Irradiation-induced pneumonitis mediated by the CD95/CD95-ligand system

J Natl Cancer Inst. 2006 Sep 6;98(17):1248-51. doi: 10.1093/jnci/djj335.

Abstract

Pneumonitis is a dose-limiting side effect of radiotherapy. However, the underlying mechanisms of irradiation-induced pneumonitis are unclear. Several observations suggest that the CD95/CD95-ligand (CD95L) system is involved in this process. Therefore, we examined the development of pneumonitis in CD95- and CD95L-deficient and wild-type mice after single irradiation with 0 or 12.5 Gy by measuring breathing frequency, pulmonary resistance, and histopathologic changes. Although wild-type mice developed pathognomonic alterations characteristic of pneumonitis (judged by alveolar wall thickness, interstitial edema, and interstitial and peribronchial inflammation) that paralleled increased breathing frequency ratio on days 5-70 (P < .03) with a maximum at day 37 (12.5 Gy, mean ratio = 1.05, 95% confidence interval [CI] = 1.01 to 1.08; P = .004 versus 0 Gy, mean ratio = 0.997, 95% CI = 0.976 to 1.02; P = .05) and pulmonary resistance (day 42, 12.5 Gy, mean = 0.51, 95% CI = 0.44 to 0.58 versus 0 Gy, mean = 0.40, 95% CI = 0.32 to 0.47; P = .03) after irradiation, no such changes were detected in CD95- or CD95L-deficient mice. This report demonstrates for the first time, to our knowledge, that the CD95/CD95L system is important for the development of irradiation-induced pneumonitis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Dose-Response Relationship, Radiation
  • Fas Ligand Protein
  • Female
  • Lung / metabolism
  • Lung / physiopathology
  • Lung / radiation effects*
  • Membrane Glycoproteins / deficiency
  • Membrane Glycoproteins / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Pneumonia / etiology*
  • Pneumonia / metabolism*
  • Pneumonia / physiopathology
  • Radiation Injuries / etiology*
  • Radiation Injuries / metabolism*
  • Radiation Injuries / physiopathology
  • Radiation, Ionizing
  • Radiotherapy / adverse effects
  • Radiotherapy / methods
  • Tumor Necrosis Factors / deficiency
  • Tumor Necrosis Factors / metabolism*

Substances

  • Fas Ligand Protein
  • Fasl protein, mouse
  • Membrane Glycoproteins
  • Tumor Necrosis Factors