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In-silico discovery of cancer-specific peptide-HLA complexes for targeted therapy

机译:靶向特异性治疗的癌症特异性肽-HLA复合物的计算机模拟发现

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摘要

BackgroundMajor Histocompatibility Complex (MHC) or Human Leukocyte Antigen (HLA) Class I molecules bind to peptide fragments of proteins degraded inside the cell and display them on the cell surface. We are interested in peptide-HLA complexes involving peptides that are derived from proteins specifically expressed in cancer cells. Such complexes have been shown to provide an effective means of precisely targeting cancer cells by engineered T-cells and antibodies, which would be an improvement over current chemotherapeutic agents that indiscriminately kill proliferating cells. An important concern with the targeting of peptide-HLA complexes is off-target toxicity that could occur due to the presence of complexes similar to the target complex in cells from essential, normal tissues.
机译:背景主要组织相容性复合物(MHC)或人类白细胞抗原(HLA)I类分子与细胞内降解的蛋白质的肽片段结合,并在细胞表面展示。我们对涉及从癌细胞中特异性表达的蛋白质衍生的肽的肽-HLA复合物感兴趣。已经显示出这种复合物提供了通过工程化的T细胞和抗体精确靶向癌细胞的有效手段,这将是对目前不加区别地杀死增殖细胞的化学治疗剂的一种改进。靶向肽-HLA复合物的一个重要问题是脱靶毒性,该脱靶毒性可能是由于必需的正常组织细胞中与靶复合物相似的复合物的存在而发生的。

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