Wilms tumor gene peptide-based immunotherapy for patients with overt leukemia from myelodysplastic syndrome (MDS) or MDS with myelofibrosis

被引:107
作者
Oka, Y
Tsuboi, A
Murakami, M
Hirai, M
Tominaga, N
Nakajima, H
Elisseeva, OA
Masuda, T
Nakano, A
Kawakami, M
Oji, Y
Ikegame, K
Hosen, N
Udaka, K
Yasukawa, M
Ogawa, H
Kawase, L
Sugiyama, H
机构
[1] Osaka Univ, Sch Med, Dept Clin Lab Sci, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Sch Med, Dept Mol Med, Suita, Osaka 5650871, Japan
[3] Osaka City Gen Hosp, Osaka, Japan
[4] Suita Municipal Hosp, Osaka, Japan
[5] Kochi Med Sch, Dept Immunol, Kochi, Japan
[6] Ehime Univ, Sch Med, Dept Internal Med 1, Matsuyama, Ehime 790, Japan
关键词
Wilms tumor gene; WT1; immunotherapy; CTL; MDS;
D O I
10.1007/BF02983241
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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. (C) 2003 The Japanese Society of Hematology.
引用
收藏
页码:56 / 61
页数:6
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