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©2008 The WJG Press and Baishideng.
World J Gastroenterol. Dec 14, 2008; 14(46): 7127-7132
Published online Dec 14, 2008. doi: 10.3748/wjg.14.7127
Published online Dec 14, 2008. doi: 10.3748/wjg.14.7127
Figure 4 Generation of tumor-specific cytotoxic T cells ex vivo.
Splenic CD3+ T cells were isolated from naïve B6 mice with MACS. T cells were primed with SGC-7901 tumor cell lysate-pulsed BM-derived DCs as described in Materials and Methods. Unpulsed DCs and SGC-7901 tumor lyastes were used as controls. The primed T cells (effector cells) were titrated by serial dilution (1:1, 5:1, 10:1, 25:1, 50:1, 100:1), and mixied with SGC-7901 or B16 target cells, and their lytic activity against SGC-7901 or B16 was assayed by a Cytotoxicity Detection Kit. Statistical analysis used the paired Student’s t test. The results are representative of three independent experiments. Data are given as mean ± SE. aP < 0.05, SGC-7901 TP DCs primed T cell/SGC-7901 group versus SGC-7901 TP DCs primed T cell/B16 group or other control groups.
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Citation: Li YL, Wu YG, Wang YQ, Li Z, Wang RC, Wang L, Zhang YY. Bone marrow-derived dendritic cells pulsed with tumor lysates induce anti-tumor immunity against gastric cancer
ex vivo . World J Gastroenterol 2008; 14(46): 7127-7132 - URL: https://www.wjgnet.com/1007-9327/full/v14/i46/7127.htm
- DOI: https://dx.doi.org/10.3748/wjg.14.7127