Effect of glatiramer acetate (Copaxone) on the immunophenotypic and cytokine profile and BDNF production in multiple sclerosis: a longitudinal study

Neurosci Lett. 2006 Oct 9;406(3):270-5. doi: 10.1016/j.neulet.2006.07.043. Epub 2006 Aug 24.

Abstract

We assessed the effect of glatiramer acetate (GA) on the immunophenotypic and cytokine profile and the BDNF production by peripheral blood mononuclear cells, and their association with the clinical response in 19 naïve-treated MS patients prospectively followed-up after GA therapy. Two patients withdrew the therapy. After a median follow-up of 21 months, twelve were considered responders and five as non-responders. Non-responder patients had significant longer disease duration and a higher EDSS score at baseline. In the responder group, a significant decrease in the percentage of INF-gamma producing total lymphocytes, CD4+ and CD8+ T cells, and reduced percentage of IL-2 producing CD4+ and CD8+ T cells were observed at 12, 18 and 24 months. These changes were associated with a significant increase in the percentage of CD3+, CD4+ and CD4(+) CD45RA(+) T cells, and BDNF production from month 6 that remained significant throughout the study. We did not observe significant changes in the nonresponder group for any of the parameters studied. Our data suggest that GA treatment induces a downmodulation of proinflammatory cytokines associated with the regulation of the peripheral T cell compartment and with increased production of BDNF that might be related to the clinical response.

Publication types

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

MeSH terms

  • Adjuvants, Immunologic / pharmacology*
  • Adjuvants, Immunologic / therapeutic use
  • Adult
  • Brain-Derived Neurotrophic Factor / metabolism*
  • Cytokines / metabolism*
  • Female
  • Flow Cytometry / methods
  • Glatiramer Acetate
  • Humans
  • Longitudinal Studies
  • Lymphocyte Activation / drug effects
  • Male
  • Middle Aged
  • Multiple Sclerosis / drug therapy
  • Multiple Sclerosis / immunology*
  • Multiple Sclerosis / metabolism*
  • Peptides / pharmacology*
  • Peptides / therapeutic use
  • T-Lymphocyte Subsets / drug effects
  • Time Factors

Substances

  • Adjuvants, Immunologic
  • Brain-Derived Neurotrophic Factor
  • Cytokines
  • Peptides
  • Glatiramer Acetate