Lactobacillus fermentum CJL-112 protects mice against influenza virus infection by activating T-helper 1 and eliciting a protective immune response

Int Immunopharmacol. 2014 Jan;18(1):50-4. doi: 10.1016/j.intimp.2013.10.020. Epub 2013 Nov 6.

Abstract

We have previously reported that nasally administered Lactobacillus fermentum CJL-112 (CJL-112) efficiently improves resistance against lethal influenza infection in both mice and chicken. The aim of the present study was to understand the underlying mechanisms of the significant anti-influenza activity of this lactobacilli strain. In vitro, co-culturing of the chicken macrophage cell line HD-11 with CJL-112 significantly increased nitric oxide (NO) production. In vivo, CJL-112 was nasally administered to BALB/c mice for 21 days prior to influenza A/NWS/33 (H1N1) virus (IFV) infection. Significant up-regulation of T-helper 1 (Th1) cytokines (IL-2, IFN-γ) was observed, while the levels of T-helper 2 (Th2) cytokines (IL-4, IL-5, IL-10) was either reduced or unchanged than that in control mice were. Furthermore, IgA and specific anti-influenza IgA levels increased significantly in the treated mice than those in untreated mice. Therefore, CJL-112 likely protects the mice against lethal IFV infection via stimulation of macrophages, activation of Th1 and augmentation of IgA production, when directly delivered into the respiratory tract.

Keywords: IgA; Influenza virus; Lactobacillus fermentum CJL-112; Nitric oxide production; Th1 immune response.

MeSH terms

  • Administration, Intranasal
  • Animals
  • Antibodies, Viral / metabolism
  • Cell Line
  • Chickens
  • Coinfection
  • Cytokines / metabolism
  • Female
  • Gram-Positive Bacterial Infections / immunology*
  • Immunity, Humoral
  • Influenza A Virus, H1N1 Subtype / immunology*
  • Limosilactobacillus fermentum / immunology*
  • Lymphocyte Activation
  • Mice
  • Mice, Inbred BALB C
  • Orthomyxoviridae Infections / immunology*
  • Th1 Cells / immunology*
  • Th1 Cells / microbiology
  • Th1 Cells / virology

Substances

  • Antibodies, Viral
  • Cytokines