Leukocyte-endothelial interactions via ICAM-1 are detrimental in polymicrobial sepsis

Martijn van Griensven1, Christian Probst, Katrin Müller

  • 1Ludwig Boltzmann Institute for Experimental and Clinical Traumatology, Donaueschingenstrasse 13, A-1200 Vienna, Austria. Martijn.van.Griensven@ibitrauma.org

Shock (Augusta, Ga.)
|March 23, 2006
PubMed

Insights

Mice lacking the ICAM-1 gene showed significantly reduced mortality in a sepsis model. This was linked to lower immune cell activity and inflammatory markers, suggesting ICAM-1 plays a key role in sepsis severity.

Area of Science:

  • Immunology
  • Pathophysiology
  • Sepsis Research

Background:

  • Intercellular Adhesion Molecule 1 (ICAM-1) is crucial for leukocyte transmigration in sepsis.
  • Leukocyte transmigration correlates with multi-organ failure severity.
  • The role of ICAM-1 gene deletion in polymicrobial sepsis requires further investigation.

Purpose of the Study:

  • To investigate the impact of ICAM-1 gene deletion on mortality and immune responses in a murine model of polymicrobial sepsis.
  • To evaluate the effect of ICAM-1 deficiency on leukocyte subpopulations, cytokine levels, and organ damage.

Main Methods:

  • A cecal ligation and puncture (CLP) sepsis model was used in ICAM-1 knockout (KO) and wild-type (WT) mice.
  • Mortality, body weight, temperature, delayed-type hypersensitivity (DTH) reaction, lymphocyte subpopulations, and cytokine levels were measured.
  • Histological examination of liver and lung tissues was performed.

Main Results:

  • Mortality was significantly lower in ICAM-1 KO mice compared to WT mice (5% vs 45.0%).
  • KO mice exhibited reduced lymphocyte subpopulations (CD4, CD8, NK cells) and lower levels of pro-inflammatory cytokines (TNF-alpha, IL-1beta, IL-6, IL-10).
  • Histology revealed less leukocyte invasion and organ damage in KO mice, with a decreased DTH reaction.

Conclusions:

  • ICAM-1 gene deletion significantly reduces mortality in a murine sepsis model.
  • The reduced mortality is associated with an attenuated immune response, including decreased lymphocyte counts, cytokine levels, and DTH reaction.
  • These findings highlight ICAM-1's critical role in sepsis pathogenesis and suggest it as a potential therapeutic target.

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