Adipose tissue-derived mesenchymal stem cells increase skin allograft survival and inhibit Th-17 immune response

PLoS One. 2013 Oct 4;8(10):e76396. doi: 10.1371/journal.pone.0076396. eCollection 2013.

Abstract

Adipose tissue-derived mesenchymal stem cells (ADSC) exhibit immunosuppressive capabilities both in vitro and in vivo. Their use for therapy in the transplant field is attractive as they could render the use of immunosuppressive drugs unnecessary. The aim of this study was to investigate the effect of ADSC therapy on prolonging skin allograft survival. Animals that were treated with a single injection of donor allogeneic ADSC one day after transplantation showed an increase in donor skin graft survival by approximately one week. This improvement was associated with preserved histological morphology, an expansion of CD4(+) regulatory T cells (Treg) in draining lymph nodes, as well as heightened IL-10 expression and down-regulated IL-17 expression. In vitro, ADSC inhibit naïve CD4(+) T cell proliferation and constrain Th-1 and Th-17 polarization. In summary, infusion of ADSC one day post-transplantation dramatically increases skin allograft survival by inhibiting the Th-17 pathogenic immune response and enhancing the protective Treg immune response. Finally, these data suggest that ADSC therapy will open new opportunities for promoting drug-free allograft survival in clinical transplantation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue / cytology*
  • Animals
  • CD4-Positive T-Lymphocytes / cytology
  • CD4-Positive T-Lymphocytes / immunology
  • CD4-Positive T-Lymphocytes / metabolism
  • Cell Communication
  • Cell Differentiation
  • Cytokines / genetics
  • Cytokines / metabolism
  • Dendritic Cells / immunology
  • Dendritic Cells / metabolism
  • Graft Rejection / genetics
  • Graft Rejection / immunology
  • Graft Survival* / genetics
  • Graft Survival* / immunology
  • Immunophenotyping
  • Lymph Nodes / immunology
  • Lymph Nodes / metabolism
  • Mesenchymal Stem Cell Transplantation*
  • Mesenchymal Stem Cells / cytology*
  • Mesenchymal Stem Cells / metabolism*
  • Mice
  • Phenotype
  • Skin Transplantation*
  • Th17 Cells / immunology*
  • Transplantation, Homologous

Substances

  • Cytokines

Grants and funding

This study was supported by grants 07/07139-3, 06/55326-4, 10/52180-4 and 12/02270-2 from the State of Sao Paulo Foundation for Research Support (FAPESP), Brazilian Council of Scientific and Technologic Development (470533/2007-2, CNPq/DECIT/MS) and Complex Fluids INCT, Coordination of Improvement of Higher Education Personnel (CAPES Bex-2236/09-5). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.