Literature DB >> 19120973

A WT1 protein-derived, naturally processed 16-mer peptide, WT1(332), is a promiscuous helper peptide for induction of WT1-specific Th1-type CD4(+) T cells.

Fumihiro Fujiki1, Yoshihiro Oka, Mai Kawakatsu, Akihiro Tsuboi, Hiroko Nakajima, Olga A Elisseeva, Yukie Harada, Zheyu Li, Naoko Tatsumi, Eriko Kamino, Toshiaki Shirakata, Sumiyuki Nishida, Yuki Taniguchi, Ichiro Kawase, Yusuke Oji, Haruo Sugiyama.   

Abstract

The Wilms' tumor gene WT1 is overexpressed in various tumors, and the WT1 protein has been demonstrated to be an attractive target antigen for cancer immunotherapy. A WT1 protein-derived 16-mer peptide, WT1(332) (KRYFKLSHLQMHSRKH), which was naturally generated through processing in cells and could elicit Th1-type CD4(+) helper T cell responses with an HLA-DRB1*0405-restriction has previously been identified by us. In the present study, it has been demonstrated that WT1(332) can induce WT1(332)-specific CD4(+) T cell responses with the restriction of not only HLA-DRB1*0405 but also HLA-DRB1*1501, -DRB1*1502, or -DPB1*0901. These HLA class II-restricted WT1(332)-specific CD4(+) T cell lines produced IFN-gamma but neither IL-4 nor IL-10 with WT1(332) stimulation, thus showing a Th1-type cytokine profile. Furthermore, HLA-DRB1*1501 or -DRB1*1502-restricted WT1(332)-specific CD4(+) T cell lines responded to WT1-expressing transformed cells in an HLA-DRB1-restricted manner, which is consistent with our previous finding that WT1(332) is a naturally processed peptide. These results indicate that the natural peptide, WT1(332), is a promiscuous WT1-specific helper epitope. WT1(332) is expected to apply to cancer patients with various types of HLA class II as a WT1-specific helper peptide in combination with HLA class I-restricted WT1 peptides.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 19120973     DOI: 10.1111/j.1348-0421.2008.00080.x

Source DB:  PubMed          Journal:  Microbiol Immunol        ISSN: 0385-5600            Impact factor:   1.955


  5 in total

1.  Identification of two distinct populations of WT1-specific cytotoxic T lymphocytes in co-vaccination of WT1 killer and helper peptides.

Authors:  Fumihiro Fujiki; Akihiro Tsuboi; Soyoko Morimoto; Naoya Hashimoto; Miki Inatome; Hiroko Nakajima; Jun Nakata; Sumiyuki Nishida; Kana Hasegawa; Naoki Hosen; Yoshihiro Oka; Yusuke Oji; Shinji Sogo; Haruo Sugiyama
Journal:  Cancer Immunol Immunother       Date:  2020-07-22       Impact factor: 6.968

2.  Dendritic cell vaccination as postremission treatment to prevent or delay relapse in acute myeloid leukemia.

Authors:  Sébastien Anguille; Ann L Van de Velde; Evelien L Smits; Viggo F Van Tendeloo; Gunnar Juliusson; Nathalie Cools; Griet Nijs; Barbara Stein; Eva Lion; Ann Van Driessche; Irma Vandenbosch; Anke Verlinden; Alain P Gadisseur; Wilfried A Schroyens; Ludo Muylle; Katrien Vermeulen; Marie-Berthe Maes; Kathleen Deiteren; Ronald Malfait; Emma Gostick; Martin Lammens; Marie M Couttenye; Philippe Jorens; Herman Goossens; David A Price; Kristin Ladell; Yoshihiro Oka; Fumihiro Fujiki; Yusuke Oji; Haruo Sugiyama; Zwi N Berneman
Journal:  Blood       Date:  2017-08-22       Impact factor: 22.113

3.  Tumor-associated antigens in breast cancer.

Authors:  Carmen Criscitiello
Journal:  Breast Care (Basel)       Date:  2012-08       Impact factor: 2.860

Review 4.  Vaccines as consolidation therapy for myeloid leukemia.

Authors:  Gheath Alatrash; Jeffrey J Molldrem
Journal:  Expert Rev Hematol       Date:  2011-02       Impact factor: 2.929

5.  Generation of diffuse large B cell lymphoma-associated antigen-specific Vα6/Vβ13+T cells by TCR gene transfer.

Authors:  Qingsong Yin; Xianfeng Zha; Lijian Yang; Shaohua Chen; Yubing Zhou; Xiuli Wu; Yangqiu Li
Journal:  J Hematol Oncol       Date:  2011-01-11       Impact factor: 17.388

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.