Occurrence of tumor antigen pRL1a specific CD8 T cells in spleen cells from syngeneic BALB/c, semiallogeneic (BALB/cxC57BL/6)F1 and allogeneic C57BL/6 mice

被引:0
作者
Hata, H
Uenaka, A
Takada, I
Kenjo, A
Takahashi, M
Ono, T
Fujita, T
Nakayama, E
机构
[1] Okayama Univ, Grad Sch Med & Dent, Dept Immunol, Okayama 7008558, Japan
[2] Okayama Univ, Grad Sch Med & Dent, Dept Internal Med, Okayama 7008558, Japan
[3] Fukushima Med Univ, Dept Biochem, Fukushima 9601295, Japan
关键词
cytotoxic T lymphocytes; tetramer; tumor immunity;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We investigated the generation of CD8 cytotoxic T-lymphocytes (CTL) that recognized a dominant pRL1a peptide bound to H-2L(d) molecule on RL male 1 leukemia in spleen cells from RL male 1-bearing, syngeneic BALB/c, semiallogeneic CB6F(1) and allogeneic B6 mice by repetitive in vitro stimulation with RL male I tumor. CD8 T cells in cultures were also analyzed by H-2L(d)/pRL1a tetramer staining. We showed that pRL1a-specific CTL were more efficiently generated in spleen cells from RL male 1-bearing high responder CB6F(1) mice than in low responder BALB/c mice, and this correlated well with the occurrence of H-2L(d)/pRL1a tetramer binding CD8 T cells. Furthermore, we showed that in spleen cells from RL male 1-bearing allogeneic B6 mice, H-2L(d)/pRL1a complex specific CD8 T cells were present at a significant frequency. H-2L(d)/pRL1a recognizing B6 CTL but not BALB/c or CB6F(1) CTL gradually lost CD8 expression on their surface by multiplication of in vitro stimulation.
引用
收藏
页码:1019 / 1025
页数:7
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