Translational Medicine in Action: Anti-CD20 Therapy in Lymphoma

被引:34
|
作者
Lim, Sean H. [1 ]
Levy, Ronald [1 ]
机构
[1] Stanford Univ, Dept Med, Div Oncol, Stanford, CA 94305 USA
来源
JOURNAL OF IMMUNOLOGY | 2014年 / 193卷 / 04期
关键词
B-CELL LYMPHOMA; CHRONIC LYMPHOCYTIC-LEUKEMIA; CHEMOTHERAPY PLUS RITUXIMAB; MONOCLONAL ANTIIDIOTYPE ANTIBODY; CHOP-LIKE CHEMOTHERAPY; NON-HODGKINS-LYMPHOMA; CD20; ANTIBODY; SIGNIFICANTLY INCREASES; YOUNG-PATIENTS; IN-VIVO;
D O I
10.4049/jimmunol.1490027
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The introduction of rituximab for B cell lymphoma in the late 1990s inaugurated a new era of cancer therapy showcasing mAbs. mAbs are in principle an amalgamation of two characteristics of a perfect anticancer drug. First, rituximab is a therapy targeted to the tumor cell, but it carries fewer side effects than does chemotherapy. Second, with its ability to directly engage the host immune system, it could potentially elicit longer lasting anticancer immunity, although this remains to be proven. This review highlights the fundamental scientific discoveries that allowed the development of clinically successful anti-CD20mAbs. Since the approval of rituximab, a considerable amount of work has been undertaken by different groups trying to understand the workings and limitations of anti-CD20s. All of these efforts will be critical in designing new mAbs to CD20 and other targets and, ultimately, of anticancer mAbs that will improve on, or even replace, chemotherapy.
引用
收藏
页码:1519 / 1524
页数:6
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