Adenovirus-mediated granulocyte-macrophage colony-stimulating factor improves lung pathology of pulmonary alveolar proteinosis in granulocyte-macrophage colony-stimulating factor-deficient mice

Hum Gene Ther. 1998 Sep 20;9(14):2101-9. doi: 10.1089/hum.1998.9.14-2101.

Abstract

Mutation of the granulocyte-macrophage colony-stimulating factor (GM-CSF) gene by homologous recombination causes progressive pulmonary alveolar proteinosis (PAP) in GM-CSF-deficient mice (GM-/-). The present study tested whether adenovirus-mediated expression of GM-CSF alters the progression of PAP in GM-/- mice. Adult mice were pretreated with an anti-T cell receptor (TCR) antibody to block T cell-mediated immune response, followed by intratracheal instillation of deltaE1-E3 replication-deficient adenovirus expressing mouse GM-CSF (Av1mGM). Mice were killed 1, 3, and 5 weeks after treatment to assess lungs for GM-CSF, surfactant protein B (SP-B), alveolar macrophage maturation, and type II cell proliferation. GM-CSF was detected in BAL fluid from GM-/- mice 1 week after Av1mGM treatment, and GM-CSF mRNA was detected by RT-PCR through 5 weeks. Five weeks after Av1mGM treatment, PAP was improved and SP-B decreased as assessed by ELISA and immunostaining. Increased numbers of alveolar macrophages stained with alpha-naphthyl acetate esterase (alpha-NAE) following treatment with Av1mGM. Local expression of GM-CSF with a recombinant adenovirus ameliorated PAP in the GM-/- mice in association with enhanced maturation of alveolar macrophages.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenoviridae / genetics*
  • Animals
  • Disease Models, Animal
  • Gene Expression / genetics
  • Genetic Therapy / methods
  • Genetic Vectors / genetics
  • Granulocyte-Macrophage Colony-Stimulating Factor / deficiency*
  • Granulocyte-Macrophage Colony-Stimulating Factor / genetics
  • Histocytochemistry
  • Lung / pathology*
  • Macrophages, Alveolar / enzymology
  • Mice
  • Mice, Knockout
  • Naphthols / metabolism
  • Proliferating Cell Nuclear Antigen / metabolism
  • Proteolipids / metabolism
  • Pulmonary Alveolar Proteinosis / genetics*
  • Pulmonary Alveolar Proteinosis / therapy
  • Pulmonary Surfactants / metabolism
  • Receptors, Antigen, T-Cell / antagonists & inhibitors
  • Receptors, Antigen, T-Cell / immunology

Substances

  • Naphthols
  • Proliferating Cell Nuclear Antigen
  • Proteolipids
  • Pulmonary Surfactants
  • Receptors, Antigen, T-Cell
  • alpha-naphthyl acetate
  • Granulocyte-Macrophage Colony-Stimulating Factor