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一种用于评估细胞疗法的双荧光素酶生物发光系统。

A dual-luciferase bioluminescence system for the assessment of cellular therapies.

作者信息

Torres Chavez Alejandro G, McKenna Mary K, Balasubramanian Kishore, Riffle Lisa, Patel Nimit L, Kalen Joseph D, St Croix Brad, Leen Ann M, Bajgain Pradip

机构信息

Center for Cell and Gene Therapy, Baylor College of Medicine, Houston, TX 77030, USA.

Texas A&M Health Science Center School of Medicine, Bryan, TX 77807, USA.

出版信息

Mol Ther Oncol. 2024 Jan 10;32(1):200763. doi: 10.1016/j.omton.2024.200763. eCollection 2024 Mar 21.

DOI:10.1016/j.omton.2024.200763
PMID:38596291
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10869576/
Abstract

Bioluminescence imaging is a well-established platform for evaluating engineered cell therapies in preclinical studies. However, despite the discovery of new luciferases and substrates, optimal combinations to simultaneously monitor two cell populations remain limited. This makes the functional assessment of cellular therapies cumbersome and expensive, especially in preclinical models. In this study, we explored the potential of using a green bioluminescence-emitting click beetle luciferase, CBG99, and a red bioluminescence-emitting firefly luciferase mutant, Akaluc, together to simultaneously monitor two cell populations. Using various chimeric antigen receptor T cells and tumor pairings, we demonstrate that these luciferases are suitable for real-time tracking of two cell types using 2D and 3D cultures and experimental models . Our data show the broad compatibility of this dual-luciferase (duo-luc) system with multiple bioluminescence detection equipment ranging from benchtop spectrophotometers to live animal imaging systems. Although this study focused on investigating complex CAR T cells and tumor cell interactions, this duo-luc system has potential utility for the simultaneous monitoring of any two cellular components-for example, to unravel the impact of a specific genetic variant on clonal dominance in a mixed population of tumor cells.

摘要

生物发光成像在临床前研究中是一个成熟的评估工程细胞疗法的平台。然而,尽管发现了新的荧光素酶和底物,但同时监测两个细胞群体的最佳组合仍然有限。这使得细胞疗法的功能评估既麻烦又昂贵,尤其是在临床前模型中。在本研究中,我们探索了使用绿色生物发光的叩头虫荧光素酶CBG99和红色生物发光的萤火虫荧光素酶突变体Akaluc一起同时监测两个细胞群体的潜力。通过使用各种嵌合抗原受体T细胞和肿瘤配对,我们证明这些荧光素酶适用于使用二维和三维培养物以及实验模型实时跟踪两种细胞类型。我们的数据表明,这种双荧光素酶(双luc)系统与从台式分光光度计到活体动物成像系统的多种生物发光检测设备具有广泛的兼容性。尽管本研究重点关注复杂的嵌合抗原受体T细胞与肿瘤细胞的相互作用,但这种双luc系统有潜力用于同时监测任何两个细胞成分,例如,揭示特定基因变异对肿瘤细胞混合群体中克隆优势的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71b9/10869576/c1c850b28faf/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71b9/10869576/100410e09354/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71b9/10869576/f2c72113bfe3/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71b9/10869576/0ce5ee14d0b3/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71b9/10869576/f4e36639807d/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71b9/10869576/c1c850b28faf/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71b9/10869576/100410e09354/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71b9/10869576/f2c72113bfe3/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71b9/10869576/0ce5ee14d0b3/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71b9/10869576/f4e36639807d/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71b9/10869576/c1c850b28faf/gr4.jpg

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JCO Oncol Pract. 2023 Sep;19(9):706-713. doi: 10.1200/OP.22.00819. Epub 2023 Jul 5.
2
Safety and efficacy of co-administration of CD19 and CD22 CAR-T cells in children with B-ALL relapse after CD19 CAR-T therapy.CD19 嵌合抗原受体 T 细胞治疗后复发的儿童 B 细胞急性淋巴细胞白血病中 CD19 和 CD22 嵌合抗原受体 T 细胞联合给药的安全性和有效性。
J Transl Med. 2023 Mar 22;21(1):213. doi: 10.1186/s12967-023-04019-4.
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Cancer Immunol Res. 2022 Nov 2;10(11):1370-1385. doi: 10.1158/2326-6066.CIR-22-0115.
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CAR-T cell therapy for patients with hematological malignancies. A systematic review.嵌合抗原受体 T 细胞疗法治疗血液系统恶性肿瘤。系统评价。
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