Defects in B-lymphopoiesis and B-cell maturation underlie prolonged B-cell depletion in ANCA-associated vasculitis
Jazyk angličtina Země Spojené státy americké Médium electronic
Typ dokumentu časopisecké články
PubMed
38851295
PubMed Central
PMC11503191
DOI
10.1136/ard-2024-225587
PII: S0003-4967(24)66546-5
Knihovny.cz E-zdroje
- Klíčová slova
- B-lymphocytes, rituximab, vasculitis,
- MeSH
- ANCA-asociované vaskulitidy * imunologie farmakoterapie MeSH
- B-lymfocyty * imunologie MeSH
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- lymfocytární deplece metody MeSH
- lymfopoéza * MeSH
- receptor faktoru aktivujícího B-buňky * MeSH
- rituximab * terapeutické užití MeSH
- senioři MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- receptor faktoru aktivujícího B-buňky * MeSH
- rituximab * MeSH
OBJECTIVES: B-cell depletion time after rituximab (RTX) treatment is prolonged in antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) compared with other autoimmune diseases. We investigated central and peripheral B-cell development to identify the causes for the defect in B-cell reconstitution after RTX therapy. METHODS: We recruited 91 patients with AAV and performed deep phenotyping of the peripheral and bone marrow B-cell compartment by spectral flow and mass cytometry. B-cell development was studied by in vitro modelling and the role of BAFF receptor by quantitative PCR, western blot analysis and in vitro assays. RESULTS: Treatment-naïve patients with AAV showed low transitional B-cell numbers, suggesting impaired B-lymphopoiesis. We analysed bone marrow of treatment-naïve and RTX-treated patients with AAV and found reduced B-lymphoid precursors. In vitro modelling of B-lymphopoiesis from AAV haematopoietic stem cells showed intact, but slower and reduced immature B-cell development. In a subgroup of patients, after RTX treatment, the presence of transitional B cells did not translate in replenishment of naïve B cells, suggesting an impairment in peripheral B-cell maturation. We found low BAFF-receptor expression on B cells of RTX-treated patients with AAV, resulting in reduced survival in response to BAFF in vitro. CONCLUSIONS: Prolonged depletion of B cells in patients with AAV after RTX therapy indicates a B-cell defect that is unmasked by RTX treatment. Our data indicate that impaired bone marrow B-lymphopoiesis results in a delayed recovery of peripheral B cells that may be further aggravated by a survival defect of B cells. Our findings contribute to the understanding of AAV pathogenesis and may have clinical implications regarding RTX retreatment schedules and immunomonitoring after RTX therapy.
CIBSS Centre for Integrative Biological Signalling Studies University of Freiburg Freiburg Germany
Department of Orthopedics and Trauma Surgery University of Freiburg Freiburg im Breisgau Germany
Department of Paediatric Haematology and Oncology University Hospital Motol Prague Czech Republic
Division of Rheumatology and Clinical Immunology Medical University of Graz Graz Austria
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