Post-mortem markers of sepsis: an immunohistochemical study using VLA-4 (CD49d/CD29) and ICAM-1 (CD54) for the detection of sepsis-induced lung injury

Int J Legal Med. 2001;114(4-5):291-4. doi: 10.1007/s004140000172.

Abstract

The up-regulation of different adhesion molecules such as VLA-4 (CD49d/CD29) and ICAM-1 (CD54) on the pulmonary endothelium and leukocytes, is a key event in sepsis-induced lung injury leading to inflammatory tissue alterations. The value of VLA-4 and ICAM-1 as micromorphological post-mortem markers for the detection of sepsis-induced lung injury, was evaluated in a semiquantitative immunohistochemical study. VLA-4 was strongly expressed on intravascular, interstitial and intra-alveolar leukocytes in sepsis-associated fatalities, whereas in non-septic fatalities an irregular weak immunoreactivity was observed on interstitial leukocytes and no positive immunohistochemical expression was detected on intravascular or intra-alveolar leukocytes. ICAM-1 was strongly expressed on endothelial cells of the pulmonary microvasculature and on pulmonary macrophages and lymphocytes in sepsis-associated fatalities. In contrast, an infrequent weak immunohistochemical reaction for ICAM-1 was found on pulmonary endothelium and on perivascular leukocytes in non-septic fatalities. Based on the results of the present preliminary study, VLA-4 and ICAM-1 can be considered as useful immunohistochemical post-mortem markers of sepsis.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Autopsy / methods*
  • Biomarkers
  • Case-Control Studies
  • Cell Adhesion Molecules / metabolism
  • Female
  • Humans
  • Immunohistochemistry
  • Integrin alpha4beta1
  • Integrin beta1 / metabolism*
  • Integrins / metabolism*
  • Intercellular Adhesion Molecule-1 / metabolism*
  • Male
  • Middle Aged
  • Receptors, Lymphocyte Homing / metabolism*
  • Respiratory Distress Syndrome / etiology
  • Respiratory Distress Syndrome / metabolism
  • Statistics, Nonparametric
  • Systemic Inflammatory Response Syndrome / complications
  • Systemic Inflammatory Response Syndrome / metabolism
  • Systemic Inflammatory Response Syndrome / pathology*

Substances

  • Biomarkers
  • Cell Adhesion Molecules
  • Integrin alpha4beta1
  • Integrin beta1
  • Integrins
  • Receptors, Lymphocyte Homing
  • Intercellular Adhesion Molecule-1