Stem cell based delivery of IFN-beta reduces relapses in experimental autoimmune encephalomyelitis

J Neuroimmunol. 2008 May 30;196(1-2):67-81. doi: 10.1016/j.jneuroim.2008.02.014. Epub 2008 May 8.

Abstract

Interferon-beta (IFN-beta), an approved treatment of multiple sclerosis (MS), produces only partial clinical responses. IFN-beta therapy has been limited by its short serum half-life and limited ability to cross the blood brain barrier. We have developed a means of delivering the IFN-beta gene both systemically and into the central nervous system (CNS) using bone marrow stem cells (BMSCs) as a vehicle and examined the therapeutic efficacy of this approach in experimental autoimmune encephalomyelitis (EAE), an animal model of MS. A retroviral expression vector (pLXSN-IFNbeta) was used to stably transfect virus producer PA317 cells to generate retrovirus containing the IFN-beta gene which then was used to transduce BMSCs. IFN-beta engineered BMSCs were transplanted (i.v.) into mice that then were immunized with proteolipoprotein (PLP) to initiate EAE. IFN-beta-engineered BMSCs transplanted mice showed a significant inhibition of EAE onset, and the overall clinical severity was less compared to control groups. IFN-beta delivery strongly reduced infiltration of mononuclear cells possibly by inhibiting cell adhesion molecules. Reduced demyelination and increased remyelination were also observed in the IFN-beta treated group. Furthermore, inhibition of the pro-inflammatory cytokines TNF-alpha, IFN-gamma and IL-12 and enhanced expression of the anti-inflammatory cytokines IL-10, IL-4 and TGF-beta was observed in CNS tissue. In addition, mice receiving IFN-beta had reduced apoptosis and increases in growth promoting factors including BDNF, CNTF, PDGF and VEGF. These results suggest that BMSCs can be used as vehicles to deliver the IFN-beta into the CNS. This is a potentially novel therapeutic approach which might be used in MS and other diseases of the CNS in which drug access is limited.

Publication types

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

MeSH terms

  • Animals
  • Antigens, CD34 / metabolism
  • Bone Marrow Cells / metabolism
  • Bone Marrow Cells / physiology*
  • Bone Marrow Transplantation / methods*
  • Caspase 3 / genetics
  • Caspase 3 / metabolism
  • Cells, Cultured
  • Cytokines / genetics
  • Cytokines / metabolism
  • Disease Models, Animal
  • Encephalomyelitis, Autoimmune, Experimental / chemically induced
  • Encephalomyelitis, Autoimmune, Experimental / prevention & control*
  • Enzyme-Linked Immunosorbent Assay / methods
  • Female
  • Gene Transfer Techniques
  • In Situ Nick-End Labeling
  • Intercellular Adhesion Molecule-1 / genetics
  • Intercellular Adhesion Molecule-1 / metabolism
  • Intercellular Signaling Peptides and Proteins / genetics
  • Intercellular Signaling Peptides and Proteins / metabolism
  • Interferon-beta / biosynthesis
  • Interferon-beta / genetics
  • Interferon-beta / therapeutic use*
  • Mice
  • Myelin Basic Protein / genetics
  • Myelin Basic Protein / metabolism
  • Myelin Proteolipid Protein
  • Peptide Fragments
  • Secondary Prevention
  • Vascular Cell Adhesion Molecule-1 / genetics
  • Vascular Cell Adhesion Molecule-1 / metabolism

Substances

  • Antigens, CD34
  • Cytokines
  • Icam1 protein, mouse
  • Intercellular Signaling Peptides and Proteins
  • Myelin Basic Protein
  • Myelin Proteolipid Protein
  • Peptide Fragments
  • Vascular Cell Adhesion Molecule-1
  • myelin proteolipid protein (139-151)
  • Intercellular Adhesion Molecule-1
  • Interferon-beta
  • Caspase 3