Treg cell resistance to apoptosis in DNA vaccination for experimental autoimmune encephalomyelitis treatment

PLoS One. 2012;7(11):e49994. doi: 10.1371/journal.pone.0049994. Epub 2012 Nov 14.

Abstract

Background: Regulatory T (Treg) cells can be induced with DNA vaccinations and protect mice from the development of experimental autoimmune encephalomyelitis (EAE), a mouse model of multiple sclerosis (MS). Tacrolimus (FK506) has been shown to have functions on inducing immunosuppression and augmenting apoptosis of pathologic T cells in autoimmune disease. Here we examined the therapeutic effect of DNA vaccine in conjunction with FK506 on EAE.

Methodology/principal findings: After EAE induction, C57BL/6 mice were treated with DNA vaccine in conjunction with FK506. Functional Treg cells were induced in treated EAE mice and suppressed Th1 and Th17 cell responses. Infiltrated CD4 T cells were reduced while Treg cells were induced in spinal cords of treated EAE mice. Remarkably, the activated CD4 T cells augmented apoptosis, but the induced Treg cells resisted apoptosis in treated EAE mice, resulting in alleviation of clinical EAE severity.

Conclusions/significance: DNA vaccine in conjunction with FK506 treatment ameliorates EAE by enhancing apoptosis of CD4 T cells and resisting apoptosis of induced Treg cells. Our findings implicate the potential of tolerogenic DNA vaccines for treating MS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Animals
  • Apoptosis / immunology*
  • Cytokines / metabolism
  • Encephalomyelitis, Autoimmune, Experimental / immunology*
  • Encephalomyelitis, Autoimmune, Experimental / prevention & control
  • Female
  • Flow Cytometry
  • Histological Techniques
  • Immune Tolerance / drug effects*
  • Mice
  • Mice, Inbred C57BL
  • Spinal Cord / immunology*
  • T-Lymphocyte Subsets / drug effects
  • T-Lymphocyte Subsets / immunology
  • T-Lymphocytes, Regulatory / immunology*
  • Tacrolimus / immunology
  • Tacrolimus / pharmacology*
  • Vaccines, DNA / immunology
  • Vaccines, DNA / pharmacology*

Substances

  • Cytokines
  • Vaccines, DNA
  • Tacrolimus

Grants and funding

This work was supported in part by National Natural Science Foundation of China (Project: 31270956) and the National Natural Science Foundation (Project: J1103520) for Undergraduates. The funding agencies had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.