Vasculitis & polymyalgia rheumatica

Autoreactive Plasmablasts After B Cell Depletion With Rituximab and Relapses in Antineutrophil Cytoplasmic Antibody–Associated Vasculitis

Arthritis RheumatolPublished Mechanistic study

Authors' conclusion

The composition of the autoreactive B cell pool varies significantly following RTX treatment in AAV, and early plasmablast enrichment within the autoreactive pool is associated with future relapses.

Study context

Population
Patients with PR3-ANCA-positive ANCA-associated vasculitis (AAV) treated with rituximab (RTX) for remission induction and monitored after stopping therapy during long-term follow-up in a prospective clinical trial148 PBMC samples
Participants
23 patients
Comparison
Circulating PR3-specific B cell pool at B cell recurrence after RTX vs baseline; patients with relapse vs those in remission
Outcome
Autoreactive (PR3+) B cell pool at B cell recurrence (first sample with ≥10 B cells/μl after RTX)
Follow-up
B cell recurrence
Methodological detailsprospective, sequential flow cytometry
  • Prospective
  • Sequential flow cytometry

Main finding

As reported in the abstract

PR3+ B cell frequency among B cells higher than baseline
P < 0.01
Within PR3+ and total B cells, transitional and naive subsets higher and memory subsets lower than baseline
P < 0.001 for all comparisons
PR3+ plasmablast frequencies higher than baseline more likely in patients relapsing within the following 12 months vs sustained remission
P < 0.05

Original publication

Autoreactive Plasmablasts After B Cell Depletion With Rituximab and Relapses in Antineutrophil Cytoplasmic Antibody–Associated Vasculitis. Arthritis Rheumatol. Published 15 March 2023. doi:10.1002/art.42388

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