细胞毒性T细胞
CTL公司*
表位
抗原
细胞毒性
免疫学
CD8型
人类白细胞抗原
生物
病毒学
癌症研究
体外
生物化学
作者
Taichi Azuma,Masanori Makita,Kanji Ninomiya,Shigeru Fujita,Mine Harada,Masaki Yasukawa
标识
DOI:10.1046/j.0007-1048.2001.03329.x
摘要
Summary. We previously reported the establishment of a Wilms' tumour (WT)1‐derived peptide (CMTWNQMNL)‐specific and human leucocyte antigen (HLA)‐A24‐restricted anti‐leukaemia cytotoxic T lymphocyte (CTL) line, TAK‐1. In this study, we have established a novel WT1‐derived peptide (RWPSCQKKF)‐specific CD8 + CTL line, designated NIM‐1. NIM‐1 lysed HLA‐A24‐positive leukaemia cells, but not HLA‐A24‐negative leukaemia cells or normal cells. The effects of TAK‐1 and NIM‐1 on cytotoxicity against leukaemia cells were not synergistic, suggesting that recognition of a single epitope on the tumour‐specific antigen by CTLs is sufficient to exert maximal cytotoxic activity against tumour cells.
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