← 返回

恶性黑色素瘤的 CAR-T 细胞免疫治疗

英文原题:CAR-T cell immunotherapy of malignant melanoma.

查看英文原题

CAR-T cell immunotherapy of malignant melanoma.

PubMed 2026/02/03(内容时间) Expert Rev Clin Immunol Q2 · IF 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。

研究概要

CAR-T 细胞免疫疗法已证实在部分血液系统恶性肿瘤的治疗中具有变革性。

中文摘要

引言:近年来,免疫检查点阻断、小分子抑制剂以及离体扩增TIL(肿瘤浸润淋巴细胞)的过继免疫疗法等多种治疗方式的出现,改变了不可手术和晚期恶性黑色素瘤的管理。 综述范围:本综述介绍采用嵌合抗原受体(CAR)工程化T细胞,为该疾病开发替代免疫疗法的研究工作。我们检索了PubMed数据库和ClinicalTrials.gov网站中1998至2025年的文献。 专家观点:CAR-T 细胞免疫疗法已显著改变部分血液系统恶性肿瘤的治疗。然而,黑色素瘤等实体瘤仍远比血液瘤更难用这一新兴疗法治疗。本文探讨靶点选择问题,包括肿瘤细胞及其周围基质;还讨论可增强CAR-T 递送至肿瘤或提高其在肿瘤微环境内疗效的装甲化策略。此外,我们考察多种先进CAR架构,以实现多抗原或通用抗原靶向,并介绍联合治疗方法。

展开英文摘要原文

INTRODUCTION: Management of inoperable and advanced malignant melanoma has been transformed in recent years by the advent of a number of approaches, including immune checkpoint blockade, small-molecule inhibitors, and adoptive immunotherapy with ex vivo expanded tumor-infiltrating lymphocytes.

AREAS COVERED: In this review, we describe efforts made to develop an alternative immunotherapeutic approach for this disease using chimeric antigen receptor (CAR) engineered T-cells. Literature was reviewed in the PubMed database and clinicaltrials. gov website (1998-2025). EXPERT OPINION: CAR T-cell immunotherapy has proven transformative in the treatment of selected hematological malignancies.

However, solid tumors such as melanoma remain much more challenging to treat using this emerging modality.

Here we consider issues surrounding target selection, encompassing both tumor cells and accompanying stroma, in addition to armoring approaches that may potentiate delivery to or efficacy within the tumor microenvironment.

We also consider a number of advanced CAR-based architectures to enable multi-antigen or universal antigen targeting and combination-based approaches.

论文信息

作者
Kharasakhal O、Maher J
单位
King's College London, School of Cancer and Pharmaceutical Sciences, Guy's Hospital, London, UK.United Kingdom
文献类型
综述
期刊
Expert review of clinical immunology2026 Jan
原文标识
PubMed 41601180 · DOI 10.1080/1744666X.2026.2621811