Early Increase of Circulating Transitional B Cells and Autoantibodies to Joint‐Related Proteins in Patients With Metastatic Melanoma Developing Checkpoint Inhibitor–Induced Inflammatory Arthritis

Arthritis RheumatolPublished Prospective cohort study

Authors' conclusion

Development of ICI-IA is accompanied by an increase in transitional B cells and by production of autoantibodies to joint-related proteins.

Study context

Population
Patients receiving immune checkpoint inhibitors (ICIs) to treat metastatic melanoma
Participants
7 vs 15
Exposure
ICI-induced inflammatory arthritis (IA) vs no immune-related adverse events after ICIs for metastatic melanoma
  • ICI-induced IA (ICI-IA)n = 7
  • non-IRAEn = 15reference
Outcome
Proportion of CD19+ B cells
Methodological detailsconsecutive recruitment, flow cytometry
  • Consecutive recruitment
  • Flow cytometry

Main finding

As reported in the abstract

P = 0.03

Observational data: associations, not effects.

Further findings

Absolute number of transitional B cells

P < 0.01

OutcomeOR (95% CI)P value
Higher transitional B cell levels and development of ICI-IA2.25 (1.03–4.9)P = 0.04
OutcomeICI-IAnon-IRAEP value
Proportion of transitional CD19+CD10+CD24high CD38high B cellsMedian8.1% (IQR 4.9–12.1%)3.6% (IQR 1.9–4.9%)P < 0.01
Autoantibodies to type II collagen epitopes43%0 eventsP = 0.02
  • Autoantibodies to type II collagen epitopes: detected in up to 43% of ICI-IA patients

Transitional B cells over time in ICI-IA

Increased before onset of overt ICI-IA and decreased between active and quiescent stages (P = 0.02)

Original publication

Early Increase of Circulating Transitional B Cells and Autoantibodies to Joint‐Related Proteins in Patients With Metastatic Melanoma Developing Checkpoint Inhibitor–Induced Inflammatory Arthritis. Arthritis Rheumatol. Published 14 March 2023. doi:10.1002/art.42406

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