Oka Yoshihiro, Tsuboi Akihiro, Murakami Masaki, Hirai Manabu, Tominaga Nobuhiko, Nakajima Hiroko, Elisseeva Olga A, Masuda Tomoki, Nakano Akiko, Kawakami Manabu, Oji Yusuke, Ikegame Kazuhiro, Hosen Naoki, Udaka Keiko, Yasukawa Masaki, Ogawa Hiroyasu, Kawase Ichiro, Sugiyama Haruo
Department of Molecular Medicine, Osaka University Medical School, Suita City, Osaka, Japan.
Int J Hematol. 2003 Jul;78(1):56-61. doi: 10.1007/BF02983241.
The Wilms tumor gene, WT1, is overexpressed not only in leukemias and myelodysplastic syndrome (MDS) but also in various types of solid tumors, including lung and breast cancer, and the WT1 protein is a tumor antigen for these malignancies. In clinical trials of WT1 peptide-based cancer immunotherapy, patients with overt leukemia from MDS or MDS with myelofibrosis were injected intradermally with 0.3 mg of an HLA-A*2402-restricted, 9-mer WT1 peptide emulsified with Montanide ISA51 adjuvant. Only a single dose of WT1 vaccination resulted in an increase in WT1-specific cytotoxic T-lymphocytes, which was followed by a rapid reduction in leukemic blast cells. Severe leukopenia and local erythema at the injection sites of WT1 peptide were observed as adverse effects. These results have provided us with the first clinical evidence suggesting that WT1 peptide-based immunotherapy is an attractive treatment for patients with leukemias or MDS.
肾母细胞瘤基因WT1不仅在白血病和骨髓增生异常综合征(MDS)中过度表达,在包括肺癌和乳腺癌在内的各种实体瘤中也过度表达,并且WT1蛋白是这些恶性肿瘤的肿瘤抗原。在基于WT1肽的癌症免疫治疗临床试验中,将0.3毫克与Montanide ISA51佐剂乳化的HLA-A*2402限制性9聚体WT1肽皮内注射给患有明显MDS白血病或伴有骨髓纤维化的MDS患者。仅单剂量的WT1疫苗接种就导致WT1特异性细胞毒性T淋巴细胞增加,随后白血病原始细胞迅速减少。观察到WT1肽注射部位出现严重白细胞减少和局部红斑等不良反应。这些结果为我们提供了首个临床证据,表明基于WT1肽的免疫治疗对白血病或MDS患者是一种有吸引力的治疗方法。