肝细胞癌患者经导管动脉化疗栓塞和酪氨酸激酶抑制剂治疗的免疫效果和预后

IF 2.5 4区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY World Journal of Gastrointestinal Oncology Pub Date : 2024-07-15 DOI:10.4251/wjgo.v16.i7.3256
Yuan Guo, Ru-Chun Li, Weiguo Xia, Xiong Yang, Wen-Bo Zhu, Fang-Ting Li, Hong-Tao Hu, Hai-Liang Li
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Monocytes were co-cultured with LM3 liver cancer cells, and their ability to inhibit cancer cell growth was analyzed using the MTT method and a nude mouse subcutaneous tumorigenesis experiment. Simulated combined therapy was done using an in situ liver cancer C57BL/6 male mouse model, and the immune response of tumor tissues was analyzed using immunohistochemistry.\n RESULTS\n Compared to before combination therapy, the proportion of programmed cell death protein 1 (PD-1)+ mononuclear cells and the number of CD4+ T cells decreased in the TACE + apatinib group, while the number of absolute count of CD4+ and CD8+ T cells increased in the TACE + lenvatinib group. Furthermore, the number of regulatory cells decreased in the TACE + donafenib group, whereas the number of CD8+ T and natural killer cells increased. Additionally, monocytes in the TACE combined with donafenib or lenvatinib groups had a stronger ability to inhibit cancer cell growth than those in the other groups. 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引用次数: 0

摘要

背景经导管动脉化疗栓塞术(TACE)和酪氨酸激酶抑制剂(TKIs)的联合治疗在延长肝细胞癌(HCC)患者生存期方面显示出广阔的前景。TACE和TKIs会影响HCC患者的免疫微环境。目的 确定 TACE 和不同 TKIs 组合对免疫微环境的总体影响和差异。方法 收集213例接受TACE联合阿帕替尼、来伐替尼、索拉非尼或多纳非尼治疗的HCC患者在治疗前后3周的数据和免疫细胞谱检测结果。将单核细胞与 LM3 肝癌细胞共同培养,采用 MTT 法和裸鼠皮下肿瘤发生实验分析其抑制癌细胞生长的能力。使用 C57BL/6 雄性小鼠原位肝癌模型进行模拟联合治疗,并使用免疫组化方法分析肿瘤组织的免疫反应。结果 与联合治疗前相比,TACE+阿帕替尼组的程序性细胞死亡蛋白1(PD-1)+单核细胞比例和CD4+T细胞数量减少,而TACE+来伐替尼组的CD4+和CD8+T细胞绝对数量增加。此外,TACE + 多纳非尼组的调节细胞数量减少,而 CD8+ T 细胞和自然杀伤细胞的数量增加。此外,TACE联合多纳非尼或来伐替尼组的单核细胞抑制癌细胞生长的能力强于其他组。TACE 与多纳非尼或来伐替尼联合治疗可增加 CD8+ T 细胞对肿瘤组织的浸润。此外,CD8+细胞中的PD-1+比例、CD8+ T淋巴细胞绝对数和调节性T细胞比例是影响HCC患者生存时间的独立预后因素。结论 TACE 与不同的 TKIs 联用会产生不同的免疫反应。具体来说,TACE与多纳非尼或来伐替尼联合可诱导强烈的抗肿瘤免疫反应。
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Immune effect and prognosis of transcatheter arterial chemoembolization and tyrosine kinase inhibitors therapy in patients with hepatocellular carcinoma
BACKGROUND The combination of transcatheter arterial chemoembolization (TACE) and tyrosine kinase inhibitors (TKIs) has shown broad prospects in prolonging the survival of patients with hepatocellular carcinoma (HCC). TACE and TKIs can affect the immune microenvironment in patients with HCC. AIM To determine the overall effects and differences between TACE and different TKIs combinations on the immune microenvironment. METHODS Data and immune cell profile test results from 213 HCC patients treated with TACE combined with apatinib, lenvatinib, sorafenib, or donafenib before and after 3 wk of treatment were collected. Monocytes were co-cultured with LM3 liver cancer cells, and their ability to inhibit cancer cell growth was analyzed using the MTT method and a nude mouse subcutaneous tumorigenesis experiment. Simulated combined therapy was done using an in situ liver cancer C57BL/6 male mouse model, and the immune response of tumor tissues was analyzed using immunohistochemistry. RESULTS Compared to before combination therapy, the proportion of programmed cell death protein 1 (PD-1)+ mononuclear cells and the number of CD4+ T cells decreased in the TACE + apatinib group, while the number of absolute count of CD4+ and CD8+ T cells increased in the TACE + lenvatinib group. Furthermore, the number of regulatory cells decreased in the TACE + donafenib group, whereas the number of CD8+ T and natural killer cells increased. Additionally, monocytes in the TACE combined with donafenib or lenvatinib groups had a stronger ability to inhibit cancer cell growth than those in the other groups. Combining TACE with donafenib or lenvatinib increased CD8+ T cell infiltration into the tumor tissue. In addition, the proportion of PD-1+ in CD8+ cells, absolute CD8+ T lymphocyte count, and regulatory T cells proportion were independent prognostic factors affecting the survival time of patients with HCC. CONCLUSION TACE, in combination with different TKIs, produces different immune responses. Specifically, TACE combined with donafenib or lenvatinib may induce strong anti-tumor immune responses.
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来源期刊
World Journal of Gastrointestinal Oncology
World Journal of Gastrointestinal Oncology Medicine-Gastroenterology
CiteScore
4.20
自引率
3.30%
发文量
1082
期刊介绍: The World Journal of Gastrointestinal Oncology (WJGO) is a leading academic journal devoted to reporting the latest, cutting-edge research progress and findings of basic research and clinical practice in the field of gastrointestinal oncology.
期刊最新文献
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