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肝细胞癌的免疫治疗策略:在不久的将来构筑希望的基石

英文原题:Immunotherapeutic approaches in Hepatocellular carcinoma: Building blocks of hope in near future.

查看英文原题

Immunotherapeutic approaches in Hepatocellular carcinoma: Building blocks of hope in near future.

PubMed 2022/12/17(内容时间) Eur J Cell Biol Q2 · IF 4.3(JCR 2025)

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中文摘要

肝细胞癌(HCC)是最常见的原发性肝癌类型,也是癌症导致死亡的主要原因之一。由于该癌症缺乏有效的传统治疗选择,尤其是在晚期病例中,包括免疫治疗在内的新型治疗方法已被考虑。然而,尽管在实施这些创新方法(如溶瘤病毒(OVs)、过继细胞疗法(ACT)、免疫检查点阻断(ICBs)和癌症疫苗)后取得了令人鼓舞的临床结果,但多种因素限制了其治疗效果。主要关注点是存在免疫抑制性肿瘤微环境(TME)。不同ICBs的联合或ICBs联合酪氨酸激酶抑制剂已在某种程度上显示出克服这些限制因素的有希望的结果。程序性细胞死亡配体-1(PD-L1)抗体Atezolizumab和血管内皮生长因子(VEGF)抗体Bevacizumab的联合已成为不可测试HCC一线治疗的标准治疗,并获得监管机构批准。本文重点概述了为治疗HCC患者提出的直接和间接免疫治疗策略,以及阻碍其进一步临床应用的常见挑战。

展开英文摘要原文

Hepatocellular carcinoma (HCC) is the most common type of primary hepatic cancer and is among the major causes of mortality due to cancer. Due to the lack of efficient conventional therapeutic options for this cancer, particularly in advanced cases, novel treatments including immunotherapy have been considered.

However, despite the encouraging clinical outcomes after implementing these innovative approaches, such as oncolytic viruses (OVs), adoptive cell therapies (ACT), immune checkpoint blockades (ICBs), and cancer vaccines, several factors have restricted their therapeutic effect. The main concern is the existence of an immunosuppressive tumor microenvironment (TME). Combination of different ICBs or ICBs plus tyrosine kinase inhibitors have shown promising results in overcoming these limiting factors to some extent.

Combination of programmed cell death ligand-1 (PD-L1) antibody Atezolizumab and vascular endothelial growth factor (VEGF) antibody Bevacizumab has become the standard of care in the first-line therapy for untestable HCC, approved by regulatory agencies. This paper highlighted a wide overview of the direct and indirect immunotherapeutic strategies proposed for the treatment of HCC patients and the common challenges that have hindered their further clinical applications.

论文信息

作者
Minaei N、Ramezankhani R、Tamimi A、Piryaei A、Zarrabi A、Aref AR、Mostafavi E、Vosough M
第一作者单位
Department of Regenerative Medicine, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, Academic Center for Education, Culture and Research (ACECR), Tehran, Iran; Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, Academic Center for Education, Culture and Research (ACECR), Tehran, Iran.Iran
通讯作者单位
Department of Regenerative Medicine, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, Academic Center for Education, Culture and Research (ACECR), Tehran, Iran; Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, Academic Center for Education, Culture and Research (ACECR), Tehran, Iran; Experimental Cancer Medicine, Institution for Laboratory Medicine, Karolinska Institutet and Karolinska University Hospital-Huddinge, Sweden. Electronic address: masvos@royaninstitute.org.Iran
文献类型
综述
期刊
European journal of cell biology2023 Mar
原文标识
PubMed 36584598 · DOI 10.1016/j.ejcb.2022.151284