Contribution of Th1 and Th2 cells to protection and pathology in experimental models of granulomatous lung disease

J Immunol. 2001 Mar 1;166(5):3432-9. doi: 10.4049/jimmunol.166.5.3432.

Abstract

Mice that had received adoptive transfer of DO11.10 TCR transgenic T cells polarized toward a Th1 or a Th2 phenotype were challenged with Ag-coated beads or with recombinant Mycobacterium tuberculosis expressing the OVA determinant. The resulting bead-induced pulmonary granulomas reflected the phenotype of the adoptively transferred T cells, with the Th2 cells promoting a fibrotic reaction. Mice receiving Th1 cells mounted an epitope-specific protective response to challenge with recombinant M. tuberculosis. Th2 recipients were characterized by enhanced weight loss and lung fibrosis during acute high-dose infection. The combination of TCR transgenic T cells and epitope-tagged mycobacteria provides a novel experimental model for investigation of the pathogenesis of tuberculosis.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adoptive Transfer
  • Animals
  • Antigens / administration & dosage
  • Antigens / immunology
  • Cells, Cultured
  • Cytokines / biosynthesis
  • Disease Models, Animal
  • Female
  • Granuloma, Respiratory Tract / etiology
  • Granuloma, Respiratory Tract / immunology*
  • Granuloma, Respiratory Tract / pathology*
  • Granuloma, Respiratory Tract / prevention & control
  • Injections, Intravenous
  • Lymphocyte Transfusion
  • Mice
  • Mice, Inbred BALB C
  • Mice, Transgenic
  • Microspheres
  • Mycobacterium tuberculosis / immunology
  • Ovalbumin / administration & dosage
  • Ovalbumin / immunology
  • Spleen / cytology
  • Spleen / immunology
  • Spleen / transplantation
  • Th1 Cells / immunology*
  • Th1 Cells / metabolism
  • Th1 Cells / transplantation
  • Th2 Cells / immunology*
  • Th2 Cells / metabolism
  • Th2 Cells / transplantation
  • Tuberculosis / etiology
  • Tuberculosis / immunology*
  • Tuberculosis / pathology*
  • Tuberculosis / prevention & control

Substances

  • Antigens
  • Cytokines
  • Ovalbumin