IL-5 in post-traumatic eosinophilic pleural effusion

Clin Exp Immunol. 1993 Jul;93(1):115-9. doi: 10.1111/j.1365-2249.1993.tb06506.x.

Abstract

Thoracic trauma or pneumothorax can result in pleural fluid eosinophilia. In this study we investigated the role of the eosinophilopoietic cytokine IL-5 in three cases of post-traumatic eosinophilic pleural effusions (EPE). Using a specific immunoenzymatic assay, significant levels of IL-5 were found in EPE (range 100-3000 pg/ml), while IL-5 was undetectable (< 25 pg/ml) in corresponding serum samples and in non-eosinophilic pleural fluids. IL-5 present in pleural fluids was found bioactive in a proliferative assay using a mouse CTLL-2 cell line transfected with the cDNA corresponding to the alpha chain of the human IL-5 receptor. Using a reverse polymerase chain reaction (PCR) method, we found IL-5 mRNA expression within pleural mononuclear cells from patients with EPE, but not in corresponding peripheral blood mononuclear cells (PBMC), confirming that IL-5 is synthesized locally in the pleural cavity. In the two cases in which pleural CD4+ cells were purified, these cells were identified as the major source of IL-5. Taken together, these data indicate that the development of post-traumatic EPE is related to a local secretion of IL-5 by CD4+ cells present in the pleural cavity.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Base Sequence
  • CD4-Positive T-Lymphocytes / immunology
  • Cell Line
  • Female
  • Gene Expression
  • Humans
  • Immunoenzyme Techniques
  • Interleukin-5 / biosynthesis*
  • Interleukin-5 / genetics
  • Male
  • Middle Aged
  • Molecular Sequence Data
  • Pleural Effusion / etiology
  • Pleural Effusion / immunology*
  • Pneumothorax / complications
  • Polymerase Chain Reaction
  • Pulmonary Eosinophilia / etiology
  • Pulmonary Eosinophilia / immunology*
  • RNA, Messenger / analysis
  • Thoracic Injuries / complications

Substances

  • Interleukin-5
  • RNA, Messenger