Cd8 T‐cell recognition of human 5T4 oncofetal antigen

癌胚抗原 埃利斯波特 表位 细胞毒性T细胞 抗原 生物 CD8型 免疫疗法 肿瘤抗原 免疫学 癌症研究 人类白细胞抗原 T细胞 免疫系统 体外 肿瘤相关抗原 生物化学
作者
Lesley A. Smyth,Eyad Elkord,Taher E.I. Taher,Hui-Rong Jiang,Deborah J. Burt,Alison Clayton,Peter A. van Veelen,Arnoud de Ru,Ferry Ossendorp,Cornelis J.M. Melief,Jan W. Drijfhout,Said Dermime,Robert E. Hawkins,Peter L. Stern
出处
期刊:International Journal of Cancer [Wiley]
卷期号:119 (7): 1638-1647 被引量:26
标识
DOI:10.1002/ijc.22018
摘要

Abstract The 5T4 oncofetal antigen is expressed by a wide variety of human carcinomas, including colorectal, ovarian and gastric carcinomas. The restricted expression of 5T4 on tumor tissues as well as its implication in tumor progression and bad prognosis makes 5T4 a promising new candidate for immunotherapy. An MVA vaccine encoding 5T4 antigen has been successfully evaluated in preclinical studies in a murine tumor model. Here, we report the generation of human CD8 T cells specific for the 5T4 antigen by stimulation with autologous monocyte derived DC infected with a replication defective adenovirus encoding the 5T4 cDNA (Ad5T4). Analysis of several donors confirms a repertoire of such CD8 responses. In a parallel approach, incorporating the results of proteasome‐mediated digestion of 5T4 derived 35‐mer peptides and the potential high affinity epitopes predicted by a computer‐based algorithm, we identified 8 putative HLA‐A*0201‐presented CD8 MHC class I epitopes of 5T4 antigen. Two of these generated specific CD8 T cells after restimulation with peptide loaded autologous DC and assay by cytotoxicity and IFNγ ELISPOT. Moreover these particular peptide generated T cells recognized naturally 5T4 positive tumor cells only if they expressed HLA‐A*0201 as judged by IFNγ ELISPOT or ELISA. Also, HLA‐A*0201 CD8 T cells recognized these peptides in a DC‐Ad5T4 polyclonal response. In conclusion, there is a repertoire of CD8 T cell recognition of 5T4 in normal human donors and some candidate HLA‐A*0201 epitopes have been identified. © 2006 Wiley‐Liss, Inc.

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