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多用途 CAR:相同引擎,不同载体

英文原题:Multipurposing CARs: Same engine, different vehicles.

查看英文原题

Multipurposing CARs: Same engine, different vehicles.

PubMed 2022/02/11(内容时间) Mol Ther Q1 · IF 11.4(JCR 2025)

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中文摘要

过去十年中,通过合成嵌合抗原受体(CAR)进行基因工程改造以识别和消除肿瘤细胞的T细胞,在治疗B细胞白血病方面已展现出显著的临床疗效。该疗法是一种高度个性化的医学形式,涉及对患者T细胞进行基因修饰,使其能够识别并杀死癌细胞。随着FDA批准了5种CAR-T 细胞产品,该方法已被验证为抗癌治疗武器库中一种强大的新药。研究人员目前正在研究如何将该技术从传统多克隆T细胞的应用扩展到其他领域,以解决当前癌症治疗中的局限性及其在癌症之外的应用。考虑到来自不同谱系的免疫细胞具有特定特征,多项临床前和临床研究正在进行中,以评估在这些细胞中通过CAR重定向功能的优势,并将从癌症CAR-T 细胞疗法中获得的经验应用于其他疾病。

展开英文摘要原文

T cells genetically engineered to recognize and eliminate tumor cells through synthetic chimeric antigen receptors (CARs) have demonstrated remarkable clinical efficacy against B cell leukemia over the past decade. This therapy is a form of highly personalized medicine that involves genetically modifying a patient's T cells to recognize and kill cancer cells. With the FDA approval of 5 CAR T cell products, this approach has been validated as a powerful new drug in the therapeutic armamentarium against cancer.

Researchers are now studying how to expand this technology beyond its use in conventional polyclonal T cells to address limitations to the current therapy in cancer and applications beyond it. Considering the specific characteristics of immune cell from diverse lineages, several preclinical and clinical studies are under way to assess the advantages of CAR-redirected function in these cells and apply the lessons learned from CAR T cell therapy in cancer to other diseases.

论文信息

作者
Hossian AKMN、Hackett CS、Brentjens RJ、Rafiq S
第一作者单位
Department of Hematology and Medical Oncology, Emory University, Atlanta, GA 30322, USA.United States
通讯作者单位
Department of Hematology and Medical Oncology, Emory University, Atlanta, GA 30322, USA; Winship Cancer Institute, Emory University, Atlanta, GA 30322, USA. Electronic address: sarwish.rafiq@emory.edu.United States
文献类型
综述 · 美国 NIH 资助研究 · 非美国政府资助研究
期刊
Molecular therapy : the journal of the American Society of Gene Therapy2022 Apr 6
原文标识
PubMed 35151842 · DOI 10.1016/j.ymthe.2022.02.012