CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:A dual-luciferase bioluminescence system for the assessment of cellular therapies.
A dual-luciferase bioluminescence system for the assessment of cellular therapies.
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生物发光成像是临床前研究中评估工程化细胞疗法的成熟平台。然而,尽管发现了新的荧光素酶和底物,可同时监测两种细胞群的最佳组合仍有限,使细胞疗法的功能评估变得繁琐且昂贵,尤其是在临床前体内模型中。本研究探讨将发射绿色生物发光的叩头虫荧光素酶CBG99与发射红色生物发光的萤火虫荧光素酶突变体Akaluc结合,能否同时监测两种细胞群。通过多组CAR-T 细胞与肿瘤细胞配对,我们证明这些荧光素酶适用于体外二维和三维培养及体内实验模型,可实时追踪两种细胞类型。数据显示,该双荧光素酶(duo-luc)系统与多种生物发光检测设备广泛兼容,从台式分光光度计到活体动物成像系统均可使用。尽管本研究聚焦复杂CAR-T 细胞与肿瘤细胞相互作用,该duo-luc系统也可用于同时监测任意两种细胞成分,例如解析特定遗传变异对混合肿瘤细胞群中克隆优势的影响。
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 in vivo 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 in vitro and experimental models in vivo .
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.
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