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Cecal Ligation and Puncture-induced Sepsis as a Model To Study Autophagy in Mice
Published on: February 9, 2014
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Inducing Experimental Polymicrobial Sepsis by Cecal Ligation and Puncture
Frances V Sjaastad1, Isaac J Jensen2, Roger R Berton2
1Microbiology, Immunology, and Cancer Biology Ph.D. Program, University of Minnesota, Minneapolis, Minnesota.
Current Protocols in Immunology
|October 7, 2020
Summary
The cecal ligation and puncture (CLP) mouse model effectively mimics human sepsis pathophysiology, including immune cell changes. This protocol details CLP surgery and immune analysis for sepsis research.
Area of Science:
- Preclinical sepsis research
- Immunology
- Surgical models
Background:
- Sepsis models include toxin administration, bacterial challenge, and barrier disruption.
- The cecal ligation and puncture (CLP) model simulates human sepsis with tissue necrosis and polymicrobial infection.
- CLP induces immune responses, including cell reduction and immunoparalysis, mirroring human sepsis.
Purpose of the Study:
- To detail the cecal ligation and puncture (CLP) surgical technique in mice.
- To outline methods for evaluating sepsis-induced immune system changes.
- To provide antibody panels for flow cytometry in septic mice.
Main Methods:
- Performing cecal ligation and puncture (CLP) as a survival surgical procedure.
- Analyzing physiological and biochemical responses post-CLP.
- Utilizing multiparameter flow cytometry with specific monoclonal antibody panels.
Main Results:
- The CLP model replicates key aspects of human sepsis, including hemodynamic and immune responses.
- Sepsis induction via CLP leads to transient immune cell reduction and prolonged immunoparalysis.
- This model facilitates understanding of immune system dynamics during sepsis.
Conclusions:
- The cecal ligation and puncture (CLP) model is a valuable tool for preclinical sepsis studies.
- Understanding immune system changes in CLP is crucial for sepsis research.
- Flow cytometry offers detailed analysis of immune responses in the septic host.

