Thakur Archana, Lum Lawrence G
Barbara Ann Karmanos Cancer Institute, Wayne State University, Department of Medicine, Detroit, MI 48201, USA.
Curr Opin Mol Ther. 2010 Jun;12(3):340-9.
The binding of at least two molecular targets simultaneously with a single bispecific antibody is an attractive concept. The use of bispecific antibodies as possible therapeutic agents for cancer treatment was proposed in the mid-1980s. The design and production of bispecific antibodies using antibody- and/or receptor-based platform technology has improved significantly with advances in the knowledge of molecular manipulations, protein engineering techniques, and the expression of antigens and receptors on healthy and malignant cells. The common strategy for making bispecific antibodies involves combining the variable domains of the desired mAbs into a single bispecific structure. Many different formats of bispecific antibodies have been generated within the research field of bispecific immunotherapeutics, including the chemical heteroconjugation of two complete molecules or fragments of mAbs, quadromas, F(ab')2, diabodies, tandem diabodies and single-chain antibodies. This review describes key modifications in the development of bispecific antibodies that can improve their efficacy and stability, and provides a clinical perspective on the application of bispecific antibodies for the treatment of solid and liquid tumors, including the promises and research limitations of this approach.
用单个双特异性抗体同时结合至少两个分子靶点是一个很有吸引力的概念。20世纪80年代中期就有人提出将双特异性抗体用作癌症治疗的潜在治疗药物。随着分子操作知识、蛋白质工程技术以及健康细胞和恶性细胞上抗原与受体表达方面的进展,利用基于抗体和/或受体的平台技术设计和生产双特异性抗体有了显著改进。制备双特异性抗体的常见策略是将所需单克隆抗体的可变结构域组合成单一的双特异性结构。在双特异性免疫治疗研究领域已产生了许多不同形式的双特异性抗体,包括两个完整单克隆抗体分子或片段的化学异源缀合物、四聚体、F(ab')2、双抗体、串联双抗体和单链抗体。本文综述了双特异性抗体研发过程中能提高其疗效和稳定性的关键修饰,并提供了双特异性抗体用于治疗实体瘤和液体肿瘤的临床视角,包括这种方法的前景和研究局限性。