用MND启动子靶向CD19 CAR-T增强肿瘤杀伤

IF 4.2
Xiaomei Zhang, Xiaoyuan He, Yu Zhang, Jile Liu, Shujing Guo, Cuicui Lyu, Mingfeng Zhao
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引用次数: 0

摘要

尽管嵌合抗原受体(CAR) T细胞疗法在B细胞急性淋巴细胞白血病中显示出很高的缓解率,但对毒性和疾病复发的担忧仍然存在。不同的启动子可以调节细胞表面CAR分子的表达水平。在这项研究中,我们系统地比较了四种不同的启动子(MND, MSCV, EF-1α和CMV)。我们的研究结果表明,虽然这些启动子具有相似的特征,但MND启动子具有更好的病毒包装和转导效率。此外,它通过增加naïve T细胞参与细胞毒性过程的比例来增强抗白血病的功效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Targeting CD19 CAR-T With MND Promoter Enhances Tumour Killing

Targeting CD19 CAR-T With MND Promoter Enhances Tumour Killing

Although Chimeric antigen receptor (CAR) T cell therapy has demonstrated a high remission rate in B cell acute lymphoblastic leukaemia, concerns regarding toxicity and disease recurrence remain. Different promoters can modulate the expression levels of CAR molecules on the cell surface. In this study, we systematically compared four distinct promoters (MND, MSCV, EF-1α and CMV). Our findings revealed that while these promoters exhibited similar characteristics, the MND promoter demonstrated superior viral packaging and transduction efficiency. Furthermore, it enhanced the anti-leukaemia efficacy by increasing the proportion of naïve T cells involved in the cytotoxic process.

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来源期刊
CiteScore
11.50
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0.00%
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期刊介绍: The Journal of Cellular and Molecular Medicine serves as a bridge between physiology and cellular medicine, as well as molecular biology and molecular therapeutics. With a 20-year history, the journal adopts an interdisciplinary approach to showcase innovative discoveries. It publishes research aimed at advancing the collective understanding of the cellular and molecular mechanisms underlying diseases. The journal emphasizes translational studies that translate this knowledge into therapeutic strategies. Being fully open access, the journal is accessible to all readers.
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