Interleukin 35 and Hepatocyte Growth Factor; as a novel combined immune gene therapy for Multiple Sclerosis disease

Med Hypotheses. 2017 Nov:109:102-105. doi: 10.1016/j.mehy.2017.09.017. Epub 2017 Sep 22.

Abstract

An autoimmune demyelination disease of the Central Nervous System, Multiple Sclerosis, is a chronic inflammation which mostly involves young adults. Suffering people face functional loss with a severe pain. Most current MS treatments are focused on the immune response suppression. Approved drugs suppress the inflammatory process, but factually, there is no definite cure for Multiple Sclerosis. Recently developed knowledge has demonstrated that gene and cell therapy as a hopeful approach in tissue regeneration. The authors propose a novel combined immune gene therapy for Multiple Sclerosis treatment using anti-inflammatory and remyelination of Interleukine-35 and Hepatocyte Growth Factor properties, respectively. In this hypothesis Interleukine-35 and Hepatocyte Growth Factor introduce to Mesenchymal Stem Cells of EAE mouse model via an adenovirus based vector. It is expected that Interleukine-35 and Hepatocyte Growth Factor genes expressed from MSCs could effectively perform in immunotherapy of Multiple Sclerosis.

Keywords: CNS; Hepatocyte Growth Factor; Interleukine-35; Mesenchymal Stem Cells; Multiple Sclerosis.

MeSH terms

  • Adenoviridae / genetics
  • Animals
  • Anti-Inflammatory Agents / chemistry
  • Genetic Therapy*
  • Genetic Vectors
  • Hepatocyte Growth Factor / genetics*
  • Humans
  • Immune System
  • Inflammation
  • Interleukins / genetics*
  • Mice
  • Models, Biological
  • Multiple Sclerosis / genetics*
  • Multiple Sclerosis / therapy*
  • Regeneration
  • Signal Transduction
  • Stem Cells / cytology

Substances

  • Anti-Inflammatory Agents
  • HGF protein, human
  • Interleukins
  • interleukin-35, human
  • Hepatocyte Growth Factor