Enhanced anti-B-cell tumor effects with anti-CD20 superantibody

被引:9
|
作者
Zhao, YF
Lou, DY
Burke, J
Kohler, H
机构
[1] Univ Kentucky, Lucille P Markey Canc Ctr, Dept Microbiol & Immunol, Lexington, KY 40536 USA
[2] Immpheron Inc, Lexington, KY USA
来源
JOURNAL OF IMMUNOTHERAPY | 2002年 / 25卷 / 01期
关键词
anti-CD20; antibody; apoptosis; tumor; immunotherapy;
D O I
10.1097/00002371-200201000-00006
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The data presented here describe a novel approach to enhance the use of antibodies in diagnostic and therapeutic applications, Using a peptide copied from a rare self-binding (autophilic) antibody structure, the authors were able to convert by chemical cross-linking an anti-CD20 antibody to a self-binding (autophilic) structure. The autophilic antibody exhibited better binding to target tumor cells than the naked antibody. By the mechanism of hyper-cross-linking a B-cell receptor (CD20) on tumor cells, the rate of apoptosis is significantly increased, leading to strong inhibition of tumor growth in culture. The demonstration of enhanced binding and apoptosis targeting the CD20 B-cell marker serves as an example for developing second-generation therapeutic antibodies against non-Hodgkin lymphoma.
引用
收藏
页码:57 / 62
页数:6
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