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超抗原SEA增强PML-RARα多肽体外诱导特异性CTL杀伤活性的机制

林晨, 白雪, 高珂, 杨力建, 陈少华, 李扬秋

林晨, 白雪, 高珂, 杨力建, 陈少华, 李扬秋. 超抗原SEA增强PML-RARα多肽体外诱导特异性CTL杀伤活性的机制[J]. 肿瘤防治研究, 2008, 35(09): 627-629. DOI: 10.3971/j.issn.1000-8578.2477
引用本文: 林晨, 白雪, 高珂, 杨力建, 陈少华, 李扬秋. 超抗原SEA增强PML-RARα多肽体外诱导特异性CTL杀伤活性的机制[J]. 肿瘤防治研究, 2008, 35(09): 627-629. DOI: 10.3971/j.issn.1000-8578.2477
LIN Chen, BAI Xue, GAO Ke, YANG Li-jian, CHEN Shao-hua, LI Yang-qiu. Effects of Staphylococcal Enterotoxin A(SEA) on Cytotoxicity of T Cells Stimulated by PML-RARα Peptide in vitro[J]. Cancer Research on Prevention and Treatment, 2008, 35(09): 627-629. DOI: 10.3971/j.issn.1000-8578.2477
Citation: LIN Chen, BAI Xue, GAO Ke, YANG Li-jian, CHEN Shao-hua, LI Yang-qiu. Effects of Staphylococcal Enterotoxin A(SEA) on Cytotoxicity of T Cells Stimulated by PML-RARα Peptide in vitro[J]. Cancer Research on Prevention and Treatment, 2008, 35(09): 627-629. DOI: 10.3971/j.issn.1000-8578.2477

超抗原SEA增强PML-RARα多肽体外诱导特异性CTL杀伤活性的机制

详细信息
  • 中图分类号: R733. 71 ;73236

Effects of Staphylococcal Enterotoxin A(SEA) on Cytotoxicity of T Cells Stimulated by PML-RARα Peptide in vitro

  • 摘要: 目的探讨超抗原SEA体外增强PML-RARα多肽诱导特异性CTL杀伤活性的机制。方法分别将SEA、PML-RARα多肽以及SEA联合PML-RARα多肽与正常人外周血单个核细胞共同培养,利用CCK-8比色法检测诱导后T细胞对NB4和K562细胞株杀伤活性,同时利用流式细胞术测定诱导T细胞表面CD4与CD8表达情况。结果诱导后第20天,SEA能明显增强PML-RARα多肽特异性杀伤NB4细胞株的作用。诱导后第5、10、20天动态检测表明,多肽及SEA联合多肽组CD4+/CD8+比值逐渐降低,其中SEA联合PML-RARα多肽诱导组降低最显著。结论超抗原SEA能明显增强PML-RARα多肽体外诱导特异性CD8+T细胞的增殖与特异性的杀伤作用。

     

    Abstract: Objective To investigate the Effects of staphylococcal enterotoxin A (SEA) on the cytotoxicity of T cells stimulated by PML-RARα peptide in vitro. Methods Peripheral blood mononuclear cells from healthy donors were cultured with PML-RARα peptide and SEA for 20 days. After induction,the cytotoxicity of T cells induced against NB4 and K562 cell lines were examined by Cell Counting Kit-8 (CCK-8). The CD4 and CD8 surface markers on the harvested CD3+ T cells were detected by flow cytometry (FCM). Results The cytotoxicity of T cells induced by PML-RARα peptide with SEA was higher than that of T cells induced only by PML-RARα peptide against NB4 cells. The FCM assay showed that the ratio of CD4+ / CD8+ T cells were gradually decreased in both groups of PML-RARα peptide whether with SEA or not at the intervals of day 5, 10 and 20 af ter induction, but the most significantly decreased by PML-RARαpeptide with SEA. Conclusion  The specific cytotoxicity of CD8+ T cells induced by PML-RARαpeptide against NB4 cells could be enhanced with superantigen SEA.

     

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出版历程
  • 收稿日期:  2007-09-19
  • 修回日期:  2007-11-13
  • 刊出日期:  2008-09-24

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