Impact of Rituximab on Immunoglobulin Concentrations and B Cell Numbers after Cyclophosphamide Treatment in Patients with ANCA-Associated Vasculitides

被引:118
作者
Venhoff, Nils [1 ]
Effelsberg, Nora M. [1 ]
Salzer, Ulrich [1 ,2 ]
Warnatz, Klaus [1 ,2 ]
Peter, Hans Hartmut [1 ,2 ]
Lebrecht, Dirk [1 ]
Schlesier, Michael [1 ,2 ]
Voll, Reinhard E. [1 ,2 ]
Thiel, Jens [1 ,2 ]
机构
[1] Univ Hosp Freiburg, Dept Rheumatol & Clin Immunol, Freiburg, Germany
[2] Univ Hosp Freiburg, Ctr Chron Immunodeficiency CCI, Freiburg, Germany
来源
PLOS ONE | 2012年 / 7卷 / 05期
关键词
ANTIBODY-ASSOCIATED VASCULITIS; RHEUMATOLOGY; 1990; CRITERIA; CHURG-STRAUSS-SYNDROME; WEGENERS-GRANULOMATOSIS; STAPHYLOCOCCUS-AUREUS; LYMPHOCYTE DEPLETION; ARTHRITIS; CLASSIFICATION; DISEASE; IMMUNODEFICIENCY;
D O I
10.1371/journal.pone.0037626
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Objective: To assess the impact of immunosuppressive therapy with cyclophosphamide (CYC) and rituximab (RTX) on serum immunoglobulin (Ig) concentrations and B lymphocyte counts in patients with ANCA-associated vasculitides (AAVs). Methods: Retrospective analysis of Ig concentrations and peripheral B cell counts in 55 AAV patients. Results: CYC treatment resulted in a decrease in Ig levels (median; interquartile range IQR) from IgG 12.8 g/L (8.15-15.45) to 9.17 g/L (8.04-9.90) (p = 0.002), IgM 1.05 g/L (0.70-1.41) to 0.83 g/L (0.60-1.17) (p = 0.046) and IgA 2.58 g/L (1.71-3.48) to 1.58 g/L (1-31-2.39) (p = 0.056) at a median follow-up time of 4 months. IgG remained significantly below the initial value at 14.5 months and 30 months analyses. Subsequent RTX treatment in patients that had previously received CYC resulted in a further decline in Ig levels from pre RTX IgG 9.84 g/L (8.71-11.60) to 7.11 g/L (5.75-8.77; p = 0.007), from pre RTX IgM 0.84 g/L (0.63-1.18) to 0.35 g/L (0.23-0.48; p<0.001) and from pre RTX IgA 2.03 g/L (1.37-2.50) to IgA 1.62 g/L (IQR 0.84-2.43; p = 0.365) 14 months after RTX. Treatment with RTX induced a complete depletion of B cells in all patients. After a median observation time of 20 months median B lymphocyte counts remained severely suppressed (4 B-cells/mu l, 1.25-9.5, p<0.001). Seven patients (21%) that had been treated with CYC followed by RTX were started on Ig replacement because of severe bronchopulmonary infections and serum IgG concentrations below 5 g/L. Conclusions: In patients with AAVs, treatment with CYC leads to a decline in immunoglobulin concentrations. A subsequent RTX therapy aggravates the decline in serum immunoglobulin concentrations and results in a profoundly delayed B cell repopulation. Surveying patients with AAVs post CYC and RTX treatment for serum immunoglobulin concentrations and persisting hypogammaglobulinemia is warranted.
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