From the bench to the bedside: ways to improve rituximab efficacy

被引:416
作者
Cartron, G
Watier, H
Golay, J
Solal-Celigny, P
机构
[1] CHRU, F-37044 Tours, France
[2] Univ Tours, UPRES EA, IPGA, Tours, France
[3] CHU, Lab Immunol, Tours, France
[4] Osped Riuniti Bergamo, France Lab Cellular & Gene Therapy G Lanzani, Bergamo, Italy
关键词
D O I
10.1182/blood-2004-03-1110
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Rituximab (MabThera, Rituxan) is a chimeric lgG1 monoclonal antibody that specifically targets the CD20 surface antigen expressed on normal and neoplastic B-lymphoid cells. Rituximab is currently used in the treatment of both follicular and aggressive B-cell non-Hodgkin lymphomas. Despite its demonstrated clinical effectiveness, its in vivo mechanisms of action remain unknown and could differ by subtype of lymphoma. Rituximab has been shown to induce apoptosis, complement-mediated lysis, and antibody-dependent cellular cytotoxicity in vitro, and some evidence points toward an involvement of these mechanisms in vivo. Rituximab also has a delayed therapeutic effect as well as a potential "vaccinal" effect. Here, we review the current understanding of the mechanism of action of rituximab and discuss approaches that could increase its clinical activity. A better understanding of how rituximab acts in vivo should maker it possible to develop new and more effective therapeutic strategies. (C) 2004 by The American Society of Hematology.
引用
收藏
页码:2635 / 2642
页数:8
相关论文
共 101 条
[1]  
Alas S, 2001, CANCER RES, V61, P5137
[2]  
Alas S, 2002, CLIN CANCER RES, V8, P836
[3]  
Alas S, 2001, CLIN CANCER RES, V7, P709
[4]   Targeted anti-cancer therapy using rituximab, a chimaeric anti-CD20 antibody (IDEC-C2B8) in the treatment of non-Hodgkin's B-cell lymphoma [J].
Anderson, DR ;
GrilloLopez, A ;
Varns, C ;
Chambers, KS ;
Hanna, N .
BIOCHEMICAL SOCIETY TRANSACTIONS, 1997, 25 (02) :705-708
[5]   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
[6]   Phase 1 study of interleukin-12 in combination with rituximab in patients with B-cell non-Hodgkin lymphoma [J].
Ansell, SM ;
Witzig, TE ;
Kurtin, PJ ;
Sloan, JA ;
Jelinek, DF ;
Howell, KG ;
Markovic, SN ;
Habermann, TM ;
Klee, GG ;
Atherton, PJ ;
Erlichman, C .
BLOOD, 2002, 99 (01) :67-74
[7]  
BAFFY G, 1993, J BIOL CHEM, V268, P6511
[8]   Complement-mediated cell death induced by rituximab in B-cell lymphoproliferative disorders is mediated in vitro by a caspase-independent mechanism involving the generation of reactive oxygen species [J].
Bellosillo, B ;
Villamor, N ;
López-Guillermo, A ;
Marcé, S ;
Esteve, J ;
Campo, E ;
Colomer, D ;
Montserrat, E .
BLOOD, 2001, 98 (09) :2771-2777
[9]   Association of serum Rituximab (IDEC-C2B8) concentration and anti-tumor response in the treatment of recurrent low-grade or follicular non-Hodgkin's lymphoma [J].
Berinstein, NL ;
Grillo-Lopez, AJ ;
White, CA ;
Bence-Bruckler, I ;
Maloney, D ;
Czuczman, M ;
Green, D ;
Rosenberg, J ;
McLaughlin, P ;
Shen, D .
ANNALS OF ONCOLOGY, 1998, 9 (09) :995-1001
[10]   Rituximab antiproliferative effect in B-lymphoma cells is associated with acid-sphingomyelinase activation in raft microdomains [J].
Bezombes, C ;
Grazide, S ;
Garret, C ;
Fabre, C ;
Quillet-Mary, A ;
Müller, S ;
Jaffrézou, JP ;
Laurent, G .
BLOOD, 2004, 104 (04) :1166-1173