Weidle Ulrich H, Georges Guy, Tiefenthaler Georg
Roche Pharma Research and Early Development (pRED), Roche Innovation Center Penzberg, Roche Diagnostics GmbH, Penzberg, Germany.
Cancer Genomics Proteomics. 2014 Nov-Dec;11(6):267-77.
Tumor-related antigens can be presented as peptides forming complexes with major histocompatibility complex (MHC) molecules that interact with T-cell receptors, thus generating an immunologic anti-tumor response. Unfortunately, however, this response can be decreased by many effectors and pathways. On the other hand, such peptide-MHC complexes are unique starting points for therapeutic intervention. We present strategies for eliciting an anti-tumoral response by T-cell receptor-based fusion proteins with interleukin (IL)2 and antibody constant region domains, superantigens, and T-cell recruiting antibodies, as well as using genetically modified autologous T-cells as effectors. Another strategy is to direct peptide-MHC complexes to tumors as fusion proteins with an antibody-derived targeting moiety. Finally, we describe T-cell receptor-mimicking antibodies and antibody conjugates as anti tumoral agents.
肿瘤相关抗原可呈递为与主要组织相容性复合体(MHC)分子形成复合物的肽段,这些复合物与T细胞受体相互作用,从而产生免疫抗肿瘤反应。然而,不幸的是,这种反应会受到多种效应因子和信号通路的抑制。另一方面,此类肽-MHC复合物是治疗干预的独特切入点。我们提出了一些策略,包括利用含白细胞介素(IL)-2和抗体恒定区结构域的基于T细胞受体的融合蛋白、超抗原和T细胞募集抗体引发抗肿瘤反应,以及使用基因改造的自体T细胞作为效应细胞。另一种策略是将肽-MHC复合物作为带有抗体衍生靶向部分的融合蛋白导向肿瘤。最后,我们描述了模拟T细胞受体的抗体和抗体偶联物作为抗肿瘤药物。