Wüest T, Moosmayer D, Pfizenmaier K
Institute of Cell Biology and Immunology, University of Stuttgart, Allmandring 31, 70569 Stuttgart, Germany.
J Biotechnol. 2001 Dec 28;92(2):159-68. doi: 10.1016/s0168-1656(01)00355-8.
Bispecific antibodies directed against tumour associated antigens and the T cell receptor component CD3 for recruitment and tumour targeted activation of T cells represent a novel class of highly specific immunotherapeutics for cancer. We here describe the construction, eukaryotic expression and in vitro functional activity of a new T cell activating bispecific reagent, termed TTS for T cell targeting to the tumour stroma, comprised of a CD3 specific single chain antibody derivative (scFv) fused C-terminally to a 'fibroblast activation protein' (FAP) specific scFv that targets cytotoxic effector cells to FAP. FAP is highly expressed in the vascularised tumoural stroma of most lung, breast and colon carcinomas. It thus represents a selectively tumour associated, yet common marker of many solid tumours and is a potentially ideal candidate marker for efficient targeting of immune effector cells.
靶向肿瘤相关抗原和T细胞受体成分CD3以募集和肿瘤靶向激活T细胞的双特异性抗体代表了一类新型的高度特异性癌症免疫疗法。我们在此描述一种新型T细胞激活双特异性试剂的构建、真核表达及体外功能活性,该试剂称为TTS(用于T细胞靶向肿瘤基质),由一个C端融合了“成纤维细胞激活蛋白”(FAP)特异性单链抗体片段(scFv)的CD3特异性单链抗体衍生物组成,该FAP特异性scFv将细胞毒性效应细胞靶向FAP。FAP在大多数肺癌、乳腺癌和结肠癌的血管化肿瘤基质中高度表达。因此,它是一种选择性肿瘤相关的、但却是许多实体瘤的常见标志物,并且是有效靶向免疫效应细胞的潜在理想候选标志物。