Probiotics increase T regulatory cells and reduce severity of experimental colitis in mice

World J Gastroenterol. 2013 Feb 7;19(5):742-9. doi: 10.3748/wjg.v19.i5.742.

Abstract

Aim: To investigate the effect of probiotics on regulating T regulatory cells and reducing the severity of experimental colitis in mice.

Methods: Forty C57/BL mice were randomly divided into four groups. Colitis was induced in the mice using 2,4,6-trinitrobenzene sulfonic acid (TNBS). After 10-d treatment with Bifico capsules (combined bifidobacterium, lactobacillus and enterococcus), body weight, colonic weight, colonic weight index, length of colon, and histological scores were evaluated. CD4+CD25+Foxp3+T cell in mesenteric lymph nodes were measured by flow cytometry, and cytokines in colonic tissue homogenates were analyzed by a cytometric bead array.

Results: The colonic weight index and the colonic weight of colitis mice treated with Bifico were lower than that of TNBS-induced mice without treatment. However, colonic length and percent of body weight amplification were higher than in TNBS-induced mice without treatment. Compared with TNBS-induced mice without treatment, the level of CD4+CD25+Foxp3+T cells in mesenteric lymph nodes, the expression of interleukin (IL)-2, IL-4 and IL-10 in colonic tissues from colitis mice treated with Bifico were upregulated, and tumor necrosis factor-α and interferon-γ were downregulated.

Conclusion: Probiotics effectively treat experimental colitis by increasing CD4+CD25+Foxp3+T cell and regulating the balance of Th1 and Th2 cytokines in the colonic mucosa.

Keywords: CD4CD25T cell; Cytokine; Probiotics; Ulcerative colitis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomarkers / metabolism
  • CD4 Lymphocyte Count
  • Colitis / chemically induced
  • Colitis / immunology
  • Colitis / microbiology
  • Colitis / pathology
  • Colitis / therapy*
  • Colon / immunology*
  • Colon / microbiology*
  • Colon / pathology
  • Cytokines / metabolism
  • Disease Models, Animal
  • Forkhead Transcription Factors / metabolism
  • Inflammation Mediators / metabolism
  • Interleukin-2 Receptor alpha Subunit / metabolism
  • Intestinal Mucosa / immunology*
  • Intestinal Mucosa / microbiology
  • Intestinal Mucosa / pathology
  • Mice
  • Mice, Inbred C57BL
  • Probiotics*
  • Severity of Illness Index
  • T-Lymphocytes, Regulatory / immunology*
  • Trinitrobenzenesulfonic Acid
  • Up-Regulation

Substances

  • Biomarkers
  • Cytokines
  • Forkhead Transcription Factors
  • Foxp3 protein, mouse
  • Il2ra protein, mouse
  • Inflammation Mediators
  • Interleukin-2 Receptor alpha Subunit
  • Trinitrobenzenesulfonic Acid