Modulation of autoimmune diseases by iPS cells

Methods Mol Biol. 2014:1213:365-77. doi: 10.1007/978-1-4939-1453-1_30.

Abstract

Autoimmune disease is typically caused by the activated self-reacted immune cells. The mainstream treatment to autoimmune disorders is composed of different mechanisms of immunosuppression. In recent years, a new subtype of T cells called regulatory T (Treg) cells have been identified to maintain the immune homeostasis in terms of suppressing the activated immune components. According to this discovery, it is suggested that treating autoimmune patients by supplementing Treg cells would be a good choice. However, due to their natural scarcity, it is difficult to isolate a desired number of Treg for this therapeutical approach. Here, we report that by using stem cells, especially the induced pluripotent stem (iPS) cells, we are able to generate a significant amount of Treg cells for the autoimmune prevention and treatment.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adoptive Transfer
  • Animals
  • Arthritis, Experimental
  • Autoimmune Diseases / immunology*
  • Autoimmune Diseases / metabolism*
  • Cell Differentiation
  • Cell Line
  • Disease Models, Animal
  • Flow Cytometry
  • Fluorescent Antibody Technique
  • Forkhead Transcription Factors / metabolism
  • Gene Expression
  • Genetic Vectors / genetics
  • Immune Tolerance
  • Immunohistochemistry
  • Immunomodulation*
  • Immunophenotyping
  • Induced Pluripotent Stem Cells / cytology
  • Induced Pluripotent Stem Cells / metabolism*
  • Male
  • Mice
  • Retroviridae / genetics
  • Transduction, Genetic

Substances

  • Forkhead Transcription Factors
  • Foxp3 protein, mouse