Lin Mao, Liang Shuzhen, Jiang Feng, Xu Jiongyuan, Zhu Weibing, Qian Wei, Hu Yong, Zhou Zhanchun, Chen Jibing, Niu Lizhi, Xu Kecheng, Lv Youyong
Department of Biotherapy Center, Fuda Cancer Hospital, Jinan University School of Medicine, NO. 2 TangDe Xi Rd., Tianhe District, Guangzhou, China; Department of Fuda Cancer Institute, Guangzhou, NO. 2 TangDe Xi Rd., Tianhe District, Guangzhou, China.
Department of Fuda Cancer Institute, Guangzhou, NO. 2 TangDe Xi Rd., Tianhe District, Guangzhou, China.
Immunol Lett. 2017 Mar;183:37-43. doi: 10.1016/j.imlet.2017.01.014. Epub 2017 Jan 29.
Dendritic cells (DCs) and cytokine-induced killer (CIK) cells have both shown activity as immunotherapy in some malignancies. Our aim was to prospective assess the effect of this immunotherapy in patients with stage IV breast cancer. Between Aug 2003 and Dec 2013, we collected 368 patients who met inclusion criteria and divided into immunotherapy group (treatment group: 188 patients) and chemotherapy group (control group: 180 patients). DCs were prepared from the mononuclear cells isolated from patients in the treatment group using IL-2/GM-CSF and were loaded with tumour antigens; CIK cells were prepared by incubating peripheral blood lymphocytes with IL-2, IFN-γ, and CD3 antibodies. After the patients had received low-dose chemotherapy, those in the treatment group also received the DC-CIK therapy, which was repeated four times in a fortnight to form one cycle. At least three cycles of DC-CIK therapy were given. Immune function was measured in treatment group patients' sera. Disease-free survival (DFS) and Overall survival (OS) after the diagnosis of stage IV breast cancer was assessed after a 10-year follow-up. The result demonstrated that immune function is obviously enhanced after DC-CIK therapy. By Cox regression analysis, DC-CIK therapy reduced the risk of disease progression (p<0.01) with an increased OS (p<0.01). After low-dose chemotherapy, active immunization with DC-CIK immunotherapy is a potentially effective approach for the control of tumour growth in stage IV breast cancer patients.
树突状细胞(DCs)和细胞因子诱导的杀伤细胞(CIK)在某些恶性肿瘤中均已显示出作为免疫疗法的活性。我们的目的是前瞻性评估这种免疫疗法对IV期乳腺癌患者的疗效。在2003年8月至2013年12月期间,我们收集了368例符合纳入标准的患者,并将其分为免疫治疗组(治疗组:188例患者)和化疗组(对照组:180例患者)。DCs由治疗组患者分离出的单核细胞使用IL-2/GM-CSF制备,并负载肿瘤抗原;CIK细胞通过将外周血淋巴细胞与IL-2、IFN-γ和CD3抗体孵育制备。患者接受低剂量化疗后,治疗组患者还接受DC-CIK治疗,每两周重复4次以形成一个周期。至少给予三个周期的DC-CIK治疗。检测治疗组患者血清中的免疫功能。在进行10年随访后评估IV期乳腺癌诊断后的无病生存期(DFS)和总生存期(OS)。结果表明,DC-CIK治疗后免疫功能明显增强。通过Cox回归分析,DC-CIK治疗降低了疾病进展风险(p<0.01),并延长了总生存期(p<0.01)。低剂量化疗后,采用DC-CIK免疫疗法进行主动免疫是控制IV期乳腺癌患者肿瘤生长的一种潜在有效方法。