Bispecific T-cell engagers: Towards understanding variables influencing the in vitro potency and tumor selectivity and their modulation to enhance their efficacy and safety

被引:147
作者
Ellerman, Diego [1 ]
机构
[1] Genentech Inc, Dept Prot Chem, San Francisco, CA 94080 USA
关键词
SINGLE-CHAIN ANTIBODY; MEDIATED LYSIS; MONOCLONAL-ANTIBODIES; NK CELLS; CYTOTOXIC LYMPHOCYTES; CHECKPOINT BLOCKADE; EFFECTOR FUNCTION; HODGKINS-DISEASE; ANTIGEN DENSITY; CYTOKINE STORM;
D O I
10.1016/j.ymeth.2018.10.026
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Bispecific molecules redirecting the cytotoxicity of T-cells are a growing class of therapeutics with numerous molecules being tested in clinical trials. However, it has been a long way since the proof of concept studies in the mid 1980's. In the process we have learnt about the impact of different variables related to the bispecific molecule and the target antigen on the potency of this type of drugs. This work reviews the insights gained and how that knowledge has been used to design more potent bispecific T-cell engagers. The more recent advancement of antibodies with this modality into safety studies in non-human primates and as well as in clinical studies has revealed potential toxicity liabilities for the mode of action. Modifications in existing antibody formats and new experimental molecules designed to mitigate these problems are discussed.
引用
收藏
页码:102 / 117
页数:16
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