Rituximab: A promising therapy in systemic lupus erythernatosus

被引:68
作者
Thatayatikom, A [1 ]
White, AJ [1 ]
机构
[1] Washington Univ, Sch Med,St Louis Childrens Hosp, Div Immunol Rheumatol, Dept Pediat, St Louis, MO 63110 USA
关键词
systemic lupus erythematosus; CD20; B cell depletion; rituximab;
D O I
10.1016/j.autrev.2005.05.006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Several trials of new immunologic agents in systemic lupus erythematosus (SLE) have recently been undertaken. Rituximab, a chimeric antibody directed against CD20 on B lymphocytes, has emerged as a promising therapy. Based upon preliminary data, clinical efficacy of rituximab has been documented in both pediatric and adult-onset SLE patients. The specific manifestations reported to be beneficially affected include lupus nephritis, arthralgia/arthritis, serositis, cutaneous vasculitis, mucositis, rashes, fatigue and neurologic symptoms. Although rituximab's mechanisms of action are incompletely understood, the effects of rituximab are likely mediated by antibody-dependent cell-mediated cytotoxicity and the induction of apoptosis. The resultant repopulation of B cells, alteration of abnormal B cell homeostasis and down-regulation of costimulatory molecules on both B and T cells all likely contribute to clinical efficacy. Good tolerability of rituximab is reported with rare serious side effects. The positive response to rituximab verifies a central role for B cells in SLE. This article highlights the clinical experience of rituximab therapy in both pediatric and adult-onset SLE. These data suggest a promising role for rituximab in the treatment of SLE. Further controlled trials and long-term outcome studies are imperative to further define its clinical application and to improve the care of patients. (C) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:18 / 24
页数:7
相关论文
共 20 条
[1]   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
[2]   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
[3]   Therapeutic activity of humanized anti-CD20 monoclonal antibody and polymorphism in IgG Fc receptor FcγRIIIa gene [J].
Cartron, G ;
Dacheux, L ;
Salles, G ;
Solal-Celigny, P ;
Bardos, P ;
Colombat, P ;
Watier, H .
BLOOD, 2002, 99 (03) :754-758
[4]   Rituximab in childhood systemic lupus erythematosus refractory to conventional immunosuppression - Case report [J].
Edelbauer, M ;
Jungraithmayr, T ;
Zimmerhackl, LB .
PEDIATRIC NEPHROLOGY, 2005, 20 (06) :811-813
[5]   Efficacy of B-cell-targeted therapy with rituximab in patients with rheumatoid arthritis [J].
Edwards, JCW ;
Szczepanski, L ;
Szechinski, J ;
Filipowicz-Sosnowska, A ;
Emery, P ;
Close, DR ;
Stevens, RM ;
Shaw, T .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (25) :2572-2581
[6]   Remission of refractory lupus nephritis with a protocol including rituximab [J].
Fra, GP ;
Avanzi, GC ;
Bartoli, E .
LUPUS, 2003, 12 (10) :783-787
[7]   T cells in the pathogenesis of systemic lupus erythematosus [J].
Hoffman, RW .
CLINICAL IMMUNOLOGY, 2004, 113 (01) :4-13
[8]   Effective B cell depletion with rituximab in the treatment of autoimmune diseases [J].
Kneitz, C ;
Wilhelm, M ;
Tony, HP .
IMMUNOBIOLOGY, 2002, 206 (05) :519-527
[9]   An open study of B lymphocyte depletion in systemic lupus erythematosus [J].
Leandro, MJ ;
Edwards, JC ;
Cambridge, G ;
Ehrenstein, MR ;
Isenberg, DA .
ARTHRITIS AND RHEUMATISM, 2002, 46 (10) :2673-2677
[10]   Systemic lupus erythematosus: an autoimmune disease of B cell hyperactivity [J].
Lipsky, PE .
NATURE IMMUNOLOGY, 2001, 2 (09) :764-766