Therapeutic potential of umbilical cord blood cells for type 1 diabetes mellitus

J Diabetes. 2015 Nov;7(6):762-73. doi: 10.1111/1753-0407.12286. Epub 2015 Jun 29.

Abstract

Type 1 diabetes mellitus (T1DM) is a chronic disorder that results from autoimmune-mediated destruction of pancreatic islet β-cells. However, to date, no conventional intervention has successfully treated the disease. The optimal therapeutic method for T1DM should effectively control the autoimmunity, restore immune homeostasis, preserve residual β-cells, reverse β-cell destruction, and protect the regenerated insulin-producing cells against re-attack. Umbilical cord blood is rich in regulatory T (T(reg)) cells and multiple types of stem cells that exhibit immunomodulating potential and hold promise in their ability to restore peripheral tolerance towards pancreatic islet β-cells through remodeling of immune responses and suppression of autoreactive T cells. Recently, reinfusion of autologous umbilical cord blood or immune cells from cord blood has been proposed as a novel therapy for T1DM, with the advantages of no risk to the donors, minimal ethical concerns, a low incidence of graft-versus-host disease and easy accessibility. In this review, we revisit the role of autologous umbilical cord blood or immune cells from cord blood-based applications for the treatment of T1DM.

Keywords: immune cells; regulatory T cell; stem cell; type 1 diabetes mellitus; umbilical cord blood; 关键词:免疫细胞,调节性T细胞,干细胞,1型糖尿病,脐血.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Autoimmunity
  • Cord Blood Stem Cell Transplantation*
  • Diabetes Mellitus, Type 1 / blood
  • Diabetes Mellitus, Type 1 / diagnosis
  • Diabetes Mellitus, Type 1 / immunology
  • Diabetes Mellitus, Type 1 / surgery*
  • Humans
  • Insulin-Secreting Cells* / immunology
  • Insulin-Secreting Cells* / metabolism
  • Insulin-Secreting Cells* / pathology
  • T-Lymphocytes, Regulatory / immunology
  • Transplantation, Autologous
  • Treatment Outcome