← 返回

CAR-T 细胞治疗在神经系统疾病中应用的最新概述

英文原题:An updated overview of the application of CAR-T cell therapy in neurological diseases.

查看英文原题

An updated overview of the application of CAR-T cell therapy in neurological diseases.

PubMed 2023/05/17(内容时间) Biotechnol Prog Q3 · IF 2.8(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

基因修饰免疫细胞,尤其是CAR-T 细胞,在过去10年中引起了科学家的关注。在抗击癌症方面,这些细胞具有特殊的地位。血液系统恶性肿瘤、自身免疫性疾病和癌症的治疗必须包括CAR-T 细胞疗法。确定治疗靶点、副作用以及CAR-T 细胞在神经系统疾病(包括癌症和神经退行性疾病)中的应用是本研究的 goal。由于基因工程的进步,CAR-T 细胞在治疗某些神经系统疾病中已变得至关重要。由于其能够穿过血脑屏障并使用多种靶点,CAR-T 细胞在治疗神经系统癌症如胶质母细胞瘤和神经母细胞瘤方面已显示出积极作用。然而,针对MS疾病的CAR-T 细胞疗法正在研究中,可能是一种潜在的治疗选择。本研究旨在获取CAR-T 细胞在神经系统疾病和/或障碍领域的最新研究和科学文章。

展开英文摘要原文

Genetically modified immune cells, especially CAR-T cells, have captured the attention of scientists over the past 10 years. In the fight against cancer, these cells have a special place. Treatment for hematological cancers, autoimmune disorders, and cancers must include CAR-T cell therapy. Determining the therapeutic targets, side effects, and use of CAR-T cells in neurological disorders, including cancer and neurodegenerative diseases, is the goal of this study.

Due to advancements in genetic engineering, CAR-T cells have become crucial in treating some neurological disorders. CAR-T cells have demonstrated a positive role in treating neurological cancers like Glioblastoma and Neuroblastoma due to their ability to cross the blood-brain barrier and use diverse targets.

However, CAR-T cell therapy for MS diseases is being researched and could be a potential treatment option.

This study aimed to access the most recent studies and scientific articles in the field of CAR-T cells in neurological diseases and/or disorders.

论文信息

作者
Shahabifard H、Zarei M、Kookli K、Esmalian Afyouni N、Soltani N、Maghsoodi S、Adili A、Mahmoudi J
第一作者单位
Neurosciences Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.Iran
通讯作者单位
Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.Iran
文献类型
综述
期刊
Biotechnology progress2023 Sep-Oct
原文标识
PubMed 37198722 · DOI 10.1002/btpr.3356