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经动脉化疗栓塞与酪氨酸激酶抑制剂治疗肝细胞癌患者的免疫效应及预后

Immune effect and prognosis of transcatheter arterial chemoembolization and tyrosine kinase inhibitors therapy in patients with hepatocellular carcinoma.

作者信息

Guo Yuan, Li Ru-Chun, Xia Wei-Li, Yang Xiong, Zhu Wen-Bo, Li Fang-Ting, Hu Hong-Tao, Li Hai-Liang

机构信息

Department of Minimal Invasive Intervention, The Affiliated Cancer Hospital of Zhengzhou University, Henan Cancer Hospital, Zhengzhou 450003, Henan Province, China.

Department of Radiology, The Affiliated Cancer Hospital of Zhengzhou University, Henan Cancer Hospital, Zhengzhou 450003, Henan Province, China.

出版信息

World J Gastrointest Oncol. 2024 Jul 15;16(7):3256-3269. doi: 10.4251/wjgo.v16.i7.3256.

Abstract

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 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.

摘要

背景

经动脉化疗栓塞术(TACE)与酪氨酸激酶抑制剂(TKIs)联合应用在延长肝细胞癌(HCC)患者生存期方面展现出广阔前景。TACE和TKIs可影响HCC患者的免疫微环境。

目的

确定TACE与不同TKIs联合应用对免疫微环境的总体影响及差异。

方法

收集213例接受TACE联合阿帕替尼、仑伐替尼、索拉非尼或多纳非尼治疗的HCC患者在治疗前及治疗3周后的资料和免疫细胞谱检测结果。将单核细胞与LM3肝癌细胞共培养,采用MTT法和裸鼠皮下成瘤实验分析其抑制癌细胞生长的能力。利用肝癌C57BL/6雄性小鼠模型进行模拟联合治疗,采用免疫组化法分析肿瘤组织的免疫反应。

结果

与联合治疗前相比,TACE+阿帕替尼组程序性细胞死亡蛋白1(PD-1)+单核细胞比例及CD4+T细胞数量减少,而TACE+仑伐替尼组CD4+和CD8+T细胞绝对计数增加。此外,TACE+多纳非尼组调节性细胞数量减少,而CD8+T细胞和自然杀伤细胞数量增加。另外,TACE联合多纳非尼或仑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与多纳非尼或仑伐替尼联合应用可增加CD8+T细胞向肿瘤组织的浸润。此外,CD8+细胞中PD-1+比例、CD8+T淋巴细胞绝对计数及调节性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TKIs联合应用会产生不同的免疫反应。具体而言,TACE联合多纳非尼或仑伐替尼可能诱导较强的抗肿瘤免疫反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1cb/11271774/3146b6c399c6/WJGO-16-3256-g001.jpg

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