| GeneLibs

题目:: A potent immunogenic general cancer vaccine that targets survivin, an inhibitor of apoptosis proteins.
作者:: Idenoue(Satomi),Hirohashi(Yoshihiko),Torigoe(Toshihiko),Sato(Yuriko),Tamura(Yasuaki),Hariu(Hiroyuki),Yamamoto(Masaaki),Kurotaki(Takehiro),Tsuruma(Tetsuhiro),Asanuma(Hiroko),Kanaseki(Takayuki),Ikeda(Hideyuki),Kashiwagi(Kiyoteru),Okazaki(Minoru),Sasaki(Kazuaki),Sato(Takashi),Ohmura(Tousei),Hata(Fumitake),Yamaguchi(Koji),Hirata(Koichi),Sato(Noriyuki)
状态:: 发布时间2005-03-04 , 更新时间 2011-11-17
期刊:: Clin Cancer Res
摘要:: We reported previously a HLA-A24-restricted antigenic peptide, survivin-2B80-88 (AYACNTSTL), recognized by CD8(+) CTL. This peptide was derived from survivin protein, an inhibitor of apoptosis proteins, expressed in a variety of tumors, such as adenocarcinoma, squamous cell carcinoma, and malignant melanoma. In this report, we provide further evidence that survivin-2B80-88 peptide might serve as a potent immunogenic cancer vaccine for various cancer patients. Overexpression of survivin was detected in surgically resected primary tumor specimens of most breast and colorectal cancers and some gastric cancers as assessed by immunohistochemical study. HLA-A24/survivin-2B80-88 tetramer analysis revealed that there existed an increased number of CTL precursors in peripheral blood mononuclear cells (PBMC) of HLA-A24(+) cancer patients, and in vitro stimulation of PBMCs from six breast cancer patients with survivin-2B80-88 peptide could lead to increases of the CTL precursor frequency. Furthermore, CTLs specific for this peptide were successfully induced from PBMCs in all 7 (100%) patients with breast cancers, 6 of 7 (83%) patients with colorectal cancers, and 4 of 7 (57%) patients with gastric cancers. These data indicate that survivin expressed in tumor tissues is antigenic in cancer patients, and survivin-2B80-88-specific CTLs are present in PBMCs of various cancer patients. Our study raises the possibility that this peptide may be applicable as a general cancer vaccine to a large proportion of HLA-A24(+) cancer patients.
语言:: eng
DOI:: 10.1158/1078-0432.CCR-03-0817

文献库文献相关信息

DataTable pData

联系方式

微信公众号

文献库 文献相关信息

DataTable pData

联系方式

微信公众号

文献库文献相关信息