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Improved Activation toward Primary Colorectal Cancer Cells by Antigen-Specific Targeting Autologous Cytokine-Induced Killer Cells

机译:抗原特异性靶向自体细胞因子诱导的杀伤细胞对原发性大肠癌细胞的活化作用增强

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摘要

Adoptive therapy of malignant diseases with cytokine-induced killer (CIK) cells showed promise in a number of trials; the activation of CIK cells from cancer patients towards their autologous cancer cells still needs to be improved. Here, we generated CIK cells ex vivo from blood lymphocytes of colorectal cancer patients and engineered those cells with a chimeric antigen receptor (CAR) with an antibody-defined specificity for carcinoembryonic antigen (CEA). CIK cells thereby gained a new specificity as defined by the CAR and showed increase in activation towards CEA+ colon carcinoma cells, but less in presence of CEA cells, indicated by increased secretion of proinflammatory cytokines. Redirected CIK activation was superior by CAR-mediated CD28-CD3ζ than CD3ζ signaling only. CAR-engineered CIK cells from colon carcinoma patients showed improved activation against their autologous, primary carcinoma cells from biopsies resulting in more efficient tumour cell lysis. We assume that adoptive therapy with CAR-modified CIK cells shows improved selectivity in targeting autologous tumour lesions.
机译:细胞因子诱导的杀伤(CIK)细胞对恶性疾病的过继治疗在许多试验中显示出希望。从癌症患者到其自体癌细胞的CIK细胞的激活仍然需要改善。在这里,我们从结直肠癌患者的血液淋巴细胞中离体生成了CIK细胞,并用嵌合抗原受体(CAR)改造了这些细胞,该抗体具有针对癌胚抗原(CEA)的抗体定义的特异性。因此,CIK细胞获得了CAR所定义的新特异性,并显示出对CEA + 结肠癌细胞的激活增加,但是在CEA -细胞存在下却表现出较少促炎细胞因子的分泌。通过CAR介导的CD28-CD3ζ,重定向的CIK激活优于仅CD3ζ信号传导。来自结肠癌患者的CAR工程改造的CIK细胞显示出针对活检的自体原代癌细胞的增强的活化作用,从而导致了更有效的肿瘤细胞裂解。我们假设采用CAR修饰的CIK细胞进行过继治疗在针对自体肿瘤病变方面显示出更高的选择性。

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