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嵌合抗原受体T细胞和嵌合抗原受体NK细胞疗法在儿童和成人高级别胶质瘤中的应用——最新进展

Chimeric Antigen Receptor T Cell and Chimeric Antigen Receptor NK Cell Therapy in Pediatric and Adult High-Grade Glioma-Recent Advances.

作者信息

Kowalczyk Adrian, Zarychta Julia, Marszołek Anna, Zawitkowska Joanna, Lejman Monika

机构信息

Student Scientific Society of Department of Pediatric Hematology, Oncology and Transplantology, Medical University of Lublin, 20-093 Lublin, Poland.

Student Scientific Society of Independent Laboratory of Genetic Diagnostics, Medical University of Lublin, 20-093 Lublin, Poland.

出版信息

Cancers (Basel). 2024 Jan 31;16(3):623. doi: 10.3390/cancers16030623.

DOI:10.3390/cancers16030623
PMID:38339374
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10854514/
Abstract

High-grade gliomas (HGG) account for approximately 10% of central nervous system (CNS) tumors in children and 25% of CNS tumors in adults. Despite their rare occurrence, HGG are a significant clinical problem. The standard therapeutic procedure in both pediatric and adult patients with HGG is the surgical resection of the tumor combined with chemotherapy and radiotherapy. Despite intensive treatment, the 5-year overall survival in pediatric patients is below 20-30%. This rate is even lower for the most common HGG in adults (glioblastoma), at less than 5%. It is, therefore, essential to search for new therapeutic methods that can extend the survival rate. One of the therapeutic options is the use of immune cells (T lymphocytes/natural killer (NK) cells) expressing a chimeric antigen receptor (CAR). The objective of the following review is to present the latest results of preclinical and clinical studies evaluating the efficacy of CAR-T and CAR-NK cells in HGG therapy.

摘要

高级别胶质瘤(HGG)约占儿童中枢神经系统(CNS)肿瘤的10%,占成人CNS肿瘤的25%。尽管其发病率较低,但HGG仍是一个重大的临床问题。儿童和成人HGG患者的标准治疗程序是手术切除肿瘤并结合化疗和放疗。尽管进行了强化治疗,但儿童患者的5年总生存率仍低于20%-30%。对于成人中最常见的HGG(胶质母细胞瘤),这一比率甚至更低,不到5%。因此,寻找能够提高生存率的新治疗方法至关重要。治疗选择之一是使用表达嵌合抗原受体(CAR)的免疫细胞(T淋巴细胞/自然杀伤(NK)细胞)。以下综述的目的是介绍评估CAR-T和CAR-NK细胞在HGG治疗中疗效的临床前和临床研究的最新结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/768e/10854514/66e3f7b6ca0b/cancers-16-00623-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/768e/10854514/9958f1a88f27/cancers-16-00623-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/768e/10854514/6bcbfe949998/cancers-16-00623-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/768e/10854514/66e3f7b6ca0b/cancers-16-00623-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/768e/10854514/9958f1a88f27/cancers-16-00623-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/768e/10854514/6bcbfe949998/cancers-16-00623-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/768e/10854514/66e3f7b6ca0b/cancers-16-00623-g003.jpg

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结直肠癌:风险因素、分子筛查与治疗的新方法
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Strategies to overcome tumor microenvironment immunosuppressive effect on the functioning of CAR-T cells in high-grade glioma.克服肿瘤微环境对高级别胶质瘤中CAR-T细胞功能的免疫抑制作用的策略。
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