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本文引用的文献

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Clinical trials on CIK cells: first report of the international registry on CIK cells (IRCC).CIK 细胞的临床试验:CIK 细胞国际注册处(IRCC)的首次报告。
J Cancer Res Clin Oncol. 2011 Feb;137(2):305-10. doi: 10.1007/s00432-010-0887-7. Epub 2010 Apr 21.
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Dendritic cell-activated cytokine-induced killer cells enhance the anti-tumor effect of chemotherapy on non-small cell lung cancer in patients after surgery.树突状细胞激活的细胞因子诱导的杀伤细胞增强了化疗对非小细胞肺癌患者术后的抗肿瘤作用。
Cytotherapy. 2009;11(8):1076-83. doi: 10.3109/14653240903121252.
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Prospective study of chemotherapy in combination with cytokine-induced killer cells in patients suffering from advanced non-small cell lung cancer.晚期非小细胞肺癌患者化疗联合细胞因子诱导的杀伤细胞的前瞻性研究。
Anticancer Res. 2008 Nov-Dec;28(6B):3997-4002.
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Alloreactivity and anti-tumor activity segregate within two distinct subsets of cytokine-induced killer (CIK) cells: implications for their infusion across major HLA barriers.同种异体反应性和抗肿瘤活性在细胞因子诱导的杀伤(CIK)细胞的两个不同亚群中分离:这对它们跨越主要HLA屏障进行输注的意义。
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CD4 +CD25 + regulatory T cells decreased the antitumor activity of cytokine-induced killer (CIK) cells of lung cancer patients.CD4+CD25+调节性T细胞降低了肺癌患者细胞因子诱导的杀伤(CIK)细胞的抗肿瘤活性。
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Chemotherapy advances in small cell lung cancer.小细胞肺癌的化疗进展
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在单一队列的晚期非小细胞肺癌患者中,树突状细胞激活的 CIK 对化疗治疗的增强抗肿瘤作用。

Enhanced antitumor effects of DC-activated CIKs to chemotherapy treatment in a single cohort of advanced non-small-cell lung cancer patients.

机构信息

Department of Immunology, Tianjin Cancer Institute & Hospital, Tianjin Medical University, Huanhuxi Road, Tiyuanbei, Hexi District, 300060, Tianjin, China.

出版信息

Cancer Immunol Immunother. 2013 Jan;62(1):65-73. doi: 10.1007/s00262-012-1311-8. Epub 2012 Jun 29.

DOI:10.1007/s00262-012-1311-8
PMID:22744010
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11028994/
Abstract

Cytokine-induced killer (CIK) cells show cytolytic activity against tumor. The purpose of this study was to evaluate the antitumor effect of dendritic cell (DC)-activated CIK cells in vitro and their clinical efficacy of DC-activated CIK cells in combination with chemotherapy (abbreviated below as chemotherapy plus DC + CIK) in patients with advanced non-small-cell lung cancer (NSCLC). A paired study was performed between 61 patients treated with chemotherapy alone (group 1) and 61 patients treated with chemotherapy plus DC + CIK cells (group 2). In group 2, 36 patients with adenocarcinoma and 18 patients with squamous cell carcinoma were analyzed for the survival rate. Compared to unstimulated CIK cells, DC-activated CIK cells significantly enhanced antitumor activity, increased the ratio of CD3(+)CD56(+) cells, promoted cell proliferation and lessened cell apoptosis. In the paired study, the 1- and 2-year overall survival rates in group 2 were 57.2 and 27.0 %, which were significantly higher than that of group 1 (37.3 and 10.1 %) (P < 0.05). There was no significant difference in the survival rate between the adenocarcinoma and squamous carcinoma patients in group 2. The present study suggests that DC-activated CIK cell has enhanced antitumor effects and chemotherapy plus DC + CIK cells improved the clinical outcomes of chemotherapy for advanced NSCLC patients.

摘要

细胞因子诱导的杀伤(CIK)细胞对肿瘤具有细胞溶解活性。本研究旨在评估树突状细胞(DC)激活的 CIK 细胞在体外的抗肿瘤作用及其在晚期非小细胞肺癌(NSCLC)患者中与化疗联合应用(简称化疗加 DC+CIK)的临床疗效。对 61 例单独接受化疗的患者(第 1 组)和 61 例接受化疗加 DC+CIK 细胞治疗的患者(第 2 组)进行了配对研究。在第 2 组中,对 36 例腺癌患者和 18 例鳞癌患者进行了生存率分析。与未刺激的 CIK 细胞相比,DC 激活的 CIK 细胞显著增强了抗肿瘤活性,增加了 CD3+CD56+细胞的比例,促进了细胞增殖并减少了细胞凋亡。在配对研究中,第 2 组的 1 年和 2 年总生存率分别为 57.2%和 27.0%,明显高于第 1 组(37.3%和 10.1%)(P<0.05)。第 2 组中腺癌和鳞癌患者的生存率无显著差异。本研究表明,DC 激活的 CIK 细胞具有增强的抗肿瘤作用,化疗加 DC+CIK 细胞改善了晚期 NSCLC 患者化疗的临床结局。