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MICA表达预测非小细胞肺癌术后化疗联合NK细胞输注治疗的疗效

MICA expression predicts the efficacy of postoperative chemotherapy combined with NK cell infusion in non-small cell lung cancer

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【作者】 周智锋李洁羽林万松陈淑萍王玲叶韵斌郑庆丰

【Author】 ZHOU Zhifeng;LI Jieyu;LIN Wansong;CHEN Shuping;WANG Ling;YE Yunbin;ZHENG Qingfeng;Tumor Immunology Laboratory, Fujian Provincial Key Laboratory of Translational Cancer Medicine, Fujian Cancer Hospital & Fujian Medical University Cancer Hospital;Department of Thoracic Surgery, Fujian Cancer Hospital & Fujian Medical University Cancer Hospital;

【机构】 福建省肿瘤医院福建医科大学附属肿瘤医院福建省肿瘤转化医学重点实验室肿瘤免疫学研究室福建省肿瘤医院福建医科大学附属肿瘤医院胸外科

【摘要】 目的探讨MHC-Ⅰ类相关分子A(MHC classⅠ-related molecules A,MICA)表达是否能预测非小细胞肺癌术后化疗联合NK细胞输注治疗的疗效。方法流式细胞仪检测92例非小细胞肺癌组织MICA表达。非小细胞肺癌患者手术后,单纯化疗41例(多西他赛+顺铂方案)、化疗联合NK细胞治疗51例,单因素与多因素比较临床因素与生存期关系。结果非小细胞肺癌组织46.74%MICA阴性表达,53.26%MICA阳性表达,NK细胞培养14~17 d后NKG2D高达(97.8%±2.5)%,明显高于培养前(88.2%±7.2)%(P<0.05)。MICA是否表达与NKG2D高低无关(P=0.189)。非小细胞肺癌患者术后Ⅱ期患者的3年及5年的生存率分别为70.8%及47.9%,ⅢA期患者的3年及5年的生存率分别为54.5%及22.7%,中位生存期在是否联合NK治疗(P=0.037)及临床分期(TNM)(P=0.009)存在差异,而患者在年龄(P=0.999)、性别(P=0.412)、病理类型(P=0.782)及MICA表达(P=0.172)均无差异。多因素分析显示,中位生存期在是否联合NK治疗(P=0.044)、临床分期(TNM)(P=0.002)及NK与MICA交叉分析(P=0.002)存在差异。结论 MICA在非小细胞肺癌患者术后化疗联合NK细胞免疫治疗中起重要作用,MICA表达可作为NK细胞免疫治疗的预后因素。

【Abstract】 This study was designed to investigate whether MICA expression can predict the efficacy of postoperative chemotherapy combined with NK cell infusion in non-small cell lung cancer(NSCLC). MICA expression in 92 cases lung cancer tissue was evaluated by Flow cytometry, in which 41 patients received adjuvant chemotherapy alone(Docetaxel + Cisplatin) and 51 patients received adjuvant chemotherapy combined with autologous NK cell therapy. Factors associated with survival of patients with non-small cell lung cancer were subjected to univariate and multivariate analysis. Data showed that MICA negative expression of non-small cell lung cancer was 46.74% while MICA positive expression was 53.26%; NKG2 D was up to(97.8% ± 2.5)% after NK cellculture for 14-17 days, which was significantly higher than before culture(88.2% ± 7.2)%(P<0.05). MICA expression was not significantly related to NKG2D(P=0.189). The 3-year and 5-year survival rates of patients with non-small cell lung cancer at stage Ⅱ were 70.8% and 47.9%; the 3-year and 5-year survival rates of patients at stage ⅢA were 54.5% and 22.7%. Median overall survival(mOS) was significantly different in patients treated with or without NK(P=0.037), and in patients with different clinical stages(TNM)(P=0.009), but the mOS showed no correlation with age(P=0.999), gender(P=0.412),pathological type(P=0.782) and MICA expression(P=0.172). Multivariate analysis indicated that NK therapy(P=0.172), and the stage(P=0.002) and the interaction of MICA status and NK therapy(P=0.002) were independent prognostic factors for mOS. Taken together, MICA plays an important role in postoperative chemotherapy combined with NK cell immunotherapy in patients with non-small cell lung cancer, and MICA expression is a good prognostic factor for NK cell immunotherapy.

【关键词】 非小细胞肺癌MICA自然杀伤细胞
【Key words】 Non-small cell lung cancerMICANK cells
【基金】 福建省自然科学基金(2015J01378);国家临床重点专科建设项目(国卫办医涵[2013]544)
  • 【文献出处】 免疫学杂志 ,Immunological Journal , 编辑部邮箱 ,2017年09期
  • 【分类号】R734.2
  • 【被引频次】5
  • 【下载频次】179
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