Utilizing the BiTE (bispecific T-cell engager) platform for immunotherapy of cancer

被引:54
|
作者
Stieglmaier, Julia [1 ]
Benjamin, Jonathan [2 ]
Nagorsen, Dirk [3 ]
机构
[1] Amgen Res Munich, Global Clin Dev, Therapeut Area Oncol, D-81477 Munich, Germany
[2] Amgen Inc, Global Clin Dev, Therapeut Area Oncol, Thousand Oaks, CA 91320 USA
[3] Amgen Inc, Early Dev Oncol, Thousand Oaks, CA 91320 USA
关键词
bispecific antibody; BiTE (R); blinatumomab; cancer immunotherapy; T-cells; ACUTE LYMPHOBLASTIC-LEUKEMIA; BLINATUMOMAB; THERAPY;
D O I
10.1517/14712598.2015.1041373
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Various approaches of T-cell-based cancer immunotherapy are currently under investigation, among these are BiTE (bispecific T-cell engager) antibody constructs, which have a unique design and mechanism of action. They are constructed by genetically linking onto a single polypeptide chain the minimal binding domains of monoclonal antibodies for tumor-associated surface antigens and for the T-cell receptor-associated molecule CD3. Concurrent engagement of the target cell antigen and CD3 leads to activation of polyclonal cytotoxic T-cells, resulting in target cell lysis. Blinatumomab, a BiTE targeting CD19, is being investigated in a broad range of B-cell malignancies and has recently been approved in the USA by the US FDA for Philadelphia chromosome-negative relapsed/refractory B-acute lymphoblastic leukemia under the trade name BLINCYTO (TM). The BiTE platform is one of the clinically most advanced T-cell immunotherapy options.
引用
收藏
页码:1093 / 1099
页数:7
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