Liu Yanfeng, Liu Haibo, Liu Hausheng, He Pengcheng, Li Jing, Liu Xin, Chen Limei, Wang Mengchang, Xi Jiejing, Wang Huaiyu, Zhang Haitao, Zhu Ying, Zhu Wei, Ning Jing, Guo Caili, Sun Chunhong, Zhang Mei
Department of Hematology, The First Affiliated Hospital, Xi'an Jiaotong University, Xi'an, Shaanxi 710061, P.R. China; Department of Hematology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, P.R. China.
Department of Hematology, The First Affiliated Hospital, Xi'an Jiaotong University, Xi'an, Shaanxi 710061, P.R. China; Biological Immune Therapy Center, The First Affiliated Hospital, Xi'an Jiaotong University, Xi'an, Shaanxi 710061, P.R. China.
Oncol Lett. 2016 Dec;12(6):5205-5210. doi: 10.3892/ol.2016.5337. Epub 2016 Nov 2.
Individuals >65 years old account for a large proportion of cancer patients, and usually have poor prognoses due to relative weaker physiological function and lower drug tolerance. To characterize the efficacy and safety of dendritic cell (DC)-activated cytokine-induced killer cell (CIK)-mediated treatment, and develop an adoptive immunotherapy for cancer patients >65 years old, a retrospective study was performed in 58 cancer sufferers who received 1-4 cycles of DC-activated CIK (DC-CIK) treatment and evaluated the response (tumor remission rate) and toxicity (side effects to the treatment). The present results showed that DCs and CIKs could be expanded rapidly , and following co-culture with DCs, the population of cluster of differentiation (CD) 3, CD3CD4, CD3CD8 and CD3CD56 CIKs was significantly increased compared to CIKs without DC activation (P=0.044). In addition, DC-CIK infusion produced marked clinical outcomes, resulting in an objective remission rate, overall clinical benefit rate and Karnofsky performance status of 44.83, 75.86 and 87.28±5.46%, respectively, which was significantly improved compared with prior to treatment (P<0.05). Additionally, subsequent to two cycles of this immunotherapy, several tumor marker expression levels declined, returning to the normal range. The proportion of CD3CD4 (P=0.017) and CD3CD8 (P=0.023) lymphocytes, and the population of CD4/CD8 cells (P=0.024) were also increased. In conclusion, the present study suggests that the immunotherapy mediated by DC-CIK is safe and effective for cancer patients aged >65 years.
65岁以上的个体在癌症患者中占很大比例,并且由于生理功能相对较弱和药物耐受性较低,通常预后较差。为了表征树突状细胞(DC)激活的细胞因子诱导的杀伤细胞(CIK)介导的治疗的疗效和安全性,并为65岁以上的癌症患者开发过继性免疫疗法,对58例接受1 - 4个周期DC激活的CIK(DC - CIK)治疗的癌症患者进行了一项回顾性研究,并评估了反应(肿瘤缓解率)和毒性(治疗副作用)。目前的结果表明,DC和CIK可以迅速扩增,并且与DC共培养后,与未被DC激活的CIK相比,分化簇(CD)3、CD3CD4、CD3CD8和CD3CD56 CIK的群体显著增加(P = 0.044)。此外,DC - CIK输注产生了显著的临床结果,客观缓解率、总体临床受益率和卡氏功能状态分别为44.83%、75.86%和87.28±5.46%,与治疗前相比有显著改善(P < 0.05)。此外,在这种免疫疗法的两个周期之后,几种肿瘤标志物表达水平下降,恢复到正常范围。CD3CD4(P = 0.017)和CD3CD8(P = 0.023)淋巴细胞的比例以及CD4/CD8细胞群体(P = 0.024)也增加了。总之,本研究表明DC - CIK介导的免疫疗法对65岁以上的癌症患者是安全有效的。