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本文引用的文献

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Adoptive cell transfer as personalized immunotherapy for human cancer.过继性细胞转移作为人类癌症的个性化免疫疗法。
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Tumor-infiltrating lymphocytes genetically engineered with an inducible gene encoding interleukin-12 for the immunotherapy of metastatic melanoma.经基因工程改造的肿瘤浸润淋巴细胞,其携带可诱导的白细胞介素-12编码基因,用于转移性黑色素瘤的免疫治疗。
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Targeted cancer immunotherapy via combination of designer bispecific antibody and novel gene-engineered T cells.通过定制双特异性抗体与新型基因工程T细胞联合进行靶向癌症免疫治疗。
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Insights into cytokine-receptor interactions from cytokine engineering.细胞因子工程对细胞因子-受体相互作用的见解。
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Molecular regulation of effector and memory T cell differentiation.效应器和记忆 T 细胞分化的分子调控。
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Paradoxical signaling by a secreted molecule leads to homeostasis of cell levels.分泌分子的矛盾信号导致细胞水平的动态平衡。
Cell. 2014 Aug 28;158(5):1022-1032. doi: 10.1016/j.cell.2014.07.033.
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Sending mixed messages for cell population control.传递用于细胞群体控制的混合信号。
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Optogenetic control of chemokine receptor signal and T-cell migration.光遗传学控制趋化因子受体信号和 T 细胞迁移。
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用于改造T细胞的合成生物学方法。

Synthetic biology approaches to engineer T cells.

作者信息

Wu Chia-Yung, Rupp Levi J, Roybal Kole T, Lim Wendell A

机构信息

Dept. of Cellular & Molecular Pharmacology, University of California San Francisco, San Francisco, CA 94158, United States.

Dept. of Cellular & Molecular Pharmacology, University of California San Francisco, San Francisco, CA 94158, United States; Howard Hughes Medical Institute, University of California San Francisco, San Francisco, CA 94158, United States.

出版信息

Curr Opin Immunol. 2015 Aug;35:123-30. doi: 10.1016/j.coi.2015.06.015. Epub 2015 Jul 25.

DOI:10.1016/j.coi.2015.06.015
PMID:26218616
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4553068/
Abstract

There is rapidly growing interest in learning how to engineer immune cells, such as T lymphocytes, because of the potential of these engineered cells to be used for therapeutic applications such as the recognition and killing of cancer cells. At the same time, our knowhow and capability to logically engineer cellular behavior is growing rapidly with the development of synthetic biology. Here we describe how synthetic biology approaches are being used to rationally alter the behavior of T cells to optimize them for therapeutic functions. We also describe future developments that will be important in order to construct safe and precise T cell therapeutics.

摘要

由于工程化免疫细胞(如T淋巴细胞)在识别和杀伤癌细胞等治疗应用方面的潜力,人们对学习如何构建这类细胞的兴趣正迅速增长。与此同时,随着合成生物学的发展,我们在逻辑上设计细胞行为的技术和能力也在迅速提高。在此,我们描述了如何利用合成生物学方法合理改变T细胞的行为,以优化其治疗功能。我们还阐述了构建安全、精准的T细胞疗法未来所需的重要进展。