Related Experiment Video
Updated: Mar 14, 2026

Murine Model of Allergen Induced Asthma
Published on: May 14, 2012
Bacterial extract (OM-85) with human-equivalent doses does not inhibit the development of asthma in a murine model
A Rodrigues1, L P Gualdi1, R G de Souza1
1Laboratory of Pediatric Respirology, Infant Center, Institute of Biomedical Research, Pontifícia Universidade Católica do Rio Grande do Sul, Porto Alegre, Brazil.
Background:
OM-85 is an immunostimulant bacterial lysate, which has been proven effective in reducing the number of lower airways infections. We investigated the efficacy of the bacterial lysate OM-85 in the primary prevention of a murine model of asthma.
Methods:
In the first phase of our study the animals received doses of 0.5μg, 5μg and 50μg of OM-85 through gavage for five days (days -10 to -6 of the protocol), 10 days prior to starting the sensitisation with ovalbumin (OVA), in order to evaluate the results of dose-response protocols. A single dose (5μg) was then chosen in order to verify in detail the effect of OM-85 on the pulmonary allergic response. Total/differential cells count and cytokine levels (IL-4, IL-5, IL-13 and IFN-γ) from bronchoalveolar lavage fluid (BALF), OVA-specific IgE levels from serum, lung function and lung histopathological analysis were evaluated.
Results:
OM-85 did not reduce pulmonary eosinophilic response, regardless of the dose used. In the phase protocol using 5μg/animal of OM-85, no difference was shown among the groups studied, including total cell and eosinophil counts in BALF, serum OVA-specific IgE, lung histopathologic findings and lung resistance. However, OM-85 decreased IL-5 and IL-13 levels in BALF.
Conclusions:
OM-85, administered in early life in mice in human-equivalent doses, does not inhibit the development of allergic pulmonary response in mice.
Insights
OM-85, an immunostimulant, did not prevent allergic lung responses in a mouse asthma model. While it reduced certain inflammatory markers, it did not inhibit the overall allergic pulmonary response.
Area of Science:
- Immunology
- Pulmonology
- Pharmacology
Background:
- OM-85 is an immunostimulant bacterial lysate known to reduce lower airway infections.
- Its efficacy in primary prevention of asthma in a murine model was investigated.
Purpose of the Study:
- To evaluate the efficacy of OM-85 in preventing the development of allergic pulmonary responses in a mouse model of asthma.
- To determine dose-response effects and specific impacts on allergic inflammation.
Main Methods:
- Mice received varying doses of OM-85 via gavage before ovalbumin sensitization.
- Evaluated bronchoalveolar lavage fluid (BALF) for cell counts and cytokines (IL-4, IL-5, IL-13, IFN-γ).
- Assessed serum OVA-specific IgE, lung function, and histopathology.
Main Results:
- OM-85 did not reduce pulmonary eosinophilic response or OVA-specific IgE levels.
- No significant differences were observed in total cell counts, lung function, or histopathology.
- A decrease in IL-5 and IL-13 levels in BALF was noted.
Conclusions:
- OM-85 administered in early life, at human-equivalent doses, did not inhibit the development of allergic pulmonary responses in mice.
- The study suggests OM-85 is not effective for primary prevention of asthma in this model.
More Related Videos
12:27The Utilization of Oropharyngeal Intratracheal PAMP Administration and Bronchoalveolar Lavage to Evaluate the Host Immune Response in Mice
Published on: April 2, 2014
14:48Visualizing Lung Cellular Adaptations during Combined Ozone and LPS Induced Murine Acute Lung Injury
Published on: March 21, 2021
Related Concept Videos
Asthma: Pathogenesis and Management
Asthma is classified as allergic and non-allergic. Allergens such as dust mites, pollen, and pet dander trigger allergic asthma, while factors like cold air, intense emotions, or exercise can induce non-allergic asthma.
Asthma-II: Pathophysiology and Classification
Additionally, environmental and genetic factors play crucial roles in determining an individual's susceptibility to asthma and the severity of their condition.
Critical processes in asthma pathophysiology include:
Asthma-I: Introduction