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A more recent version of this article appeared on January 1, 2007

Published online before print October 4, 2006
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© by The Society for Leukocyte Biology
Journal of Leukocyte Biology, doi:10.1189/jlb.0806542


Received for publication August 31, 2006.

Accepted for publication September 1, 2006.


Article

The disconnect between animal models of sepsis and human sepsis

Daniel Rittirsch , L. Marco Hoesel , and Peter A. Ward @

Department of Pathology, University of Michigan Medical School, Ann Arbor, Michigan, USA

@ To whom correspondence should be addressed. E-mail: pward{at}umich.edu.


   Abstract

Frequently used experimental models of sepsis include cecal ligation and puncture, ascending colon stent peritonitis, and the i.p. or i.v. injection of bacteria or bacterial products (such as LPS). Many of these models mimic the pathophysiology of human sepsis. However, identification of mediators in animals, the blockade of which has been protective, has not translated into clinical efficacy in septic humans. We describe the shortcomings of the animal models and reasons why effective therapy for human sepsis cannot be derived readily from promising findings in animal sepsis.

Key Words: cecal ligation and puncture • lipopolysaccharide • rodents




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