Gene therapy-mediated modulation of immune processes in the central nervous system

Roberto Furlan, Stefano Pluchino, Gianvito Martino

Research output: Contribution to journalArticlepeer-review

Abstract

Selective interference with immune processes in the central nervous system (CNS) is a very difficult task because of the limitations associated with the delivery of immuno modulatory molecules across the blood brain barrier. Systemic administration of immune-mediators, either by conventional routes or by intramuscularly or intravenous gene therapy, is hampered by severe side effects and alters immune-system functions also in peripheral organs. To overcome these problems, different gene therapy strategies have been developed to deliver immuno modulatory molecules directly within the central nervous system. The use of engineered CNS antigen-specific circulating cells as selective delivery vehicles, the direct injection of gene vectors into the brain parenchyma, or also the ependymal route, have been proposed as possible alternative gene therapy protocols to selectively interfere with immuno-pathological processes in the CNS. We will review the use of these CNS-targeted gene therapy protocols for the treatment of experimental autoimmune encephalomyelitis (EAE), the prototypical experimental immune-mediated disease of the CNS, and therefore discuss the relevance of these results for the therapy of multiple sclerosis (MS) the most common, immune-mediated, demyelinating disease of the CNS in humans.

Original languageEnglish
Pages (from-to)2002-2008
Number of pages7
JournalCurrent Pharmaceutical Design
Volume9
Issue number24
DOIs
Publication statusPublished - 2003

Keywords

  • And growth factors
  • Central nervous system
  • Cytokines
  • Experimental autoimmune encephalomyelitis
  • Gene therapy
  • Multiple sclerosis

ASJC Scopus subject areas

  • Molecular Medicine
  • Pharmacology, Toxicology and Pharmaceutics(all)

Fingerprint Dive into the research topics of 'Gene therapy-mediated modulation of immune processes in the central nervous system'. Together they form a unique fingerprint.

Cite this