← 返回

肺癌免疫治疗:聚焦嵌合抗原受体(CAR)-T 细胞治疗

英文原题:Immunotherapy for lung cancer: Focusing on chimeric antigen receptor (CAR)-T cell therapy.

查看英文原题

Immunotherapy for lung cancer: Focusing on chimeric antigen receptor (CAR)-T cell therapy.

PubMed 2021/09/03(内容时间) Curr Probl Cancer Q3 · IF 2.4(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

除手术、放疗和化疗等传统肺癌治疗策略外,免疫疗法也已成为一种新型治疗手段。免疫疗法旨在通过治疗性疫苗、单克隆抗体、免疫检查点抑制剂和T细胞疗法等多种方式,刺激免疫系统抗癌。嵌合抗原受体(CAR)T细胞是近十年来最受关注的癌症免疫疗法之一,它通过基因工程改造T细胞,将患者的免疫应答重定向至表达肿瘤相关抗原(TAA)的肿瘤细胞,从而识别并清除肿瘤。CAR-T 细胞疗法在肺部肿瘤中显示出应用前景。本综述总结了肺癌的不同免疫治疗方法、CAR-T 细胞结构、当前进入临床试验的CAR构建体,以及正在研究用于设计肺癌CAR-T 细胞的潜在TAA靶点。

展开英文摘要原文

Besides traditional treatment strategies, including surgery, radiotherapy, and chemotherapy for lung cancer as the leading cause of cancer incidence and death, immunotherapy has also emerged as a new treatment strategy. The goal of immunotherapy is to stimulate the immune system responses against cancer, using various approaches such as therapeutic vaccines, monoclonal antibodies, immune checkpoint inhibitors, and T-cell therapy.

Chimeric antigen receptor (CAR)-T cells, one of the most popular cancer immunotherapy approaches in the last decade, are genetically engineered T-cells to redirect patients' immune responses to recognize and eliminate tumor-associated antigens (TAA)-expressing tumor cells.

CAR-T cell therapy provides promising benefits in lung tumors. In this review, we summarize different immunotherapy approaches for lung cancer, the structure of CAR-T cells, currently undergoing CARs in clinical trials, and various TAAs are being investigated as potential targets in designing CAR-T cells for lung cancer.

论文信息

作者
Xue T、Zhao X、Zhao K、Lu Y、Yao J、Ji X
第一作者单位
Department of Pain and Intervention Management, Huaian Hospital of Huaian City, Huaian 223200, Jiangsu, China.China
通讯作者单位
Department of Radiation Oncology, Huaian Hospital of Huaian City, Huaian 223200, Huaian, Jiangsu, China. Electronic address: jixianguo501@126.com.China
文献类型
综述
期刊
Current problems in cancer2022 Feb
原文标识
PubMed 34538649 · DOI 10.1016/j.currproblcancer.2021.100791