Design and Production of Bispecific Antibodies

被引:175
|
作者
Wang, Qiong [1 ]
Chen, Yiqun [1 ]
Park, Jaeyoung [1 ]
Liu, Xiao [1 ]
Hu, Yifeng [1 ]
Wang, Tiexin [1 ]
McFarland, Kevin [1 ]
Betenbaugh, Michael J. [1 ]
机构
[1] Johns Hopkins Univ, Dept Chem & Biomol Engn, Baltimore, MD 21218 USA
基金
美国国家科学基金会;
关键词
single-chain variable fragment (scFv); bispecific antibody; quadroma technology; knobs-into-holes; CrossMAb; bispecific T-cell engager (BiTE); SINGLE-CHAIN-FV; SCFV ANTIBODY; V-H; PERIPLASMIC EXPRESSION; VARIABLE FRAGMENT; PROTEIN STABILITY; PHAGE DISPLAY; HIGH-AFFINITY; ESCHERICHIA-COLI; DOMAIN INTERFACE;
D O I
10.3390/antib8030043
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
With the current biotherapeutic market dominated by antibody molecules, bispecific antibodies represent a key component of the next-generation of antibody therapy. Bispecific antibodies can target two different antigens at the same time, such as simultaneously binding tumor cell receptors and recruiting cytotoxic immune cells. Structural diversity has been fast-growing in the bispecific antibody field, creating a plethora of novel bispecific antibody scaffolds, which provide great functional variety. Two common formats of bispecific antibodies on the market are the single-chain variable fragment (scFv)-based (no Fc fragment) antibody and the full-length IgG-like asymmetric antibody. Unlike the conventional monoclonal antibodies, great production challenges with respect to the quantity, quality, and stability of bispecific antibodies have hampered their wider clinical application and acceptance. In this review, we focus on these two major bispecific types and describe recent advances in the design, production, and quality of these molecules, which will enable this important class of biologics to reach their therapeutic potential.
引用
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页数:30
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