Across rheumatic diseases

Systemic and local autoantibody responses to extracellular matrix proteins define inflammatory phenotypes across arthropathies

Rheumatology (Oxford)Published Cross-sectional study

Authors' conclusion

These findings demonstrate that autoantibodies against PRG4 and COMP are present across arthropathies with distinct patterns reflecting different pathogenic mechanisms.

Study context

Population
Healthy controls and patients with OA, RA or JIA
Exposure
OA, RA and JIA vs healthy controls
Outcome
Systemic and local (SF) levels of PRG4 and COMP and their autoantibodies
Methodological detailsELISA of serum and synovial fluid
  • ELISA of serum and synovial fluid

Main finding

As reported in the abstract

PRG4, COMP and their autoantibodies in serum and SF
  • Serum PRG4 significantly decreased in RA vs controls and OA; elevated in JIA
  • Serum cartilage oligomeric matrix protein (COMP) significantly elevated in OA and JIA vs controls and RA
  • SF PRG4 decreased in OA vs all other groups; SF COMP highest in OA and controls
  • Serum anti-PRG4 significantly elevated in all disease groups vs controls; RA and JIA also increased in SF
  • Anti-COMP significantly increased in RA and JIA serum and elevated in all disease groups in SF vs controls
  • Positive correlation between PRG4 protein and anti-PRG4 antibodies specifically in OA SF

Observational data: associations, not effects.

Original publication

Systemic and local autoantibody responses to extracellular matrix proteins define inflammatory phenotypes across arthropathies. Rheumatology (Oxford). Published 9 September 2026. doi:10.1093/rheumatology/keag487

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