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Immunization with a HER-2/neu helper peptide vaccine generates HER-2/neu CD8 T-cell immunity in cancer patients

机译:用HER-2 / neu辅助肽疫苗免疫可在癌症患者中产生HER-2 / neu CD8 T细胞免疫

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摘要

CD4 T-cell help is required during the generation and maintenance of effective antitumor CD8 T cell–mediated immunity. The goal of this study was to determine whether HER-2/neu–specific CD8 T-cell immunity could be elicited using HER-2/neu–derived MHC class II “helper” peptides, which contain encompassed HLA-A2–binding motifs. Nineteen HLA-A2 patients with HER-2/neu–overexpressing cancers received a vaccine preparation consisting of putative HER-2/neu helper peptides p369–384, p688–703, and p971–984. Contained within these sequences are the HLA-A2–binding motifs p369–377, p689–697, and p971–979. After vaccination, the mean peptide-specific T-cell precursor frequency to the HLA-A2 peptides increased in the majority of patients. In addition, the peptide-specific T cells were able to lyse tumors. The responses were long-lived and detectable for more than 1 year after the final vaccination in select patients. These results demonstrate that HER-2/neu MHC class II epitopes containing encompassed MHC class I epitopes are able to induce long-lasting HER-2–specific IFN-γ–producing CD8 T cells.
机译:在产生和维持有效的抗肿瘤CD8 T细胞介导的免疫力过程中,需要CD4 T细胞帮助。这项研究的目的是确定是否可以使用含有HLA-A2结合基序的HER-2 / neu衍生的MHC II类“辅助”肽引发HER-2 / neu特异性CD8 T细胞免疫。 19名患有HER-2 / neu过表达的HLA-A2患者接受了疫苗制剂,其中包括推定的HER-2 / neu辅助肽p369-384,p688-703和p971-984。这些序列中包含HLA-A2结合基序p369–377,p689–697和p971–979。接种疫苗后,大多数患者中HLA-A2肽的平均肽特异性T细胞前体频率增加。另外,肽特异性T细胞能够裂解肿瘤。在选定患者中进行最终疫苗接种后,这种反应是长效的,并且可以检测到超过1年。这些结果表明,包含MHC I类抗原决定簇的HER-2 / neu MHC II类抗原决定簇能够诱导持久产生HER-2特异性IFN-γ的CD8 T细胞。

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