← 返回

以抗检查点分子改造 CAR-T 细胞用于肿瘤免疫治疗:聚焦抗 PD-1/PD-L1 抗体

英文原题:Modifying CAR-T cells with anti-checkpoints in cancer immunotherapy: A focus on anti PD-1/PD-L1 antibodies.

查看英文原题

Modifying CAR-T cells with anti-checkpoints in cancer immunotherapy: A focus on anti PD-1/PD-L1 antibodies.

PubMed 2023/12/26(内容时间) Life Sci Q1 · IF 6.4(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

中文摘要

嵌合抗原受体修饰T(CAR-T)细胞是经过基因工程改造以表达肿瘤特异性抗原的细胞,正在彻底改变血液系统恶性肿瘤的治疗。对于CAR-T 细胞疗法在实体瘤中的应用,敌对的肿瘤微环境(TME)仍然是一个挑战。作为一种解决方案,与免疫检查点抑制剂(ICIs)的联合治疗已被证明可以提高CAR-T 细胞疗法的安全性和有效性。为了避免联合治疗中应用ICIs相关的副作用,工程化CAR以表达肿瘤特异性抗原可能有助于改善临床结局。那些表达针对免疫检查点刺激性或抑制性分子(如程序性死亡-1(PD-1)/程序性死亡配体1(PD-L1)信号轴)的单链可变片段(scFvs)或纳米抗体的CAR正在各种临床试验中被广泛研究。在这篇综述中,我们讨论了表达抗PD-(L)1 scFv的CAR-T 细胞在人类癌症治疗中的意义,描述了当前的挑战以及在癌症免疫治疗领域克服这些困境的潜在策略。

展开英文摘要原文

Chimeric antigen receptor-modified T (CAR-T) are genetically engineered cells to express tumor-specific antigens revolutionizing the treatment of hematologic malignancies. The hostile tumor microenvironment (TME) remains a challenge for CAR-T cell therapy in solid tumors. As a solution, combinational therapy with immune checkpoint inhibitors (ICIs) is shown to improve the safety and efficacy of CAR-T cell therapy. To avoid side effects related to the application of ICIs in combinational therapy, engineering CARs to express tumor-specific antigens may help improvement of clinical outcomes.

Those CARs expressing single chain variable fragments (scFvs) or nanobodies against immune checkpoint stimulatory or inhibitory molecules, such as the programmed death-1 (PD-1)/programmed death-ligand 1 (PD-L1) signaling axis are being extensively studied in various clinical trials. In this review, we discuss the significance of anti-PD-(L)1 scFv-expressing CAR-T cells in the treatment of human cancers, describing current challenges and potential strategies to overcome such predicaments in the area of cancer immunotherapy.

论文信息

作者
Najafi S、Mortezaee K
第一作者单位
Department of Medical Biotechnology, School of Advanced Technologies in Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran; Cellular and Molecular Biology Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.Iran
通讯作者单位
Department of Anatomy, School of Medicine, Kurdistan University of Medical Sciences, Sanandaj, Iran. Electronic address: mortezaee.k@muk.ac.ir.Iran
文献类型
综述
期刊
Life sciences2024 Feb 1
原文标识
PubMed 38154609 · DOI 10.1016/j.lfs.2023.122387