| Literature DB >> 12894852 |
Yoshihiro Oka1, Akihiro Tsuboi, Masaki Murakami, Manabu Hirai, Nobuhiko Tominaga, Hiroko Nakajima, Olga A Elisseeva, Tomoki Masuda, Akiko Nakano, Manabu Kawakami, Yusuke Oji, Kazuhiro Ikegame, Naoki Hosen, Keiko Udaka, Masaki Yasukawa, Hiroyasu Ogawa, Ichiro Kawase, Haruo Sugiyama.
Abstract
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.Entities:
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Year: 2003 PMID: 12894852 DOI: 10.1007/bf02983241
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490