Orally administered heat-killed Lactobacillus paracasei MCC1849 enhances antigen-specific IgA secretion and induces follicular helper T cells in mice

PLoS One. 2018 Jun 13;13(6):e0199018. doi: 10.1371/journal.pone.0199018. eCollection 2018.

Abstract

Antigen-specific immunoglobulin (Ig) A plays a major role in host defense against infections in gut mucosal tissue. Follicular helper T (Tfh) cells are located in germinal centers and promote IgA production via interactions with germinal center B cells. Several studies have demonstrated that some lactic acid bacteria (LAB) strains activate the host's acquired immune system, inducing IgA secretion in the intestine. However, the precise molecular mechanisms underlying the effects of LAB on IgA production and Tfh cells are not fully resolved. Lactobacillus paracasei MCC1849 is a probiotic strain isolated from the intestine of a healthy adult. In this study, we investigated the effects of orally administered heat-killed MCC1849 on IgA production in the intestine and on Tfh cell induction in vivo. We found that orally administered MCC1849 induced antigen-specific IgA production in the small intestine, serum and lungs. We also observed that MCC1849 increased the proportion of IgA+ B cells and Tfh cells in Peyer's patches (PPs). In addition, MCC1849 increased the gene expression of IL-12p40, IL-10, IL-21, STAT4 and Bcl-6 associated with Tfh cell differentiation. These results suggest that orally administered MCC1849 enhances antigen-specific IgA production and likely affects Tfh cell differentiation in PPs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Animals
  • B-Lymphocytes / cytology
  • B-Lymphocytes / metabolism
  • Cell Differentiation
  • Cytokines / analysis
  • Cytokines / metabolism
  • Hot Temperature
  • Immunoglobulin A, Secretory / blood
  • Immunoglobulin A, Secretory / metabolism*
  • Influenza A Virus, H1N1 Subtype / pathogenicity
  • Intestine, Small / metabolism
  • Lacticaseibacillus paracasei / immunology*
  • Lung / metabolism
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Orthomyxoviridae Infections / prevention & control
  • Ovalbumin / immunology
  • Peyer's Patches / metabolism
  • Probiotics / administration & dosage
  • Proto-Oncogene Proteins c-bcl-6 / metabolism
  • T-Lymphocytes, Helper-Inducer / cytology
  • T-Lymphocytes, Helper-Inducer / immunology*
  • T-Lymphocytes, Helper-Inducer / metabolism

Substances

  • Cytokines
  • Immunoglobulin A, Secretory
  • Proto-Oncogene Proteins c-bcl-6
  • Ovalbumin

Grants and funding

This work was funded by Morinaga Milk Industry Co., Ltd. S Arai, N. Iwabuchi, S. Takahashi, J-Z Xiao and F. Abe are employees of Morinaga Milk Industry Co., Ltd. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.