题名 | Two novel squamous cell carcinoma antigen-derived HLA-A*0201-binding peptides induce in vitro and in vivo CD8(+) cytotoxic T lymphocyte responses |
作者 | |
发表日期 | 2013-04 |
发表期刊 | INTERNATIONAL JOURNAL OF ONCOLOGY 影响因子和分区 |
语种 | 英语 |
原始文献类型 | Article |
关键词 | squamous cell carcinoma antigen HLA-A*0201 epitope cytotoxic T lymphocytes |
其他关键词 | TUMOR-ANTIGEN ; PROGNOSTIC-SIGNIFICANCE ; HEPATITIS-C ; SCC ANTIGEN ; SERPIN ; CTL ; IDENTIFICATION ; VIRUS ; EPITOPE ; CANCER |
摘要 | Squamous cell carcinoma antigen (SCCA) is over-expressed in many squamous cell cancers and SCCA-derived peptide-specific CD8(+) cytotoxic T lymphocytes can display cytotoxicity against tumor cells. In the present study, we screened the SCCA amino acid sequence for potential HLA-A*0201-binding CD8(+) T-cell epitopes using two predictive computational algorithms. Seven epitope candidates were selected of which SCCA(246-254)(LLPNEIDGL), SCCA(223-231)(SLEDVQAKV), SCCA(328-336)(VLHKAFVEV) and SCCA(324-332)(VLSGVLHKA) significantly stabilized HLA-A*0201 molecules on T2 cells. Both SCCA(328-336) and SCCA(324-332) induced CD8(+) IFN-gamma(+) T-cell responses in HLA-A*0201-positive peripheral blood mononuclear cells as assessed by intracellular cytokine staining. Consistent with this, immunization with either SCCA(328-336) or SCCA(324-332) effectively elicited CD8(+) IFN-gamma(+) T cells in HLA-A*0201 transgenic mice as visualized by IFN-gamma ELISPOT assay and intracellular cytokine staining. Furthermore, CD8(+) T cells induced in vitro or in vivo by SCCA(328-336) or SCCA(324-332) demonstrated in vitro cytotoxicity against peptide-pulsed T2 cells and splenocytes, respectively. These novel SCCA-derived CD8(+) T-cell epitopes described, herein, may be potentially important components for diagnostic reagents and immunotherapeutic vaccines for the treatment of squamous cell carcinomas. |
资助项目 | National Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [30800050, 31070143]; Natural Science Foundation of Zhejiang provinceNatural Science Foundation of Zhejiang Province [Y2090744]; Planned Science and Technology Project of Wenzhou [H20100066, Y20090338] |
出版者 | SPANDIDOS PUBL LTD |
出版地 | ATHENS |
ISSN | 1019-6439 |
EISSN | 1791-2423 |
卷号 | 42期号:4页码:1482-1492 |
DOI | 10.3892/ijo.2013.1834 |
页数 | 11 |
WOS类目 | Oncology |
WOS研究方向 | Oncology |
WOS记录号 | WOS:000316511200042 |
收录类别 | SCIE ; PUBMED ; SCOPUS |
URL | 查看原文 |
PubMed ID | 23426430 |
SCOPUSEID | 2-s2.0-84874594116 |
通讯作者地址 | [Wen, Jin-Sheng]Department of Microbiology and Immunology,Wenzhou Medical College,China |
Scopus学科分类 | Oncology;Cancer Research |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | https://kms.wmu.edu.cn/handle/3ETUA0LF/5667 |
专题 | 检验医学院(生命科学学院、生物学实验教学中心)_病原生物学与免疫学系 附属第二医院 第二临床医学院、附属第二医院、育英儿童医院 基础医学院(机能实验教学中心)_病原生物学与免疫学系_医学寄生虫学 |
通讯作者 | Wen, Jin-Sheng |
作者单位 | 1.Department of Microbiology and Immunology,Wenzhou Medical College,China; 2.Department of Clinical Laboratory,Second Affiliated Hospital,Wenzhou Medical College,China; 3.Department of Parasitology,Wenzhou Medical College,China; 4.Department of Microbiology,Zhongshan Medical School,Sun Yat-Sen University,China; 5.Department of Clinical Laboratory,People's Hospital of Ruian,China |
第一作者单位 | 病原生物学与免疫学系; 附属第二医院 |
通讯作者单位 | 病原生物学与免疫学系 |
第一作者的第一单位 | 病原生物学与免疫学系 |
推荐引用方式 GB/T 7714 | Duan, Zhi-Liang,Wang, Zhi-Bin,Guo, Jiang-Long,et al. Two novel squamous cell carcinoma antigen-derived HLA-A*0201-binding peptides induce in vitro and in vivo CD8(+) cytotoxic T lymphocyte responses[J]. INTERNATIONAL JOURNAL OF ONCOLOGY,2013,42(4):1482-1492. |
APA | Duan, Zhi-Liang., Wang, Zhi-Bin., Guo, Jiang-Long., Liu, Wen-Quan., Hu, Jun., ... & Wen, Jin-Sheng. (2013). Two novel squamous cell carcinoma antigen-derived HLA-A*0201-binding peptides induce in vitro and in vivo CD8(+) cytotoxic T lymphocyte responses. INTERNATIONAL JOURNAL OF ONCOLOGY, 42(4), 1482-1492. |
MLA | Duan, Zhi-Liang,et al."Two novel squamous cell carcinoma antigen-derived HLA-A*0201-binding peptides induce in vitro and in vivo CD8(+) cytotoxic T lymphocyte responses".INTERNATIONAL JOURNAL OF ONCOLOGY 42.4(2013):1482-1492. |
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