Interleukin-12 suppresses filaria-induced pulmonary eosinophilia, deposition of major basic protein and airway hyperresponsiveness

Parasite Immunol. 1998 Oct;20(10):455-62. doi: 10.1046/j.1365-3024.1998.00174.x.

Abstract

Tropical Pulmonary Eosinophilia (TPE) is a severe form of allergic asthma caused by the host inflammatory response to filarial helminths in the lung microvasculature, and is characterized by pulmonary eosinophilia, increased filarial-specific IgG and IgE antibodies, and airway hyperresponsiveness. The current study examined the effect of IL-12 on pulmonary eosinophilia, deposition of eosinophil major basic protein and airway hyperresponsiveness in mice inoculated i.v. with Brugia malayi microfilariae. Injection of recombinant murine IL-12 modulated the T helper (Th) response in the lungs from Th2- to Th1-like, with elevated IFN-gamma, and decreased IL-4 and IL-5 production. Consistent with this shift in cytokine response, antigen-specific IgG2a was elevated, and IgG1 and total serum IgE were decreased. In addition, eosinophils in BAL fluid from IL-12 treated mice were reduced from 56% to 11%, and there was no detectable MBP on respiratory epithelial cells. Importantly, IL-12 suppressed airway hyperresponsiveness compared with saline-injected control animals. Taken together, these data clearly demonstrate that by modulating Th associated cytokine production, IL-12 down-regulates filaria-induced lung immunopathology.

Publication types

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

MeSH terms

  • Animals
  • Antibodies, Helminth / blood
  • Antigens, Helminth / immunology
  • Bronchial Hyperreactivity / immunology*
  • Brugia malayi / immunology
  • Chick Embryo
  • Cytokines / analysis
  • Enzyme-Linked Immunosorbent Assay
  • Eosinophilia / immunology*
  • Female
  • Filariasis / immunology*
  • Gerbillinae
  • Immunoglobulin E / blood
  • Immunoglobulin G / blood
  • Interleukin-12 / administration & dosage
  • Interleukin-12 / pharmacology*
  • Lung / drug effects*
  • Lung / immunology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Microfilariae / immunology
  • Recombinant Proteins / administration & dosage
  • Recombinant Proteins / immunology
  • Recombinant Proteins / pharmacology
  • Spleen / immunology

Substances

  • Antibodies, Helminth
  • Antigens, Helminth
  • Cytokines
  • Immunoglobulin G
  • Recombinant Proteins
  • Interleukin-12
  • Immunoglobulin E