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IL-17 and related cytokines involved in the pathology and immunotherapy of multiple sclerosis: Current and future developments

Cytokine Growth Factor Rev. 2014 Aug;25(4):403-13. doi: 10.1016/j.cytogfr.2014.07.013. Epub 2014 Jul 29.

Abstract

Multiple sclerosis (MS), an autoimmune neurological disorder, is driven by self-reactive T helper (Th) cells. Research on the role of Th17 lymphocytes in MS pathogenesis has made significant progress in identifying various immunological as well as environmental factors that induce the differentiation and expansion of these cells, different subsets of Th17 cells with varying degrees of pathogenicity, and the role of the secreted effector cytokines. While approved therapies for MS offer significant benefit to patients, there remain unmet needs. Ongoing clinical trials aim to translate the advanced knowledge of Th17 cytokines to improved therapies. This review discusses the current status and future developments of research into the role of Th17 and related cytokines in MS pathogenesis and therapy.

Keywords: Cytokines; EAE; Multiple sclerosis; Th17; Therapy.

Publication types

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

MeSH terms

  • Animals
  • Autoimmunity / immunology
  • Cell Differentiation / immunology
  • Central Nervous System / immunology
  • Central Nervous System / pathology
  • Encephalomyelitis, Autoimmune, Experimental / immunology*
  • Encephalomyelitis, Autoimmune, Experimental / pathology
  • Humans
  • Immunotherapy / methods*
  • Inflammation Mediators / immunology
  • Interferon-beta / therapeutic use
  • Interleukin-17 / immunology
  • Interleukin-17 / therapeutic use*
  • Mice
  • Multiple Sclerosis / immunology*
  • Multiple Sclerosis / pathology
  • Th17 Cells / cytology
  • Th17 Cells / immunology*

Substances

  • IL17A protein, human
  • Inflammation Mediators
  • Interleukin-17
  • Interferon-beta