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同基因BALB/c、半同种异体(BALB/c×C57BL/6)F1和同种异体C57BL/6小鼠脾细胞中肿瘤抗原pRL1a特异性CD8 T细胞的出现情况。

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

作者信息

Hata Hidenori, Uenaka Akiko, Takada Itsuro, Kenjo Akira, Takahashi Minoru, Ono Toshiro, Fujita Teizo, Nakayama Eiichi

机构信息

Department of Immunology, Okayama University Graduate School of Medicine and Dentistry, Okayama 700-8558, Japan.

出版信息

Int J Oncol. 2002 May;20(5):1019-25.

Abstract

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 CB6F1 and allogeneic B6 mice by repetitive in vitro stimulation with RL male 1 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 CB6F1 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 CB6F1 CTL gradually lost CD8 expression on their surface by multiplication of in vitro stimulation.

摘要

我们通过用RL雄性1肿瘤进行重复体外刺激,研究了在携带RL雄性1的同基因BALB/c、半同种异体CB6F1和同种异体B6小鼠的脾细胞中,识别与RL雄性1白血病上H-2L(d)分子结合的显性pRL1a肽的CD8细胞毒性T淋巴细胞(CTL)的产生。培养物中的CD8 T细胞也通过H-2L(d)/pRL1a四聚体染色进行分析。我们发现,与低反应性的BALB/c小鼠相比,在携带RL雄性1的高反应性CB6F1小鼠的脾细胞中能更有效地产生pRL1a特异性CTL,这与H-2L(d)/pRL1a四聚体结合CD8 T细胞的出现密切相关。此外,我们还发现,在携带RL雄性1的同种异体B6小鼠的脾细胞中,H-2L(d)/pRL1a复合物特异性CD8 T细胞以显著频率存在。识别H-2L(d)/pRL1a的B6 CTL,而不是BALB/c或CB6F1 CTL,通过体外刺激增殖会逐渐在其表面失去CD8表达。

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