INFβ treatment affects global DNA methylation in monocytes of patients with multiple sclerosis

Susana Nogueira Diniz1, Claudia Forlin da Silva2, Inara Tais de Almeida3

  • 1Universidade Anhanguera de São Paulo, UNIAN, Programa de Pós-Graduação em Farmácia e Biotecnologia e Inovação em Saúde, Rua Raimundo Pereira de Magalhães, 3305, Pirituba, Zip Code: 05145-200 São Paulo, SP, Brazil.

Insights

Global DNA methylation patterns differ between immune cells in multiple sclerosis (MS). Monocyte DNA methylation was notably impacted by interferon-beta (IFNβ) treatment in patients with MS.

Area of Science:

  • Immunology
  • Epigenetics
  • Neuroscience

Background:

  • Complex diseases arise from interactions between genetic and epigenetic factors.
  • Altered DNA methylation patterns are linked to inflammation and disease activity in multiple sclerosis (MS).
  • Understanding cell-type-specific epigenetic modifications is crucial for disease insights.

Purpose of the Study:

  • To investigate differences in global DNA methylation between lymphocytes and monocytes in MS patients versus healthy controls.
  • To explore the impact of interferon-beta (IFNβ) treatment on DNA methylation in MS patients.

Main Methods:

  • Peripheral blood mononuclear cells (PBMCs) were isolated from 33 patients with relapsing-remitting MS (PwRMS) and 5 healthy controls.
  • DNA was extracted using the phenol-chloroform method.
  • Global DNA methylation levels were quantified using the Imprint® Methylated DNA Quantification Kit.

Main Results:

  • A cell-type-specific pattern of global DNA methylation was observed.
  • Monocyte global DNA methylation levels were significantly altered in patients with MS.
  • IFNβ treatment demonstrated a significant effect on monocyte global DNA methylation.

Conclusions:

  • Global DNA methylation exhibits cell-type specificity in the context of MS.
  • Monocytes represent a key cell type where epigenetic alterations, particularly global DNA methylation, are influenced by MS and its treatment.
  • These findings highlight the role of epigenetics in MS pathogenesis and therapeutic response.