Post-translational modifications in extracellular microvesicles from plasma of rheumatoid arthritis patients

S Recalchi1,2, G Riitano1, F Ucci3

  • 1Department of Experimental Medicine, 'Sapienza' University of Rome, Rome, Italy.

Insights

Anti-tumor necrosis factor-alpha (TNFα) therapy reduced extracellular microvesicles (EMVs) and protein modifications in Rheumatoid Arthritis (RA) patients. These changes correlate with decreased RA activity, suggesting EMVs and modified proteins as potential RA biomarkers.

Area of Science:

  • Immunology
  • Rheumatology
  • Biochemistry

Background:

  • Autoantibodies targeting post-translationally modified proteins are hallmarks of Rheumatoid Arthritis (RA).
  • Extracellular microvesicles (EMVs) in RA patients contain citrullinated and carbamylated proteins.
  • Tumor necrosis factor-alpha (TNFα) drives inflammatory and oxidative processes that promote protein modification.

Purpose of the Study:

  • To investigate the impact of anti-TNFα therapy on post-translational modifications in EMVs from RA patients.
  • To assess changes in EMVs and autoantibody levels before and after anti-TNFα treatment.

Main Methods:

  • Twelve RA patients, treatment-naïve, received stable anti-TNFα therapy for 8 months.
  • EMVs were isolated from plasma at baseline (T0) and 8 months (T8).
  • EMV concentration was measured by Nanoparticle Tracking Analysis; protein modifications (citrullination, carbamylation) were assessed by Western blot. Autoantibodies were also measured.

Main Results:

  • Anti-TNFα treatment significantly reduced EMV concentration (p<0.01).
  • Levels of citrullinated and carbamylated proteins within EMVs were significantly lower at T8 compared to T0 (p<0.01).
  • Anti-TNFα therapy also decreased anti-citrullinated and anti-carbamylated antibody levels and RA activity scores (SDAI, DAS28).

Conclusions:

  • EMVs and their modified protein content may serve as potential indicators of RA disease activity.
  • Anti-TNFα therapy impacts EMV-associated protein modifications, correlating with clinical improvement in RA patients.

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