Transplanted human umbilical cord mesenchymal stem cells facilitate lesion repair in B6.Fas mice

J Immunol Res. 2014:2014:530501. doi: 10.1155/2014/530501. Epub 2014 Dec 29.

Abstract

Background: Systemic lupus erythematosus (SLE) is a multisystem disease that is characterized by the appearance of serum autoantibodies. No effective treatment for SLE currently exists.

Methods: We used human umbilical cord mesenchymal stem cell (H-UC-MSC) transplantation to treat B6.Fas mice.

Results: After four rounds of cell transplantation, we observed a statistically significant decrease in the levels of mouse anti-nuclear, anti-histone, and anti-double-stranded DNA antibodies in transplanted mice compared with controls. The percentage of CD4(+)CD25(+)Foxp3(+) T cells in mouse peripheral blood significantly increased after H-UC-MSC transplantation.

Conclusions: The results showed that H-UC-MSCs could repair lesions in B6.Fas mice such that all of the relevant disease indicators in B6.Fas mice were restored to the levels observed in normal C57BL/6 mice.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Antinuclear / blood
  • CD4 Antigens / metabolism
  • DNA / immunology
  • Forkhead Transcription Factors / metabolism
  • Histones / immunology
  • Humans
  • Interleukin-2 Receptor alpha Subunit / metabolism
  • Lupus Erythematosus, Systemic / immunology
  • Lupus Erythematosus, Systemic / therapy*
  • Lymphocyte Count
  • Mesenchymal Stem Cell Transplantation*
  • Mesenchymal Stem Cells / physiology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Mutant Strains
  • T-Lymphocytes, Regulatory / immunology*
  • Transplantation, Heterologous
  • Umbilical Cord / cytology*

Substances

  • Antibodies, Antinuclear
  • CD4 Antigens
  • FOXP3 protein, human
  • Forkhead Transcription Factors
  • Histones
  • Interleukin-2 Receptor alpha Subunit
  • DNA