Effects of diesel exhaust particle exposure on a murine model of asthma due to soybean

PLoS One. 2017 Jun 19;12(6):e0179569. doi: 10.1371/journal.pone.0179569. eCollection 2017.

Abstract

Background: Exposure to soybean allergens has been linked to asthma outbreaks. Exposure to diesel exhaust particles (DEP) has been associated with an increase in the risk of asthma and asthma exacerbation; however, in both cases the underlying mechanisms remain poorly understood, as does the possible interaction between the two entities.

Objective: To investigate how the combination of soybean allergens and DEP can affect the induction or exacerbation of asthma in a murine model.

Methods: BALB/c mice received intranasal instillations of saline, 3 or 5 mg protein/ml soybean hull extract (SHE), or a combination of one of these three solutions with DEP. Airway hyperresponsiveness (AHR), pulmonary inflammation in bronchoalveolar lavage, total serum immunoglobulin E and histological studies were assessed.

Results: A 5 mg protein/ml SHE solution was able by itself to enhance AHR (p = 0.0033), increase eosinophilic inflammation (p = 0.0003), increase levels of IL-4, IL-5, IL-13, IL-17A, IL-17F and CCL20, and reduce levels of IFN-γ. The combination of 5 mg protein/ml SHE with DEP also produced an increase in AHR and eosinophilic inflammation, but presented a slightly different cytokine profile with higher levels of Th17-related cytokines. However, while the 3 mg protein/ml SHE solution did not induce asthma, co-exposure with DEP resulted in a markedly enhanced AHR (p = 0.002) and eosinophilic inflammation (p = 0.004), with increased levels of IL-5, IL-17F and CCL20 and decreased levels of IFN-γ.

Conclusions & clinical relevance: The combination of soybean allergens and DEP is capable of triggering an asthmatic response through a Th17-related mechanism when the soybean allergen concentration is too low to promote a response by itself. DEP monitoring may be a useful addition to allergen monitoring in order to prevent new asthma outbreaks.

MeSH terms

  • Administration, Inhalation
  • Allergens / toxicity*
  • Animals
  • Area Under Curve
  • Asthma / etiology*
  • Asthma / pathology
  • Bronchoalveolar Lavage Fluid / chemistry
  • Bronchoalveolar Lavage Fluid / cytology
  • Chemokine CCL20 / blood
  • Cytokines / blood
  • Disease Models, Animal
  • Eosinophils / cytology
  • Eosinophils / immunology
  • Eosinophils / metabolism
  • Female
  • Glycine max / metabolism*
  • Immunoglobulin E / blood
  • Lung / physiology
  • Mice
  • Mice, Inbred BALB C
  • Particulate Matter / toxicity*
  • ROC Curve
  • Respiratory Hypersensitivity / etiology
  • Respiratory Hypersensitivity / pathology
  • Th17 Cells / immunology
  • Th17 Cells / metabolism
  • Vehicle Emissions / toxicity*

Substances

  • Allergens
  • Chemokine CCL20
  • Cytokines
  • Particulate Matter
  • Vehicle Emissions
  • Immunoglobulin E

Grants and funding

MJC is a researcher supported by the Miguel Servet program run by the Instituto de Salud Carlos III (CP12/03101). This project was supported by the Fundació Catalana de Pneumologia (FUCAP), Instituto de Salud Carlos III (CP12/03101) and European Regional Development Fund (FEDER). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.