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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.
Abstract:
Autoantibodies targeting post-translational modified proteins represent key immunological hallmarks of Rheumatoid Arthritis (RA). In a previous study we demonstrated the presence of citrullinated and carbamylated proteins in extracellular microvesicles (EMVs) from plasma of RA patients. Since the pivotal role of TNFα in sustaining inflammatory and oxidative processes that promote protein modification, in this study we investigated the patterns of these post-translational modifications in EMVs isolated from RA patients before and after anti-TNFα treatment. Twelve consecutive RA patients, naïve to biological therapy, were enrolled and subjected to anti-TNFα therapy, which remained stable throughout the 8-month follow-up. EMVs, isolated from baseline (T0) and 8 months of follow-up (T8) plasma of RA patients, were measured by Nanoparticle Tracking Analysis or lysed and subjected to western blot analysis, using anti-citrulline or anti-carbamyl lysine antibodies. Anti-citrullinated and anti-carbamylated protein antibodies were also detected. Anti-TNFα treatment induced a significant reduction in the concentration of EMVs isolated from plasma of RA patients after 8 months of anti-TNFα treatment (P < 0.01). Moreover, in EMVs extracts citrullinated and carbamylated protein levels were significantly lower at T8, as compared to T0 (P < 0.01). Anti-TNFα treatment also induced a significant decrease of both anti-citrullinated and anti-carbamylated protein antibody levels, as well as of activity scores (SDAI and DAS28). These findings suggest the role of EMVs, as well as of citrullinated and carbamylated protein levels, as potential indicators of RA activity.
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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