Rheumatoid arthritis

Anticitrullinated peptide antibody epitope expansion and the HLA DRB1 ‘shared epitope’ are less common in seropositive checkpoint inhibitor-induced inflammatory arthritis than in longstanding rheumatoid arthritis

RMD OpenPublished Cross-sectional study

Authors' conclusion

Patients with ICI-IA had lower ACPA titres and targeted fewer ACPA epitopes than longstanding patients with RA, and there were no significant differences in the presence of the shared epitope between those that developed ICI-IA and ICI controls.

Study context

Population
Patients with CCP+ ICI-IA and patients with rheumatoid arthritis (RA) (early and longstanding disease)
Exposure
CCP+ ICI-IA vs CCP+ RA (early and longstanding); ICI-IA vs immune checkpoint inhibitors (ICI) controls for HLA DRB1 shared epitope
Outcome
Degree of anticitrullinated peptide antibodies (ACPA) epitope expansion (IgG ACPA reactivities to 18 putative RA-associated citrullinated proteins)
Methodological detailsbead-based antigen array, HLA DRB1 typing
  • Bead-based antigen array
  • HLA DRB1 typing

Main finding

As reported in the abstract

ACPA levels and number of distinct ACPA epitopes
  • ICI-IA vs RA: P < 0.001

Observational data: associations, not effects.

Further findings

OutcomeP value
Clinical characteristics, CCP+ ICI-IA vs CCP+ RAICI-IA vs RA · olderP < 0.001
Clinical characteristics, CCP+ ICI-IA vs CCP+ RAICI-IA vs RA · less likely to have positive RFP < 0.001
Clinical characteristics, CCP+ ICI-IA vs CCP+ RAICI-IA vs RA · shorter duration of symptomsP < 0.001

Frequency of HLA DRB1 shared epitope

No differences between ICI-IA and ICI controls

Original publication

Anticitrullinated peptide antibody epitope expansion and the HLA DRB1 ‘shared epitope’ are less common in seropositive checkpoint inhibitor-induced inflammatory arthritis than in longstanding rheumatoid arthritis. RMD Open. Published 23 June 2023. doi:10.1136/rmdopen-2023-003012

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