Induction of remission by B lymphocyte depletion in eleven patients with refractory antineutrophil cytoplasmic antibody-associated vasculitis

被引:320
作者
Keogh, KA
Wylam, ME
Stone, JH
Specks, U
机构
[1] Mayo Clin, Rochester, MN USA
[2] Johns Hopkins Univ, Baltimore, MD USA
来源
ARTHRITIS AND RHEUMATISM | 2005年 / 52卷 / 01期
关键词
D O I
10.1002/art.20718
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. To assess the clinical effects of rituximab therapy in patients with antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV). Methods. The study group comprised 11 patients who had active AAV despite receiving maximally tolerated doses of cyclophosphamide or had contraindications for cyclophosphamide use. All patients had ANCA reactive against proteinase 3. The patients received rituximab infusions and glucocorticoids to induce remission. Three patients also received plasma exchange. No other immunosuppressive agents were used. Glucocorticoids were tapered as soon as control of disease activity was achieved. Disease activity was monitored using the Birmingham Vasculitis Activity Score, modified for Wegener's granulomatosis. Results. Rituximab therapy was well tolerated by all patients, and adverse events were rare. Following the rituximab infusions, circulating B lymphocytes became undetectable, and ANCA titers decreased significantly. Remission was achieved in all patients and was maintained while B lymphocytes were absent. Conclusion. The ability to achieve stable remissions with rituximab in patients with AAV refractory to conventional therapy suggests that B lymphocyte depletion may be a safe, effective, mechanism-based treatment modality for treatment of patients with these conditions.
引用
收藏
页码:262 / 268
页数:7
相关论文
共 19 条
  • [1] Boomsma MM, 2000, ARTHRITIS RHEUM-US, V43, P2025, DOI 10.1002/1529-0131(200009)43:9<2025::AID-ANR13>3.0.CO
  • [2] 2-O
  • [3] CUPPS TR, 1982, J IMMUNOL, V128, P2453
  • [4] Eriksson P., 2003, Kidney & Blood Pressure Research, V26, P294
  • [5] Goodnow CC, 2001, LANCET, V357, P2115
  • [6] Pathophysiology of ANCA-associated vasculitides: are ANCA really pathogenic?
    Heeringa, P
    Tervaert, JWC
    [J]. KIDNEY INTERNATIONAL, 2004, 65 (05) : 1564 - 1567
  • [7] WEGENER GRANULOMATOSIS - AN ANALYSIS OF 158 PATIENTS
    HOFFMAN, GS
    KERR, GS
    LEAVITT, RY
    HALLAHAN, CW
    LEBOVICS, RS
    TRAVIS, WD
    ROTTEM, M
    FAUCI, AS
    [J]. ANNALS OF INTERNAL MEDICINE, 1992, 116 (06) : 488 - 498
  • [8] A randomized trial of maintenance therapy for vasculitis associated with antineutrophil cytoplasmic autoantibodies
    Jayne, D
    Rasmussen, N
    Andrassy, K
    Bacon, P
    Tervaert, JWC
    Dadoniene, J
    Ekstrand, A
    Gaskin, G
    Gregorini, G
    de Groot, K
    Gross, W
    Hagen, EC
    Mirapeix, E
    Pettersson, E
    Siegert, C
    Sinico, A
    Tesar, V
    Westman, K
    Pusey, C
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2003, 349 (01) : 36 - 44
  • [9] Jayne D. R. W., 2003, Kidney & Blood Pressure Research, V26, P294
  • [10] Memory B cells specific for the NC16A domain of the 180 kDa bullous pemphigoid autoantigen can be detected in peripheral blood of bullous pemphigoid patients and induced in vitro to synthesize autoantibodies
    Leyendeckers, H
    Tasanen, K
    Bruckner-Tuderman, L
    Zillikens, D
    Sitaru, C
    Schmitz, J
    Hunzelmann, N
    [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2003, 120 (03) : 372 - 378