Class-switched B cells display response to therapeutic B-cell depletion in rheumatoid arthritis

被引:51
作者
Moeller, Burkhard [1 ]
Aeberli, Daniel [1 ]
Eggli, Stefan [2 ]
Fuhrer, Martin [1 ]
Vajtai, Istvan [3 ]
Voegelin, Esther [4 ]
Ziswiler, Hans-Rudolf [1 ]
Dahinden, Clemens A. [5 ]
Villiger, Peter M. [1 ]
机构
[1] Univ Hosp Bern, Inselspital, Clin Rheumatol Clin Immunol & Allergol, CH-3010 Bern, Switzerland
[2] Univ Hosp Bern, Inselspital, Dept Orthopaed Surg, CH-3010 Bern, Switzerland
[3] Univ Bern, Inst Pathol, Sect Neuropathol, CH-3010 Bern, Switzerland
[4] Univ Hosp Bern, Inselspital, Dept Orthopaed Plast & Reconstruct & Hand Surg, CH-3010 Bern, Switzerland
[5] Univ Hosp Bern, Inselspital, Inst Immunol, CH-3010 Bern, Switzerland
关键词
LYMPHOCYTE DEPLETION; AFFINITY MATURATION; ANTI-CD20; THERAPY; CLINICAL-RESPONSE; NECROSIS-FACTOR; DOUBLE-BLIND; RITUXIMAB; EFFICACY; MECHANISM; SAFETY;
D O I
10.1186/ar2686
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Introduction Reconstitution of peripheral blood (PB) B cells after therapeutic depletion with the chimeric anti-CD20 antibody rituximab (RTX) mimics lymphatic ontogeny. In this situation, the repletion kinetics and migratory properties of distinct developmental B-cell stages and their correlation to disease activity might facilitate our understanding of innate and adaptive B-cell functions in rheumatoid arthritis (RA). Methods Thirty-five 'RTX-naive' RA patients with active arthritis were treated after failure of tumour necrosis factor blockade in an open-label study with two infusions of 1,000 mg RTX. Prednisone dose was tapered according to clinical improvement from a median of 10 mg at baseline to 5 mg at 9 and 12 months. Conventional disease-modifying antirheumatic drugs were kept stable. Subsets of CD19+ B cells were assessed by flow cytometry according to their IgD and CD27 surface expression. Their absolute number and relative frequency in PB were followed every 3 months and were determined in parallel in synovial tissue (n = 3) or synovial fluid ( n = 3) in the case of florid arthritis. Results Six of 35 patients fulfilled the European League Against Rheumatism criteria for moderate clinical response, and 19 others for good clinical response. All PB B-cell fractions decreased significantly in number (P < 0.001) after the first infusion. Disease activity developed independently of the total B-cell number. B-cell repopulation was dominated in quantity by CD27(-)IgD(+) 'naive' B cells. The low number of CD27(+)IgD(-) class-switched memory B cells (MemB) in the blood, together with sustained reduction of rheumatoid factor serum concentrations, correlated with good clinical response. Class-switched MemB were found accumulated in flaring joints. Conclusions The present data support the hypothesis that control of adaptive immune processes involving germinal centre-derived, antigen, and T-cell-dependently matured B cells is essential for successful RTX treatment.
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页数:11
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