Current status on B-cell depletion therapy in autoimmune diseases other than rheumatoid arthritis

被引:58
作者
Doerner, Thomas [1 ]
Isenberg, David [2 ]
Jayne, David [3 ]
Wiendl, Heinz [4 ]
Zillikens, Detlef [5 ]
Burmester, Gerd
机构
[1] Charite, Dept Med Rheumatol & Clin Immunol, D-10098 Berlin, Germany
[2] UCL, London WC1E 6BT, England
[3] Addenbrookes Hosp, Cambridge, England
[4] Univ Wurzburg, D-97070 Wurzburg, Germany
[5] Med Univ Lubeck, Lubeck, Germany
关键词
B cell; Therapy; Lupus; Multiple sclerosis; Pemphigus; SYSTEMIC-LUPUS-ERYTHEMATOSUS; EPIDERMOLYSIS-BULLOSA ACQUISITA; PRIMARY SJOGRENS-SYNDROME; REFRACTORY PEMPHIGUS-VULGARIS; MONOCLONAL-ANTIBODY RITUXIMAB; HUMANIZED ANTI-CD22 ANTIBODY; DEPENDENT NEPHROTIC SYNDROME; OPEN-LABEL; WEGENERS-GRANULOMATOSIS; LYMPHOCYTE DEPLETION;
D O I
10.1016/j.autrev.2009.08.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Since the approval of the chimeric anti-CD20 antibody rituximab for the treatment of adults with severe-to-moderate rheumatoid arthritis after an inadequate response to TNF blockade, B-cell depletion therapy has been used for the treatment of a broad range of refractory autoimmune disorders. Based on current experiences and a literature search, a systematic review and evaluation of the current status of B-cell depletion therapy in autoimmune diseases other than rheumatoid arthritis, including rheumatic, nephrologic, dermatologic and neurologic autoimmune entities, was performed by an international group of experts based at several academic centres. Although important questions remain about the value and place of B-cell depletion in autoimmune diseases other than RA, preliminary data indicate the value of this therapeutic approach in otherwise refractory patients. However, given the lack of robust data from large randomised controlled trials, anti-CD20 therapy should be considered on an individual basis in otherwise refractory patients and its use based on a risk/benefit net calculation. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:82 / 89
页数:8
相关论文
共 149 条
[1]   Successful treatment of refractory anterior scleritis in primary Sjogren's syndrome with rituximab [J].
Ahmadi-Simab, K ;
Lamprecht, P ;
Nölle, B ;
Ai, M ;
Gross, WL .
ANNALS OF THE RHEUMATIC DISEASES, 2005, 64 (07) :1087-1088
[2]   Treatment of pemphigus vulgaris with rituximab and intravenous immune globulin [J].
Ahmed, A. Razzaque ;
Spigelman, Zachary ;
Cavacini, Lisa A. ;
Posner, Marshall R. .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 355 (17) :1772-1779
[3]  
Anhalt G J, 1997, Adv Dermatol, V12, P77
[4]  
Anolik JH, 2007, BULL HOSP JT DIS, V65, P182
[5]   Rituximab improves peripheral B cell abnormalities in human systemic lupus erythematosus [J].
Anolik, JH ;
Barnard, J ;
Cappione, A ;
Pugh-Bernard, AE ;
Felgar, RE ;
Looney, RJ ;
Sanz, I .
ARTHRITIS AND RHEUMATISM, 2004, 50 (11) :3580-3590
[6]   The relationship of FcγRIIIa genotype to degree of B cell depletion by rituximab in the treatment of systemic lupus erythematosus [J].
Anolik, JH ;
Campbell, D ;
Felgar, RE ;
Young, F ;
Sanz, I ;
Rosenblatt, J ;
Looney, RJ .
ARTHRITIS AND RHEUMATISM, 2003, 48 (02) :455-459
[7]   Treatment of refractory pemphigus vulgaris with anti-CD20 monoclonal antibody (rituximab): Five cases [J].
Antonucci, Angela ;
Negosanti, Massimino ;
Tabanelli, Michela ;
Varotti, Claudio .
JOURNAL OF DERMATOLOGICAL TREATMENT, 2007, 18 (03) :178-183
[8]   Lack of efficacy of rituximab in Wegener's granulomatosis with refractory granulomatous manifestations [J].
Aries, P. M. ;
Hellmich, B. ;
Voswinkel, J. ;
Both, M. ;
Noelle, B. ;
Holl-Ulrich, K. ;
Lamprecht, P. ;
Gross, W. L. .
ANNALS OF THE RHEUMATIC DISEASES, 2006, 65 (07) :853-858
[9]   Anti-CD20 monoclonal antibody (rituximab) in the treatment of pemphigus [J].
Arin, MJ ;
Engert, A ;
Krieg, T ;
Hunzelmann, N .
BRITISH JOURNAL OF DERMATOLOGY, 2005, 153 (03) :620-625
[10]   SLE-associated transverse myelitis successfully treated with Rituximab (anti-CD20 monoclonal antibody) [J].
Armstrong, D. J. ;
McCarron, M. T. ;
Wright, G. D. .
RHEUMATOLOGY INTERNATIONAL, 2006, 26 (08) :771-772