Abstract A017: Immunologic efficacy of heat shock protein 105 peptide vaccine in patients with advanced colorectal and esophageal cancer

Yasuhiro Shimizu, T. Yoshikawa, Kojima Takashi, K. Shoda, Kazuto Nosaka, S. Mizuno, S. Wada, Yuki Fujimoto, T. Sasada, Kenichi Kohashi, H. Bando, I. Endo, T. Nakatsura
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Abstract

Purpose: Heat shock protein 105 (HSP105) is overexpressed in a variety of human cancers, including colorectal cancer (CRC) and esophageal cancer (EC). We identified HLA-A24 or A2-restricted HSP105 peptides that can induce HSP105 peptide-specific cytotoxic T lymphocytes (CTLs) (EP1536006, JP5112615, JP5291641, US9,404,925) and curried out a phase I clinical trial of HLA-A24 or A2-restricted HSP105 peptide vaccine in patients with CRC or EC (UMIN ID000017809). In this study, we aimed to demonstrate the immunological efficacy of the novel vaccine. Experimental design: 30 patients (HLA-A24 group; 15 patients, HLA-A2 group; 15 patients) with advanced CRC or EC were enrolled. Two types of vaccine (A24-1 and A24-7 or A2-7 and A2-12) were administered into the patients, matching HLA-types. Immunological responses were analyzed by ex vivo and in vitro IFN-γ ELISPOT assay using peripheral blood mononuclear cells before and after vaccination, and cytokines produced by HSP105-specific CTLs were measured by Cytometric Bead Array assay. We also analyzed the correlation between immunological responses and prognosis. Result: HSP105 peptide vaccines induced HSP105 peptide-specific CTLs in 15 of 30 patients. In HLA-A24 group, there were 7 patients with the induction only in ex vivo and almost all patients (n=13) showed skin reactions of vaccine sites. By contrast, in HLA-A2 group, there were 4 patients with the induction in ex vivo and 6 patients in in vitro, respectively, and only 6 patients with skin reactions of vaccine sites. In all patients, the existence of skin reaction correlated with the induction in ex vivo (p Citation Format: Yasuhiro Shimizu, Toshiaki Yoshikawa, Kojima Takashi, Kayoko Shoda, Kazuto Nosaka, Shoichi Mizuno, Satoshi Wada, Yuki Fujimoto, Tetsuro Sasada, Kenichi Kohashi, Hideaki Bando, Itaru Endo, Tetsuya Nakatsura. Immunologic efficacy of heat shock protein 105 peptide vaccine in patients with advanced colorectal and esophageal cancer [abstract]. In: Proceedings of the Fourth CRI-CIMT-EATI-AACR International Cancer Immunotherapy Conference: Translating Science into Survival; Sept 30-Oct 3, 2018; New York, NY. Philadelphia (PA): AACR; Cancer Immunol Res 2019;7(2 Suppl):Abstract nr A017.
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A017:热休克蛋白105肽疫苗对晚期结直肠癌和食管癌患者的免疫效果
目的:热休克蛋白105 (HSP105)在多种人类癌症中过表达,包括结直肠癌(CRC)和食管癌(EC)。我们鉴定出能够诱导HSP105肽特异性细胞毒性T淋巴细胞(ctl)的HLA-A24或a2限制性HSP105肽(EP1536006, JP5112615, JP5291641, us9404925),并在结直肠癌或EC患者(UMIN ID000017809)中开展了HLA-A24或a2限制性HSP105肽疫苗的I期临床试验。在这项研究中,我们旨在证明这种新型疫苗的免疫功效。实验设计:30例患者(HLA-A24组;HLA-A2组15例;15例晚期结直肠癌或EC患者入组。两种疫苗(A24-1和A24-7或A2-7和A2-12)被注射到患者体内,匹配hla类型。接种前后,采用外周血单个核细胞体外和体外IFN-γ ELISPOT法分析免疫应答,采用流式细胞仪细胞阵列法检测hsp105特异性ctl产生的细胞因子。我们还分析了免疫反应与预后的关系。结果:HSP105肽疫苗在30例患者中诱导了15例HSP105肽特异性ctl。HLA-A24组仅体外诱导7例,几乎所有患者(n=13)均出现疫苗部位皮肤反应。相比之下,HLA-A2组体内诱导4例,体外诱导6例,疫苗部位皮肤反应仅6例。在所有患者中,皮肤反应的存在与体外诱导相关(p引用格式:Yasuhiro Shimizu, Toshiaki Yoshikawa, Kojima Takashi, Kayoko Shoda, Kazuto Nosaka, Shoichi Mizuno, Satoshi Wada, Yuki Fujimoto, Tetsuro Sasada, Kenichi Kohashi, Hideaki Bando, Itaru Endo, Tetsuya Nakatsura)。热休克蛋白105肽疫苗对晚期结直肠癌和食管癌患者的免疫效果[摘要]。第四届CRI-CIMT-EATI-AACR国际癌症免疫治疗会议:将科学转化为生存;2018年9月30日至10月3日;纽约,纽约。费城(PA): AACR;癌症免疫杂志2019;7(2增刊):no A017。
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