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TCR-MHC/肽相互作用:新型抗肿瘤药物的前景

TCR-MHC/peptide interaction: prospects for new anti-tumoral agents.

作者信息

Weidle Ulrich H, Georges Guy, Tiefenthaler Georg

机构信息

Roche Pharma Research and Early Development (pRED), Roche Innovation Center Penzberg, Roche Diagnostics GmbH, Penzberg, Germany.

出版信息

Cancer Genomics Proteomics. 2014 Nov-Dec;11(6):267-77.

Abstract

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.

摘要

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。

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