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嵌合抗原受体 (CAR)-T 细胞:肝细胞癌治疗的新时代

英文原题:Chimeric Antigen Receptor (CAR)-T Cells: A New Era for Hepatocellular Carcinoma Treatment.

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Chimeric Antigen Receptor (CAR)-T Cells: A New Era for Hepatocellular Carcinoma Treatment.

PubMed 2024/12/01(内容时间) J Biochem Mol Toxicol Q2 · IF 3.6(JCR 2025)

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中文摘要

肝细胞癌(HCC)是常见癌症之一,也是全球性健康问题,需要新的治疗方法。目前标准治疗为酪氨酸激酶抑制剂(TKI)和免疫检查点阻断(ICB),但部分晚期和转移性患者的临床获益有限。近期,基因工程技术促进一种新型过继细胞疗法(ACT)——嵌合抗原受体(CAR)T细胞——用于治疗HCC。大量临床和临床前研究正尝试通过应对HCC免疫抑制环境并寻找最佳肿瘤特异性抗原(TSA),提高CAR-T 细胞疗效。新型治疗方法与ACT研究持续进展相结合,未来可能大幅改善HCC患者照护。然而,CAR-T 细胞在实体瘤中的临床应用仍面临若干挑战。本研究概述CAR-T 细胞免疫疗法治疗HCC的进展和前景,并探讨前沿工程技术如何改善CAR-T 细胞疗效和安全性。

展开英文摘要原文

Hepatocellular carcinoma (HCC) is one of the most common cancers and a worldwide health concern that requires novel treatment approaches. Tyrosine kinase inhibitors (TKIs) and immune checkpoint blockades (ICBs) are the current standard of care; however, their clinical benefits are limited in some advanced and metastatic patients. With the help of gene engineering techniques, a novel adoptive cellular therapy (ACT) called chimeric antigen receptor (CAR)-T cells was recently introduced for treating HCC.

A plethora of current clinical and preclinical studies are attempting to improve the efficacy of CAR-T cells by dominating the immunosuppressive environment of HCC and finding the best tumor-specific antigens (TSAs). The future of care for HCC patients might be drastically improved due to the convergence of novel therapeutic methods and the continuous progress in ACT research.

However, the clinical application of CAR-T cells in solid tumors is still facing several challenges. In this study, we provide an overview of the advancement and prospects of CAR-T cell immunotherapy in HCC, as well as an investigation of how cutting-edge engineering could improve CAR-T cell efficacy and safety profile.

论文信息

作者
Xu M、Pan Y
单位
Department of Liver, Gallbladder, Spleen and Stomach, Heilongjiang Academy of Chinese Mediceal Sciences, Harbin, Heilongjiang, China.China
文献类型
综述
期刊
Journal of biochemical and molecular toxicology2024 Dec
原文标识
PubMed 39664011 · DOI 10.1002/jbt.70091