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TCR-MHC/Peptide Interaction: Prospects for New Anti-tumoral Agents

机译:TCR-MHC /肽相互作用:新型抗肿瘤药的前景

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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.
机译:肿瘤相关抗原可作为与主要组织相容性复合物(MHC)分子形成复合物的肽呈现,该分子与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,这种反应可以通过许多效应子和途径来降低。另一方面,这种肽-MHC复合物是治疗干预的独特起点。我们提出了通过白介素(IL)2和抗体恒定区域,超抗原和T细胞募集抗体,以及使用基因修饰的自体T细胞,通过基于T细胞受体的融合蛋白引发抗肿瘤反应的策略作为效应器。另一策略是将肽-MHC复合物作为具有抗体衍生的靶向部分的融合蛋白引导至肿瘤。最后,我们描述了模仿T细胞受体的抗体和抗体缀合物作为抗肿瘤药物。

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