Department of Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, No. 17 South Lane, Panjiayuan, Chaoyang District, Beijing, 100021, China.
Department of Oncology, Beijing Biohealthcare Biotechnology Co.,Ltd, FL2, Building 3, Park B, Shunyi District Airport High Tech Zoon, Beijing, 101300, China.
Cancer Immunol Immunother. 2019 Jan;68(1):121-130. doi: 10.1007/s00262-018-2257-2. Epub 2018 Oct 10.
Dendritic cell (DC)-based immunotherapies have been created for a broad expanse of cancers, and DC vaccines prepared with Wilms' tumor protein 1 (WT1) peptides have shown great therapeutic efficacy in these diseases. In this paper, we report the results of a phase I/II study of a DC-based vaccination for advanced breast, ovarian, and gastric cancers, and we offer evidence that patients can be effectively vaccinated with autologous DCs pulsed with WT1 peptide. There were ten patients who took part in this clinical study; they were treated biweekly with a WT1 peptide-pulsed DC vaccination, with toxicity and clinical and immunological responses as the principal endpoints. All of the adverse events to DC vaccinations were tolerable under an adjuvant setting. The clinical response was stable disease in seven patients. Karnofsky Performance Scale scores were enhanced, and computed tomography scans revealed tumor shrinkage in three of seven patients. Human leukocyte antigen (HLA)/WT1-tetramer and cytoplasmic IFN-γ assays were used to examine the induction of a WT-1-specific immune response. The immunological responses to DC vaccination were significantly correlated with fewer myeloid-derived suppressor cells (P = 0.045) in the pretreated peripheral blood. These outcomes offered initial clinical evidence that the WT1 peptide-pulsed DC vaccination is a potential treatment for advanced cancer.
树突状细胞(DC)为广泛的癌症而开发的免疫疗法,用 Wilms' 肿瘤蛋白 1(WT1)肽制备的 DC 疫苗在这些疾病中显示出了很好的治疗效果。在本文中,我们报告了一项针对晚期乳腺癌、卵巢癌和胃癌的基于 DC 的疫苗接种的 I/II 期研究结果,并提供了证据表明患者可以用 WT1 肽脉冲自体 DC 进行有效接种。这项临床研究有 10 名患者参与;他们每两周接受一次 WT1 肽脉冲 DC 疫苗接种治疗,主要终点是毒性、临床和免疫反应。所有 DC 疫苗接种的不良反应在辅助治疗下都是可耐受的。7 名患者的临床反应为稳定疾病。Karnofsky 表现量表评分提高,7 名患者中有 3 名计算机断层扫描显示肿瘤缩小。人类白细胞抗原(HLA)/WT1-四聚体和细胞质 IFN-γ 测定用于检查 WT1 特异性免疫反应的诱导。DC 疫苗接种的免疫反应与预处理外周血中髓系来源抑制细胞(MDSC)减少显著相关(P=0.045)。这些结果提供了初步的临床证据,表明 WT1 肽脉冲 DC 疫苗接种是晚期癌症的一种潜在治疗方法。