为肝细胞癌武装 GPC3 CAR T 细胞:多少才足够,下一步是什么?
Armouring GPC3 CAR T cells for hepatocellular carcinoma: how much is enough and what comes next?
英文原题:Progress and challenges in glypican-3 targeting for hepatocellular carcinoma therapy.
GPC3 是 HCC 免疫治疗的理想肿瘤抗原。
引言:Glypican-3(GPC3)是一种锚定于细胞膜的硫酸乙酰肝素蛋白聚糖,近期因其在多种癌症、尤其是肝细胞癌(HCC)中高表达且在成人正常组织中表达有限而成为关注的癌症抗原。综述范围:我们基于使用 GPC3 肽疫苗治疗 HCC 的经验,阐述 GPC3 作为癌症抗原的潜力;该疫苗已从临床前研究推进至首次人体临床试验。本综述聚焦临床试验,总结靶向 GPC3 免疫疗法的现状和未来前景,包括肽疫苗、mRNA 疫苗、抗体疗法和嵌合抗原受体/ T 细胞受体工程化 T 细胞疗法,并讨论通过免疫治疗有效清除 HCC 的其他策略。专家观点:GPC3 是 HCC 免疫治疗的理想癌症抗原。对于可切除 HCC,利用生理性免疫监视、免疫检查点抑制剂和 GPC3 靶向癌症疫苗的免疫疗法有望预防复发,可考虑作为预防性辅助治疗。然而,与临床前研究相比,晚期 HCC 临床试验尚未显示足够抗肿瘤疗效。逆向转化研究,即从临床回到实验室的研究,对于识别阻碍 GPC3 靶向免疫疗法的因素至关重要。
INTRODUCTION: Glypican-3 (GPC3) is a cell membrane-anchored heparan sulfate proteoglycan that has recently garnered attention as a cancer antigen owing to its high expression in numerous cancers, particularly hepatocellular carcinoma (HCC), and to limited expression in adult normal tissue. AREAS COVERED: Here, we propose the potential of GPC3 as a cancer antigen based on our experience with the GPC3 peptide vaccine against HCC, having developed a vaccine that progressed from preclinical studies to first-in-human clinical trials. In this review, we present a summary of the current status and future prospects of immunotherapies targeting GPC3 by focusing on clinical trials; peptide vaccines, mRNA vaccines, antibody therapy, and chimeric antigen receptor/T-cell receptor - T-cell therapy and discuss additional strategies for effectively eliminating HCC through immunotherapy. EXPERT OPINION: GPC3 is an ideal cancer antigen for HCC immunotherapy. In resectable HCC, immunotherapies that leverage physiological immune surveillance, immune checkpoint inhibitors, and GPC3-target cancer vaccines appear promising in preventing recurrence and could be considered as a prophylactic adjuvant therapy. However, in advanced HCC, clinical trials have not demonstrated sufficient anti-tumor efficacy, in contrast with preclinical studies. Reverse translation, bedside-to-bench research, is crucial to identify the factors that have hindered GPC3 target immunotherapies.
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