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作 者:郑培浩[1] 刘毅[1] 岑坚[1] 李莉[1] 赵德峰[1] 沈建良[1]
出 处:《临床军医杂志》2014年第2期124-127,共4页Clinical Journal of Medical Officers
摘 要:目的探讨自体树突状细胞(DCs)联合细胞因子诱导的杀伤细胞(CIK)过继免疫治疗对肾癌和非小细胞肺癌患者免疫功能的影响。方法选取Ⅲ~Ⅳ期肾癌患者28例和Ⅲ-Ⅳ期非小细胞肺癌患者15例,分别于DCs—CIK细胞免疫治疗前和治疗后第30天监测患者免疫功能指标,包括外周血T淋巴细胞亚群以及干扰素-γ(IFN-γ)、肿瘤坏死因子(TNF-α)、白细胞介素-10(IL-10)、IL-6、IL-4、IL-2等细胞因子水平。结果肾癌患者经DCs—CIK治疗后30d与治疗前比较,外周血IFN-γ、IL-2升高(P〈0.05),IL-10降低(P〈0.05),TNF—α、IL-6、IL-4则无明显变化(P〉0.05)。T淋巴细胞亚群中CD3+T细胞、CD3+CD8+T细胞、NKT细胞比例较治疗前有所提高(P〈0.05),而CD3+CD4+T细胞、NK细胞、调节性T细胞(Tregs)则无明显变化(P〉0.05)。非小细胞肺癌患者DCs—CIK治疗后30d与治疗前比较,外周血IFN-γ、IL-2升高(P〈0.05),TNF-α、IL-10、IL-6、IL4则无明显变化(P〉0.05)。T淋巴细胞亚群中CD3+T细胞、CD3+CD8+T细胞、NKT细胞比例较治疗前有所提高,CD3+CD4+T细胞、NK细胞、Treg细胞则无明显变化。结论DCs—CIK细胞免疫治疗能改善晚期肾癌和非小细胞肺癌患者的免疫功能。Objective To investigate the effects of dendritic cells (DCs) combined with cytokine induced killer (CIK) immuno-therapy on the immune function of patients with renal cancer or non-small cell lung cancer. Methods A total of 28 patients with renal cancers and 15 patients with non-small cell lung cancers in stage m - IVof TNM were treated with DCs-CIK immunotherapy. We detected the immunity of the patients including CD3 + , CD4 + and CD8 + T lymphoeytes, NK cells, NKT cells, Treg cells, eytokins (IFN-γ, TNF-oL, IL-10, IL-6, IL-4 and IL-2) in the peripheral blood of the patients before and on the 30th day after the beginning of the immunotherapy. Results On the 30th day after DCs-CIK immunotherapy, the levels of IFN-7 and IL-2 and the ratios of CD3 + T lymphoeytes, CD3 + CD8 + T lymphocytes and NKT cells in the peripheral blood of the patients with renal cancers were more higher than that before ( P 〈 0.05 ). The level of IL-10 was lower after immunotherapy than before ( P 〈 0.05 ). There were no obvious changes in the levels of TNF-α, IL-6, IL-4 and in the ratios of CD3 + CIM + T lymphocytes, NK and Treg cells (P 〉 0.05). On the 30th day after the beginning of immunotherapy, the levels of IFN-γ and IL-2 and the ratios of CD3 + T lymphocytes, CD3 + CD8 + T lymphocytes and NKT cells in the peripheral blood of the patients with non-small cell lung cancers were more higher than that before immunotherapy (P 〈 0.05). There were no obvious changes in the levels of TNF-α, IL-10, IL-6 and IL-4 and in the ratios of CD3 + CD4 + T lymphoeytes, NK cells and Treg cells. Conclusion DCs-CIK immunotherapy can improve the immune function of the patients with advanced renal cancer and non-small cell lung cancer.
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