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TARGET PEPTIDES FOR OVARIAN CANCER IMMUNOTHERAPY

机译:卵巢癌免疫治疗的靶标肽

摘要

TADG-12 and CA125 are two proteins expressed with high specificity in ovarian cancer tumors. They thus would be potential antigens for immunotherapy in ovarian cancer. The invention is based on the discovery of peptides in TADG-12 and CA125 that can be used to induce an autologous T cell response that lyses ovarian cancer cells expressing TADG-12 or CA125. The peptides are contacted with dendritic cells in vitro to generate peptide-loaded dendritic cells. The peptide-loaded dendritic cells are contacted with T cells in vitro to amplify CD8+ T cells that recognize the peptide. At least one CA 125 peptide and at least one TADG-12 peptide were found that amplified CD8+ T cells, even from cancer patients, that lysed autologous CA125-expressing or TADG-12-expressing tumor cells. The peptide-loaded dendritic cells can be administered to a cancer patient to amplify CD8+ T cells in vivo that attack the cancer cells. Alternatively, autologous CD8+ T cells can be amplified ex vivo and then infused into the cancer patient.
机译:TADG-12和CA125是在卵巢癌肿瘤中高特异性表达的两种蛋白质。因此,它们将是卵巢癌免疫治疗的潜在抗原。本发明基于在TADG-12和CA125中的肽的发现,所述肽可用于诱导自体T细胞应答,所述自体T细胞应答裂解表达TADG-12或CA125的卵巢癌细胞。肽在体外与树突状细胞接触以产生载有肽的树突状细胞。将负载肽的树突细胞在体外与T细胞接触,以扩增识别该肽的CD8 + T细胞。发现至少一种CA 125肽和至少一种TADG-12肽甚至从癌症患者中扩增出的CD8 + T细胞裂解了自体表达CA125或表达TADG-12的肿瘤细胞。可以将载有肽的树突细胞给予癌症患者以在体内扩增攻击癌细胞的CD8 + T细胞。或者,可以将自身CD8 + T细胞离体扩增,然后注入癌症患者体内。

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