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PMID: 27170523 Published · ppublish English Clinical Trial Journal Article

Association of WT1 IgG antibody against WT1 peptide with prolonged survival in glioblastoma multiforme patients vaccinated with WT1 peptide.

International journal of cancer ·Vol. 139 ·No. 6 ·2016-09-15 ·页码 1391-401

Oji Y, Hashimoto N, Tsuboi A, Murakami Y, Iwai M, Kagawa N, Chiba Y, Izumoto S, Elisseeva O, Ichinohasama R, Sakamoto J, Morita S, Nakajima H, Takashima S, Nakae Y, Nakata J, Kawakami M, Nishida S, Hosen N, Fujiki F, Morimoto S, Adachi M, Iwamoto M, Oka Y, Yoshimine T, Sugiyama H

Abstract

We previously evaluated Wilms' tumor gene 1 (WT1) peptide vaccination in a large number of patients with leukemia or solid tumors and have reported that HLA-A*24:02 restricted, 9-mer WT1-235 peptide (CYTWNQMNL) vaccine induces cellular immune responses and elicits WT1-235-specific cytotoxic T lymphocytes (CTLs). However, whether this vaccine induces humoral immune responses to produce WT1 antibody remains unknown. Thus, we measured IgG antibody levels against the WT1-235 peptide (WT1-235 IgG antibody) in patients with glioblastoma multiforme (GBM) receiving the WT1 peptide vaccine. The WT1-235 IgG antibody, which was undetectable before vaccination, became detectable in 30 (50.8%) of a total of 59 patients during 3 months of WT1 peptide vaccination. The dominant WT1-235 IgG antibody subclass was Th1-type, IgG1 and IgG3 . WT1-235 IgG antibody production was significantly and positively correlated with both progression-free survival (PFS) and overall survival (OS). Importantly, the combination of WT1-235 IgG antibody production and positive delayed type-hypersensitivity (DTH) to the WT1-235 peptide was a better prognostic marker for long-term OS than either parameter alone. These results suggested that WT1-235 peptide vaccination induces not only WT1-235-specific CTLs as previously described but also WT1-235-specific humoral immune responses associated with antitumor cellular immune response. Our results indicate that the WT1 IgG antibody against the WT1 peptide may be a useful predictive marker, with better predictive performance in combination with DTH to WT1 peptide, and provide a new insight into the antitumor immune response induction in WT1 peptide vaccine-treated patients.

Keywords
WT1 IgG antibody WT1 peptide-based immunotherapy glioblastoma predictive marker
MeSH 主题词
Adult Aged Biomarkers Cancer Vaccines/administration & dosage,immunology Cell Line, Tumor Combined Modality Therapy Enzyme-Linked Immunosorbent Assay Female Glioblastoma/immunology,mortality,therapy HLA-A24 Antigen/immunology Humans Immunoglobulin G/blood,immunology Immunotherapy Male Middle Aged Peptides/administration & dosage,immunology Prognosis T-Lymphocytes, Cytotoxic/immunology,metabolism Th1 Cells/immunology,metabolism Treatment Outcome Vaccination WT1 Proteins/chemistry,immunology Young Adult
化学物质
Biomarkers Cancer Vaccines HLA-A*24:02 antigen HLA-A24 Antigen Immunoglobulin G Peptides WT1 Proteins
作者与单位
共 26 位作者,点击展开单位 / ORCID
Oji Yusuke
Department of Cancer Stem Cell Biology, Osaka University Graduate School of Medicine, Osaka, Japan.
Hashimoto Naoya
Department of Neurosurgery, Osaka University Graduate School of Medicine, Osaka, Japan.
Tsuboi Akihiro
Department of Cancer Immunotherapy, Osaka University Graduate School of Medicine, Osaka, Japan.
Murakami Yui
Department of Cancer Stem Cell Biology, Osaka University Graduate School of Medicine, Osaka, Japan.
Iwai Miki
Department of Cancer Stem Cell Biology, Osaka University Graduate School of Medicine, Osaka, Japan.
Kagawa Naoki
Department of Neurosurgery, Osaka University Graduate School of Medicine, Osaka, Japan.
Chiba Yasuyoshi
Department of Neurosurgery, Osaka University Graduate School of Medicine, Osaka, Japan.
Izumoto Shuichi
Department of Neurosurgery, Kinki University, Osaka, Japan.
Elisseeva Olga
Cell Signal Unit, Okinawa Institute of Science and Technology, Okinawa, Japan.
Ichinohasama Ryo
Department of Hematology, Tohoku University, Miyagi, Japan.
Sakamoto Junichi
Tokai Central Hospital, Aichi, Japan.
Morita Satoshi
Department of Biomedical Statistics and Bioinformatics, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Nakajima Hiroko
Department of Cancer Immunology, Osaka University Graduate School of Medicine, Osaka, Japan.
Takashima Satoshi
Respiratory Medicine and Allergy, Rheumatic Disease, Osaka University Graduate School of Medicine, Osaka, Japan.
Nakae Yoshiki
Respiratory Medicine and Allergy, Rheumatic Disease, Osaka University Graduate School of Medicine, Osaka, Japan.
Nakata Jun
Department of Cancer Immunotherapy, Osaka University Graduate School of Medicine, Osaka, Japan.
Kawakami Manabu
Department of Cancer Immunotherapy, Osaka University Graduate School of Medicine, Osaka, Japan.
Nishida Sumiyuki
Respiratory Medicine and Allergy, Rheumatic Disease, Osaka University Graduate School of Medicine, Osaka, Japan.
Hosen Naoki
Department of Cancer Stem Cell Biology, Osaka University Graduate School of Medicine, Osaka, Japan.
Fujiki Fumihiro
Department of Cancer Immunology, Osaka University Graduate School of Medicine, Osaka, Japan.
Morimoto Soyoko
Department of Cancer Immunology, Osaka University Graduate School of Medicine, Osaka, Japan.
Adachi Mayuko
Department of Cancer Stem Cell Biology, Osaka University Graduate School of Medicine, Osaka, Japan.
Iwamoto Masahiro
Department of Cancer Stem Cell Biology, Osaka University Graduate School of Medicine, Osaka, Japan.
Oka Yoshihiro
Department of Cancer Immunology, Osaka University Graduate School of Medicine, Osaka, Japan. | Respiratory Medicine and Allergy, Rheumatic Disease, Osaka University Graduate School of Medicine, Osaka, Japan. | Department of Immunopathology, Immunology Frontier Research Center (World Premier International Research Center), Osaka University, Osaka, Japan.
Yoshimine Toshiki
Department of Neurosurgery, Osaka University Graduate School of Medicine, Osaka, Japan.
Sugiyama Haruo
Department of Cancer Immunology, Osaka University Graduate School of Medicine, Osaka, Japan.
Article Info
Journal
International journal of cancer
Abbr.
Int J Cancer
ISSN
1097-0215
Published
2016-09-15
电子出版
2016-00-31
页码
1391-401
Language
English
Country/Region
United States
NLM ID
0042124
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