Th1-biased humoral immune responses against Wilms tumor gene WT1 product in the patients with hematopoietic malignancies

被引:39
作者
Wu, F
Oka, Y
Tsuboi, A
Elisseeva, OA
Ogata, K
Nakajima, H
Fujiki, F
Masuda, T
Murakami, M
Yoshihara, S
Ikegame, K
Hosen, N
Kawakami, M
Nakagawa, M
Kubota, T
Soma, T
Yamagami, T
Tsukaguchi, M
Ogawa, H
Oji, Y
Hamaoka, T
Kawase, I
Sugiyama, H
机构
[1] Osaka Univ, Grad Sch Med, Dept Funct Diagnost Sci, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Grad Sch Med, Dept Mol Med, Suita, Osaka 5650871, Japan
[3] Osaka Univ, Grad Sch Med, Dept Canc Immunotherapy, Suita, Osaka 5650871, Japan
[4] Nippon Med Coll, Dept Internal Med 3, Tokyo 113, Japan
[5] Nippon Life Saiseikai Fdn, Nissay Hosp, Osaka, Japan
[6] Tondabayashi Hosp, Osaka, Japan
[7] Osaka Minami Natl Hosp, Dept Internal Med, Osaka, Japan
[8] Sakai Municipal Hosp, Osaka, Japan
[9] Osaka Univ, Grad Sch Med, Dept Oncol, Osaka, Japan
关键词
Wilms' tumor gene (WT1); humoral immune response; IgG subclass; Th1; cancer immunotherapy;
D O I
10.1038/sj.leu.2403539
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The Wilms' tumor gene WT1 is highly expressed in leukemias and myelodysplastic syndrome (MDS), and WT1 expression levels increase along with the disease progression in chronic myeloid leukemia and MDS. We previously reported that IgM and IgG WT1 antibodies were detected with significantly higher detection rate and antibody titers in leukemias and MDS compared to those in healthy volunteers. In this study, whether IgG humoral immune responses against WT1 protein were Th1- or Th2-type were determined by measurement of four subclasses of IgG WT1 antibody, IgG1, IgG2, IgG3, and IgG4. In leukemias and MDS, Th1- type WT1 antibodies such as IgG1, IgG2, and IgG3 were significantly increased in both detection rate and antibody titers compared to those in healthy volunteers, whereas Th2-type WT1 antibody such as IgG4 did not increase. These results showed that Th1- biased humoral immune responses against WT1 protein were generated in leukemias and MDS. These results should allow us to consider that Th1- biased cellular immune responses against WT1 protein, which was essentially needed for cancer immunotherapy targeting WT1, should be elicited in patients with hematopoietic malignancies.
引用
收藏
页码:268 / 274
页数:7
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