of infection. The process begins when pathogen-associated molecular patterns on the bacteria or other pathogens induce an inflammatory cascade in the host. In the United States, it is estimated that every minute a patient with severe sepsis or septic shock presents to an emergency department and that > 751 000 cases of severe sepsis occur annually, resulting in an estimated 215 000 deaths. A rapid progression of illness severity from sepsis to severe sepsis to septic shock frequently occurs, driven by the body's inflammatory and anti-inflammatory responses to a pathogen, making sepsis a condition requiring timely intervention. The clinical management of severe sepsis and septic shock has evolved dramatically over the past decade and these new therapeutic approaches have been built on a deeper understanding of the natural evolution of sepsis. This article examines the underlying pathophysiological mechanisms of sepsis to help explain the clinical signs and symptoms manifested by severe sepsis patients. It also examines the significance of current proposed treatment strategies, including early goal-directed therapy, from a pathophysiological and inflammatory perspective.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21881397     DOI: 10.3810/hp.2011.08.585

Source DB:  PubMed          Journal:  Hosp Pract (1995)        ISSN: 2154-8331


  7 in total

1.  Pseudomonas aeruginosa and Its Bacterial Components Influence the Cytokine Response in Thymocytes and Splenocytes.

Authors:  Andreas Weber; Corinna Zimmermann; Anne K Mausberg; Thomas Dehmel; Bernd C Kieseier; Hans-Peter Hartung; Harald H Hofstetter
Journal:  Infect Immun       Date:  2016-04-22       Impact factor: 3.441

2.  Antibody WN1 222-5 mimics Toll-like receptor 4 binding in the recognition of LPS.

Authors:  Kathryn Gomery; Sven Müller-Loennies; Cory L Brooks; Lore Brade; Paul Kosma; Franco Di Padova; Helmut Brade; Stephen V Evans
Journal:  Proc Natl Acad Sci U S A       Date:  2012-11-26       Impact factor: 11.205

3.  Lymph node fibroblastic reticular cell transplants show robust therapeutic efficacy in high-mortality murine sepsis.

Authors:  Anne L Fletcher; Jessica S Elman; Jillian Astarita; Ryan Murray; Nima Saeidi; Joshua D'Rozario; Konstantin Knoblich; Flavian D Brown; Frank A Schildberg; Janice M Nieves; Tracy S P Heng; Richard L Boyd; Shannon J Turley; Biju Parekkadan
Journal:  Sci Transl Med       Date:  2014-08-13       Impact factor: 17.956

4.  Structural Basis for Antibody Recognition of Lipid A: INSIGHTS TO POLYSPECIFICITY TOWARD SINGLE-STRANDED DNA.

Authors:  Omid Haji-Ghassemi; Sven Müller-Loennies; Teresa Rodriguez; Lore Brade; Paul Kosma; Helmut Brade; Stephen V Evans
Journal:  J Biol Chem       Date:  2015-06-17       Impact factor: 5.157

5.  The Combining Sites of Anti-lipid A Antibodies Reveal a Widely Utilized Motif Specific for Negatively Charged Groups.

Authors:  Omid Haji-Ghassemi; Sven Müller-Loennies; Teresa Rodriguez; Lore Brade; Hans-Dieter Grimmecke; Helmut Brade; Stephen V Evans
Journal:  J Biol Chem       Date:  2016-03-01       Impact factor: 5.157

6.  T cell activation status determines the cytokine pattern induced by zymosan and bacterial DNA both in thymocytes and splenocytes.

Authors:  C Zimmermann; A Weber; A K Mausberg; B C Kieseier; H P Hartung; H H Hofstetter
Journal:  Clin Exp Immunol       Date:  2013-05       Impact factor: 4.330

Review 7.  Coordinated Molecular Cross-Talk between Staphylococcus aureus, Endothelial Cells and Platelets in Bloodstream Infection.

Authors:  Carolina D Garciarena; Tony M McHale; Rebecca L Watkin; Steven W Kerrigan
Journal:  Pathogens       Date:  2015-12-05
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.