MicroRNA 26a Expression in Peripheral Blood Mononuclear Cells and Correlation with Serum Interleukin-17 in

Fatma M Mahmoud1, Nadia M ElSheshtawy1, Wafaa K Zaki1

  • 1Department of Medical Microbiology & Immunology, Faculty of Medicine, Ain-Shams University, Cairo, Egypt.

Insights

This study found increased levels of microRNA 26a (miR26a) and Interleukin 17 (IL17) in patients with relapsing-remitting multiple sclerosis (MS). These biomarkers may play a role in MS pathogenesis.

Area of Science:

  • Neuroimmunology
  • Molecular Biology

Background:

  • Multiple sclerosis (MS) is a chronic inflammatory demyelinating disease.
  • T helper 17 (Th17) cells are key players in MS pathogenesis.
  • MicroRNAs are increasingly recognized for their role in Th17 cell differentiation and potential therapeutic applications.

Purpose of the Study:

  • To investigate microRNA 26a (miR26a) expression in peripheral blood mononuclear cells of relapsing-remitting MS patients.
  • To compare miR26a levels with healthy controls.
  • To examine the association between miR26a levels and serum Interleukin 17 (IL17) in MS patients.

Main Methods:

  • Quantitative polymerase chain reaction (qPCR) was used to measure miR26a expression.
  • Enzyme-linked immunosorbent assay (ELISA) was employed to determine serum IL17 levels.
  • Forty relapsing-remitting MS patients and twenty healthy controls were included in the study.

Main Results:

  • A significant upregulation of miR26a and IL17 was observed in total MS patients and those in the remitting phase compared to controls (P < 0.001).
  • The relapsing MS group showed a significant increase in miR26a expression (P= 0.004) but not IL17 levels.
  • No significant correlation was found between miR26a expression and serum IL17 levels in MS patients (r= 0.08, P= 0.62).

Conclusions:

  • Both miR26a and IL17 are significantly elevated in relapsing-remitting MS patients.
  • These findings suggest that miR26a and IL17 are important biomarkers in the pathogenesis and development of MS.

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