Bacterial extract OM-85 BV protects mice against experimental chronic rhinosinusitis

Int J Clin Exp Pathol. 2015 Jun 1;8(6):6800-6. eCollection 2015.

Abstract

Objectives: To investigate the therapeutic effects of OM-85 BV as an adjunctive treatment on experimental chronic rhinosinusitis (CRS) in mice.

Methodology: Female BALB/c mice aged 8-12 weeks were sensitized and administrated by intranasal Aspergillus fumigatis (AF) three times per week for 1 week, 3 weeks, 2 months and 3 months (n = 10 each time point). The mice were randomly and equally assigned to four groups: normal control group, model group, OM-85-BV plus amoxicillin group, and isolated amoxicillin group. Inflammatory changes were determined by hematoxylin-eosin (HE) staining. The expression levels of suppressor of cytokine signaling (SOCS) 1, SOCS3, tumor necrosis factor (TNF)-α, and interferon (IFN)-γ in samples were assessed by using real-time PCR (RT-PCR) and Western blotting.

Results: There were significantly inflammatory and structural changes between the model and other groups. Compared to the model group, the mRNA expression levels of SOCS1, SOCS3, TNF-α, and IFN-γ were significantly decreased in OM-85-BV plus amoxicillin group and isolated amoxicillin group, along with the protein levels.

Conclusion: The bacterial extract OM-85 BV is a low-cost alternatively adjunctive drug to treat CRS with simple oral administration, good safety, and few side effects.

Keywords: IFN-γ; OM-85-BV; SOCS1; SOCS3; TNF-α.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adjuvants, Immunologic / administration & dosage
  • Adjuvants, Immunologic / pharmacology*
  • Administration, Oral
  • Amoxicillin / pharmacology
  • Animals
  • Antifungal Agents / pharmacology
  • Aspergillosis / drug therapy*
  • Aspergillosis / genetics
  • Aspergillosis / immunology
  • Aspergillosis / metabolism
  • Aspergillosis / microbiology
  • Aspergillus fumigatus / immunology
  • Aspergillus fumigatus / pathogenicity
  • Cell Extracts / administration & dosage
  • Cell Extracts / pharmacology*
  • Chronic Disease
  • Disease Models, Animal
  • Female
  • Inflammation Mediators / metabolism
  • Inhalation Exposure
  • Interferon-gamma / genetics
  • Interferon-gamma / metabolism
  • Mice, Inbred BALB C
  • RNA, Messenger / metabolism
  • Rhinitis / drug therapy*
  • Rhinitis / genetics
  • Rhinitis / immunology
  • Rhinitis / metabolism
  • Rhinitis / microbiology
  • Sinusitis / drug therapy*
  • Sinusitis / genetics
  • Sinusitis / immunology
  • Sinusitis / metabolism
  • Sinusitis / microbiology
  • Suppressor of Cytokine Signaling 1 Protein
  • Suppressor of Cytokine Signaling 3 Protein
  • Suppressor of Cytokine Signaling Proteins / genetics
  • Suppressor of Cytokine Signaling Proteins / metabolism
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Adjuvants, Immunologic
  • Antifungal Agents
  • Broncho-Vaxom
  • Cell Extracts
  • Inflammation Mediators
  • RNA, Messenger
  • Socs1 protein, mouse
  • Socs3 protein, mouse
  • Suppressor of Cytokine Signaling 1 Protein
  • Suppressor of Cytokine Signaling 3 Protein
  • Suppressor of Cytokine Signaling Proteins
  • Tumor Necrosis Factor-alpha
  • Amoxicillin
  • Interferon-gamma