Fcγ receptors in Norwegian multiple sclerosis patients and healthy controls

S Gavasso1, Ø Torkildsen, T H Marøy

  • 1Department of Clinical Medicine, University of Bergen, Bergen, Norway.

Abstract

Insights

Treatments for relapsing-remitting multiple sclerosis (RRMS) like interferon-beta (INF-β) or glatiramer acetate (GA) may not significantly alter Fc gamma receptors (FcγR) on immune cells. FcγR2b gene variations also do not appear to increase MS risk.

Area of Science:

  • Immunology
  • Neuroimmunology
  • Pharmacology

Background:

  • Multiple sclerosis (MS) is an immune-mediated central nervous system disorder.
  • Fc gamma receptors (FcγR) play a role in autoimmune diseases.

Purpose of the Study:

  • To investigate the impact of interferon-beta (INF-β) and glatiramer acetate (GA) on Fcγ receptor expression and mRNA levels in multiple sclerosis (MS) patients.
  • To analyze FcγR2b polymorphisms in MS patients and healthy controls.

Main Methods:

  • Studied 16 Norwegian relapsing-remitting MS (RRMS) patients undergoing INF-β or GA treatment.
  • Assessed FcγR1a, FcγR2a, FcγR3b positive cells and FcγR mRNA levels in leukocytes.
  • Analyzed FcγR2b polymorphisms in 127 RRMS patients and 54 healthy controls.

Main Results:

  • INF-β or GA treatment increased FcγR positive lymphocytes but had minimal long-term effect on FcγR expression or mRNA levels in leukocytes.
  • No significant differences in FcγR2b genotype or allele frequencies were found between RRMS patients and healthy controls.

Conclusions:

  • INF-β or GA treatment likely does not significantly regulate FcγRs on immune cells in RRMS.
  • FcγR2b polymorphisms do not appear to influence susceptibility to MS.

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