Reimagining antibody-dependent cellular cytotoxicity in cancer: the potential of natural killer cell engagers

被引:33
|
作者
Pinto, Sheena [1 ]
Pahl, Jens [1 ]
Schottelius, Arndt [1 ]
Carter, Paul J. [2 ]
Koch, Joachim [1 ]
机构
[1] Affimed GmbH, Heidelberg, Germany
[2] Genentech Inc, Dept Antibody Engn, San Francisco, CA USA
关键词
FC-GAMMA-RIIIA; NK CELLS; IN-VITRO; T-CELL; RECEPTOR; POLYMORPHISM; EXPANSION; EGFR; IGG; IMMUNITY;
D O I
10.1016/j.it.2022.09.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Bi-, tri- and multispecific antibodies have enabled the development of targeted cancer immunotherapies redirecting immune effector cells to eliminate malignantly transformed cells. These antibodies allow for simultaneous binding of surface antigens on malignant cells and activating receptors on innate immune cells, such as natural killer (NK) cells, macrophages, and neutrophils. Significant progress with such antibodies has been achieved, particularly in hematological malignancies. Nevertheless, severalmajor challenges remain, including increasing their immunotherapeutic efficacy in a greater proportion of patients, particularly in those harboring solid tumors, and overcoming dose-limiting toxicities and immunogenicity. Here, we discuss novel antibody-engineering developments designed to maximize the potential of NK cells by NK cell engagers mediating antibody-dependent cellular cytotoxicity (ADCC), thereby expanding the armamentarium for cancer immunotherapy.
引用
收藏
页码:932 / 946
页数:15
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