首页> 美国卫生研究院文献>Cancer Immunity >LUD 00-009: Phase 1study of intensive course immunization with NY-ESO-1 peptides inHLA-A2 positive patients with NY-ESO-1-expressing cancer
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LUD 00-009: Phase 1study of intensive course immunization with NY-ESO-1 peptides inHLA-A2 positive patients with NY-ESO-1-expressing cancer

机译:LUD 00-009:第1阶段NY-ESO-1肽强化过程免疫的研究HLA-A2阳性表达NY-ESO-1的癌症患者

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摘要

NY-ESO-1 is a cancer-testis antigen and an attractive target for immunotherapy in patients with different malignancies. Here we report the results of a phase I clinical study of intensive course NY-ESO-1 peptide vaccination, evaluating the safety, immunogenicity and clinical response in HLA-A2 positive patients with NY-ESO-1 expressing cancers. Of 20 patients enrolled in the trial, 14 completed at least 2 cycles of immunization and were evaluable for clinical and immunological response. Five of these evaluable patients were treated in cohort 1 (baseline seropositive) and 9 patients were treated in cohort 2 (baseline seronegative). During vaccination, NY-ESO-1-specific CD8+ T-cells were induced in 3 of 9 baseline seronegative patients. In patients with pre-existing antigen-specific CD8+ T-cells, their number increased or remained stable. In contrast to previous immunization protocols with less intensive immunization schedules, we observed a rapid induction of high magnitude NY-ESO-1 peptide-specific T-cell responses detectable already on day 15-22 of immunization. A specific immune response of high magnitude and early onset may be more effectivein eliminating minimal residual disease in adjuvant treatment situationsand in preventing tumor progression due to immune escape mechanisms.
机译:NY-ESO-1是一种癌症睾丸抗原,是具有不同恶性肿瘤的患者进行免疫治疗的有吸引力的靶标。在这里,我们报告了强化课程NY-ESO-1肽疫苗接种的I期临床研究结果,评估了表达NY-ESO-1的HLA-A2阳性患者的安全性,免疫原性和临床反应。在该试验的20名患者中,有14名完成了至少2个免疫周期,可以评估其临床和免疫应答。这些可评估的患者中有5名在队列1(基线血清阳性)中接受治疗,9例在队列2(基线血清阴性)中接受治疗。在接种疫苗期间,在9名基线血清阴性患者中的3名中诱导了NY-ESO-1特异性CD8 + T细胞。在已有抗原特异性CD8 + T细胞的患者中,其数量增加或保持稳定。与以前的免疫方案相比,免疫方案的强度较低,我们观察到在免疫的第15-22天就已经可以检测到快速诱导的高强度NY-ESO-1肽特异性T细胞应答。高度特异性和早期发作的特异性免疫反应可能更有效消除辅助治疗情况下的最小残留疾病以及通过免疫逃逸机制防止肿瘤进展。

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