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CAR-T 细胞治疗在胆管癌、胰腺癌和胃癌中的进展

英文原题:Advances in CAR T-cell therapy in bile duct, pancreatic, and gastric cancers.

查看英文原题

Advances in CAR T-cell therapy in bile duct, pancreatic, and gastric cancers.

PubMed 2022/10/06(内容时间) Front Immunol Q1 · IF 7(JCR 2025)

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中文摘要

胆管癌、胰腺癌和胃癌是恶性程度高、预后差的致命性消化系统肿瘤。传统手术、放疗和化疗的疗效有限。相比之下,嵌合抗原受体(CAR)T细胞治疗是抗肿瘤免疫的重要突破,在多种血液系统恶性肿瘤中疗效显著。CAR-T 疗法通过基因工程使患者T细胞表达特异性抗体,并扩增这些细胞,以识别和靶向肿瘤相关抗原。CAR-T 治疗可有效抑制胆管癌、胰腺癌和胃癌进展并改善患者生存。使用异种移植模型可验证CAR-T 治疗肿瘤的效果,为科学评估提供平台。本研究综述CAR-T 细胞的制备和研发进展,重点介绍其治疗胆管癌、胰腺癌和胃癌的现状及工程化优化策略。

展开英文摘要原文

Bile duct, pancreatic, and gastric cancers are deadly digestive system tumors with high malignancy and poor patient prognosis. The efficiencies of conventional surgical treatment, radiation therapy, and chemotherapy are limited. In contrast, chimeric antigen receptor (CAR) T-cell therapy represents a landmark therapeutic approach to antitumor immunity with great efficacy in treating several hematological malignancies. CAR T-cell therapy involves genetically engineering the expression of specific antibodies based on the patient's T-cell surface and amplifying these antibodies to identify and target tumor-associated antigens.

CAR T-cell therapy can effectively inhibit disease progression and improve the survival of patients with bile duct, pancreatic, and gastric cancers. The effectiveness of CAR T cells in tumor therapy can be validated using xenograft models, providing a scientific testing platform. In this study, we have reviewed the progress in CAR T-cell production and its development, focusing on the current status and optimization strategies for engineered CAR T cells in the bile duct, pancreatic, and gastric cancers.

论文信息

作者
Feng Q、Sun B、Xue T、Li R、Lin C、Gao Y、Sun L、Zhuo Y
第一作者单位
Department of Hepatobiliary and Pancreas Surgery, China - Japan Union Hospital of Jilin University, Changchun, China.China
通讯作者单位
Laboratory Animal Center, College of Animal Science, Jilin University, Changchun, China.China
文献类型
综述 · 非美国政府资助研究
期刊
Frontiers in immunology2022
原文标识
PubMed 36341440 · DOI 10.3389/fimmu.2022.1025608