Increased expression of human leukocyte antigen-DR on pulmonary macrophages in bronchopulmonary dysplasia

J D Jacobson1, W E Truog, D R Benjamin

  • 1Developmental Endocrinology Branch, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892.

Pediatric Research
|September 1, 1993
PubMed

Insights

Macrophages expressing HLA-DR are elevated in infants with bronchopulmonary dysplasia. This immune marker suggests increased pulmonary inflammation in this condition, unlike infant respiratory distress syndrome.

Area of Science:

  • Immunology
  • Pulmonary Medicine
  • Pathology

Background:

  • Bronchopulmonary dysplasia (BPD) is a chronic lung disease in infants.
  • Pulmonary inflammation plays a role in BPD pathogenesis.
  • Human Leukocyte Antigen - antigen D Related (HLA-DR) is an immune activation marker.

Purpose of the Study:

  • To investigate the expression of HLA-DR on pulmonary tissue in patients with BPD.
  • To compare HLA-DR expression in BPD patients with control groups.

Main Methods:

  • Autopsy pulmonary tissue samples were analyzed using the immunoperoxidase method.
  • HLA-DR expression was assessed on macrophages and endothelial cells.
  • Quantification involved counting positive and total macrophages/monocytes per high power field.

Main Results:

  • HLA-DR expression was exclusively observed on macrophages, not pulmonary endothelial cells.
  • Patients with BPD showed significantly higher numbers of total and HLA-DR-positive macrophages (p < 0.05).
  • The percentage of HLA-DR-positive macrophages was also significantly higher in BPD patients (p < 0.005).
  • No significant difference in total macrophages was found in infant respiratory distress syndrome patients compared to controls.

Conclusions:

  • Increased pulmonary macrophages expressing HLA-DR indicate heightened immune activation in bronchopulmonary dysplasia.
  • This finding suggests a role for macrophage-mediated inflammation in BPD.
  • Infant respiratory distress syndrome did not show similar alterations in macrophage counts.