Genetically engineered Lactococcus lactis protect against house dust mite allergy in a BALB/c mouse model

PLoS One. 2014 Oct 7;9(10):e109461. doi: 10.1371/journal.pone.0109461. eCollection 2014.

Abstract

Background: Mucosal vaccine based on lactic acid bacteria is an attractive concept for the prevention and treatment of allergic diseases, but their mechanisms of action in vivo are poorly understood. Therefore, we sought to investigate how recombinant major dust mite allergen Der p2-expressing Lactococcus lactis as a mucosal vaccine induced the immune tolerance against house dust mite allergy in a mouse model.

Methods: Three strains of recombinant L. lactis producing Der p2 in different cell components (extracellular, intracellular and cell wall) were firstly constructed. Their prophylactic potential was evaluated in a Der p2-sensitised mouse model, and immunomodulation properties at the cellular level were determined by measuring cytokine production in vitro.

Results: Der p2 expressed in the different recombinant L. lactis strains was recognized by a polyclonal anti-Der p2 antibody. Oral treatment with the recombinant L. lactis prior sensitization significantly prevented the development of airway inflammation in the Der p2-sensitized mice, as determined by the attenuation of inflammatory cells infiltration in the lung tissues and decrease of Th2 cytokines IL-4 and IL-5 levels in bronchoalveolar lavage. In addition, the serum allergen-specific IgE levels were significantly reduced, and the levels of IL-4 in the spleen and mesenteric lymph nodes cell cultures were also markedly decreased upon allergen stimulation in the mice fed with the recombinant L. lactis strains. These protective effects correlated with a significant up-regulation of regulatory T cells in the mesenteric lymph nodes.

Conclusion: Oral pretreatment with live recombinant L. lactis prevented the development of allergen-induced airway inflammation primarily by the induction of specific mucosal immune tolerance.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Animals
  • Antibodies
  • Antigens, Dermatophagoides / biosynthesis
  • Antigens, Dermatophagoides / immunology*
  • Arthropod Proteins / biosynthesis
  • Arthropod Proteins / immunology*
  • Bronchoalveolar Lavage Fluid / chemistry
  • Bronchoalveolar Lavage Fluid / immunology
  • Cell Engineering / methods
  • Cell Wall / genetics
  • Cell Wall / metabolism
  • Cytosol / metabolism
  • Female
  • Immune Tolerance / drug effects
  • Immunity, Mucosal / drug effects*
  • Immunoglobulin E / biosynthesis
  • Immunomodulation
  • Interleukin-4 / antagonists & inhibitors
  • Interleukin-4 / biosynthesis
  • Interleukin-5 / antagonists & inhibitors
  • Interleukin-5 / biosynthesis
  • Lactococcus lactis / genetics
  • Lactococcus lactis / immunology*
  • Mice
  • Mice, Inbred BALB C
  • Probiotics / pharmacology*
  • Pyroglyphidae / chemistry
  • Pyroglyphidae / immunology
  • Respiratory Hypersensitivity / immunology
  • Respiratory Hypersensitivity / pathology
  • Respiratory Hypersensitivity / prevention & control*
  • T-Lymphocytes, Regulatory / cytology
  • T-Lymphocytes, Regulatory / drug effects
  • T-Lymphocytes, Regulatory / immunology
  • Vaccines / administration & dosage*
  • Vaccines / immunology

Substances

  • Antibodies
  • Antigens, Dermatophagoides
  • Arthropod Proteins
  • Dermatophagoides pteronyssinus antigen p 2
  • Interleukin-5
  • Vaccines
  • Interleukin-4
  • Immunoglobulin E

Grants and funding

This work was supported by the National Natural Science Foundation of China (No. 31200691), the National Science Fund for Distinguished Young Scholars (No. 31125021), the 111 project B07029, IRT124, and the Priority Academic Program Development of Jiangsu Higher Education Institutions. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.