Rituximab resistance

被引:188
作者
Rezvani, Andrew R. [1 ,2 ]
Maloney, David G. [1 ,2 ]
机构
[1] Fred Hutchinson Canc Res Ctr, Seattle, WA 98109 USA
[2] Univ Washington, Seattle, WA 98195 USA
基金
美国国家卫生研究院;
关键词
FC-GAMMA-RIIIA; NON-HODGKINS-LYMPHOMA; ANTI-CD20; MONOCLONAL-ANTIBODY; CHRONIC LYMPHOCYTIC-LEUKEMIA; STEM-CELL TRANSPLANTATION; FOLLICULAR LYMPHOMA; CD20; EXPRESSION; PHASE-I/II; IN-VIVO; RECEPTOR POLYMORPHISMS;
D O I
10.1016/j.beha.2011.02.009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Rituximab has become a ubiquitous component of treatment regimens for follicular non-Hodgkin lymphoma. Despite widespread clinical use, the mechanisms by which tumor cells resist rituximab-mediated destruction remain unclear. Rituximab relies in part on immune effector mechanisms for its antitumor effect, and thus resistance may be mediated not only by intrinsic tumor-cell alterations but also by the host immunological environment. In this article, we explore the mechanisms of action of rituximab, the incidence of rituximab resistance, and potential mechanisms of resistance. Finally, we discuss novel approaches to modulate the antibody, the tumor cell, and the host immunologic environment to overcome rituximab resistance. Further research into the mechanisms of rituximab resistance will be essential to improving the efficacy of anti-CD20 therapy in NHL and may also pay dividends in the optimization of monoclonal antibody therapy across a wide range of diseases. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:203 / 216
页数:14
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