Multiple challenges in a mouse model of chemical-induced asthma lead to tolerance: ventilatory and inflammatory responses are blunted, immunologic humoral responses are not

Toxicology. 2009 Mar 29;257(3):144-52. doi: 10.1016/j.tox.2008.12.020. Epub 2008 Dec 30.

Abstract

To improve our mouse model of chemical-induced asthma we compared a single with a multiple intranasal challenge protocol. BALB/c mice received toluene diisocyanate (TDI) or vehicle on each ear (days 1 and 8) with the first challenge by intranasal instillation given on day 15. In a "long" protocol, the mice received 1 to 6 intranasal instillations, with 1-week interval. In a "short" protocol, the mice received 6 intranasal challenges over a period of 10 days. The "early" ventilatory response and methacholine reactivity were measured. Broncho-alveolar-lavage (BAL), total serum immunoglobulins and draining lymph nodes were analyzed. After 1, 2 or 3 TDI challenges, a significant increase in airway reactivity, total cell count and neutrophils (15-20%) was found in TDI-treated mice. This response diminished with increasing numbers of challenges in both models. The percentage CD4(+) and CD8(+) cells decreased and the percentage CD19(+) cells increased in the lymph nodes, but these returned to control values with multiple challenges. IL-4 secretion increased in cervical lymph node cells in vitro. Total serum IgE levels were persistently increased in TDI-treated mice. Although humoral signs of allergy remain increased after multiple challenges, diminishing ventilatory and inflammatory responses are indicative of the induction of tolerance.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Intranasal
  • Animals
  • Antibody Formation / drug effects*
  • Asthma / chemically induced*
  • Asthma / immunology*
  • Bronchial Hyperreactivity / chemically induced
  • Bronchial Hyperreactivity / pathology
  • Bronchoalveolar Lavage Fluid / cytology
  • Bronchoconstrictor Agents
  • Cytokines / biosynthesis
  • Immune Tolerance / drug effects*
  • Immunoglobulin E / biosynthesis
  • Immunoglobulin G / biosynthesis
  • Inflammation / pathology*
  • Lung / pathology
  • Lymph Nodes / cytology
  • Lymph Nodes / drug effects
  • Lymphocytes / drug effects
  • Lymphocytes / metabolism
  • Male
  • Methacholine Chloride
  • Mice
  • Mice, Inbred BALB C
  • Respiratory Mechanics / drug effects*

Substances

  • Bronchoconstrictor Agents
  • Cytokines
  • Immunoglobulin G
  • Methacholine Chloride
  • Immunoglobulin E