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释放T细胞的临床潜力:CD19/CD3双特异性T细胞衔接器(BiTE®)抗体构建体博纳吐单抗作为一种潜在疗法。

Unleashing the clinical power of T cells: CD19/CD3 bi-specific T cell engager (BiTE®) antibody construct blinatumomab as a potential therapy.

作者信息

Zimmerman Zachary, Maniar Tapan, Nagorsen Dirk

机构信息

Global Development, Amgen Inc., Thousand Oaks, CA 91320, USA

Global Development, Amgen Inc., Thousand Oaks, CA 91320, USA.

出版信息

Int Immunol. 2015 Jan;27(1):31-7. doi: 10.1093/intimm/dxu089. Epub 2014 Sep 19.

Abstract

Multi-agent chemotherapy is the standard treatment for most B cell malignancies. Since chemotherapy can be associated with significant toxicity and since relapses resistant to chemotherapy often develop, new therapies are needed. Blinatumomab (AMG 103 or MT103) is a late-stage candidate in clinical development, which belongs to a novel class of antibody constructs termed bi-specific T cell engager antibodies. This antibody construct has dual specificity for CD19 and CD3 and can re-direct polyclonal cytotoxic T lymphocytes toward the tumor. This review focuses on the pre-clinical and clinical development of blinatumomab as a powerful new tool in the treatment of B cell malignancies.

摘要

多药联合化疗是大多数B细胞恶性肿瘤的标准治疗方法。由于化疗可能会带来显著的毒性,且常常会出现对化疗耐药的复发情况,因此需要新的治疗方法。博纳吐单抗(AMG 103或MT103)是处于临床开发后期的候选药物,属于一类新型的抗体构建体,称为双特异性T细胞衔接抗体。这种抗体构建体对CD19和CD3具有双重特异性,能够将多克隆细胞毒性T淋巴细胞重定向至肿瘤细胞。本综述重点关注博纳吐单抗作为治疗B细胞恶性肿瘤的一种强大新工具的临床前和临床开发情况。

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