Deng Yong-Jun, Xia Jian-Chuan, Zhou Jun, Wang Qi-Jing, Zhang Peng-Yuan, Zhang Lan-Jun, Rong Tie-Hua
State Key Laboratory of Oncology in South China, Guangzhou, Guangdong, PR China.
Ai Zheng. 2007 Feb;26(2):137-41.
BACKGROUND & OBJECTIVE: Dendritic cells (DCs) are antigen-presenting cells, and DC-based fusion vaccine of DCs with tumor cells can induce specific immune response against tumor cells effectively. This study was to investigate the antitumor immunity efficacy of fusion vaccine of DCs with human esophageal carcinoma EC109 cells in vitro.
Peripheral blood mononuclear cells (PBMCs) from healthy volunteers were isolated, and cultured with recombinant human granulocyte-macrophage colony-stimulating factor (rhGM-CSF) and interleukin-4 (IL-4) to generate DCs. Fusion cells of DCs with EC109 cells were generated by polyethylene glycol (PEG) protocol. The T-cell proliferation response stimulated by DC/EC109 cells was detected by MTT assay. The killing efficacy of cytotoxic T lymphocytes (CTLs), activated by DC/EC109 cells, on EC109 cells was evaluated by LDH assay in vitro, and compared with the killing efficacy on human gastric carcinoma SGC7901 cells and human breast cancer MCF7 cells.
The highest fusion efficiency of DCs with EC109 cells was 22.25%. The stimulating efficacy of DC/EC109 cells on the proliferation of T cells was significantly higher than those of DCs and EC109 cells (P<0.05). DC/EC109 cells induced specific CTLs against EC109 cells, and the killing efficacy of the CTLs was significantly higher for EC109 cells than for SGC7901 cells or MCF7 cells (P<0.05).
C/EC109 fusion vaccine can induce specific antitumor response against EC109 cells effectively.
树突状细胞(DCs)是抗原呈递细胞,基于DCs与肿瘤细胞的融合疫苗可有效诱导针对肿瘤细胞的特异性免疫反应。本研究旨在体外研究DCs与人食管癌EC109细胞融合疫苗的抗肿瘤免疫效果。
分离健康志愿者外周血单个核细胞(PBMCs),用重组人粒细胞-巨噬细胞集落刺激因子(rhGM-CSF)和白细胞介素-4(IL-4)培养以生成DCs。通过聚乙二醇(PEG)法生成DCs与EC109细胞的融合细胞。采用MTT法检测DC/EC109细胞刺激的T细胞增殖反应。通过体外乳酸脱氢酶(LDH)法评估由DC/EC109细胞激活的细胞毒性T淋巴细胞(CTLs)对EC109细胞的杀伤效果,并与对人胃癌SGC7901细胞和人乳腺癌MCF7细胞的杀伤效果进行比较。
DCs与EC109细胞的最高融合效率为22.25%。DC/EC109细胞对T细胞增殖的刺激效果显著高于DCs和EC109细胞(P<0.05)。DC/EC109细胞诱导产生针对EC109细胞的特异性CTLs,且CTLs对EC109细胞的杀伤效果显著高于对SGC7901细胞或MCF7细胞(P<0.05)。
DC/EC109融合疫苗可有效诱导针对EC109细胞的特异性抗肿瘤反应。