The Effect of Interferon-Beta Therapy on T-Helper 17/miR-326 and T-Helper 1/miR-29b-3p Axis in Relapsing-Remitting Multiple Sclerosis Patients

Neuroimmunomodulation. 2022;29(3):177-185. doi: 10.1159/000519777. Epub 2021 Nov 22.

Abstract

Background: We aimed to evaluate the therapeutic effects of interferon-beta (IFN-β) on hsa-miR29b-3p and hsa-miR326 in isolated T-helper (Th)1 and Th17 cells expressed by relapsing-remitting multiple sclerosis (RRMS) patients before and after 1 year of treatment with IFN-β.

Methods: The study was done on 19 RRMS patients pre- and posttreatment with IFN-β to evaluate the frequency of Th1 and Th17 cells by flow cytometry. The expression level of hsa-miR-29b-3p and hsa-miR-326 in isolated Th1 and Th17 cells was assessed by quantitative polymerase chain reaction. Enzyme-linked immunosorbent assay was also used to measure the plasma levels of I interferon -gamma and interleukin (IL)-17A.

Results: Th17 cells and plasma levels of IL-17A decreased in RRMS patients after IFN-β therapy but hsa-miR-29b-3p and hsa-miR-326 expression had no significant change in treated RRMS patients versus baseline. MxA gene expression was significantly induced upon IFN-β therapy in patients with RRMS.

Conclusion: IFN-β therapy is more effective on Th17 than Th1, but it does not reform altered expression of hsa-miR-326 and hsa-miR-29b-3p in Th17 and Th1, respectively.

Keywords: Hsa-miR-29b-3p; Hsa-miR-326; Interferon-beta; MxA.

MeSH terms

  • Humans
  • Interferon-beta* / therapeutic use
  • Interferon-gamma / blood
  • Interleukin-17 / blood
  • MicroRNAs* / genetics
  • Multiple Sclerosis* / drug therapy
  • Multiple Sclerosis, Relapsing-Remitting* / drug therapy
  • Th17 Cells / metabolism

Substances

  • IL17A protein, human
  • Interleukin-17
  • MIRN29a microRNA, human
  • MIRN326 microRNA, human
  • MicroRNAs
  • Interferon-beta
  • Interferon-gamma