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嵌合抗原受体 T 细胞在临床前胶质母细胞瘤模型中的多模态体内追踪。

Multimodal In Vivo Tracking of Chimeric Antigen Receptor T Cells in Preclinical Glioblastoma Models.

机构信息

From the Molecular Imaging Program at Stanford, Department of Radiology, School of Medicine.

Lillian S. Wells Department of Neurosurgery, University of Florida, Gainesville.

出版信息

Invest Radiol. 2023 Jun 1;58(6):388-395. doi: 10.1097/RLI.0000000000000946. Epub 2022 Dec 21.

Abstract

OBJECTIVES

Iron oxide nanoparticles have been used to track the accumulation of chimeric antigen receptor (CAR) T cells with magnetic resonance imaging (MRI). However, the only nanoparticle available for clinical applications to date, ferumoxytol, has caused rare but severe anaphylactic reactions. MegaPro nanoparticles (MegaPro-NPs) provide an improved safety profile. We evaluated whether MegaPro-NPs can be applied for in vivo tracking of CAR T cells in a mouse model of glioblastoma multiforme.

MATERIALS AND METHODS

We labeled tumor-targeted CD70CAR (8R-70CAR) T cells and non-tumor-targeted controls with MegaPro-NPs, followed by inductively coupled plasma optical emission spectroscopy, Prussian blue staining, and cell viability assays. Next, we treated 42 NRG mice bearing U87-MG/eGFP-fLuc glioblastoma multiforme xenografts with MegaPro-NP-labeled/unlabeled CAR T cells or labeled untargeted T cells and performed serial MRI, magnetic particle imaging, and histology studies. The Kruskal-Wallis test was conducted to evaluate overall group differences, and the Mann-Whitney U test was applied to compare the pairs of groups.

RESULTS

MegaPro-NP-labeled CAR T cells demonstrated significantly increased iron uptake compared with unlabeled controls ( P < 0.01). Cell viability, activation, and exhaustion markers were not significantly different between the 2 groups ( P > 0.05). In vivo, tumor T2* relaxation times were significantly lower after treatment with MegaPro-NP-labeled CAR T cells compared with untargeted T cells ( P < 0.01). There is no significant difference in tumor growth inhibition between mice injected with labeled and unlabeled CAR T cells.

CONCLUSIONS

MegaPro-NPs can be used for in vivo tracking of CAR T cells. Because MegaPro-NPs recently completed phase II clinical trial investigation as an MRI contrast agent, MegaPro-NP is expected to be applied to track CAR T cells in cancer immunotherapy trials in the near future.

摘要

目的

氧化铁纳米颗粒已被用于通过磁共振成像(MRI)追踪嵌合抗原受体(CAR)T 细胞的积累。然而,迄今为止,唯一可用于临床应用的纳米颗粒 Ferumoxytol 已引起罕见但严重的过敏反应。MegaPro 纳米颗粒(MegaPro-NPs)提供了更好的安全性。我们评估了 MegaPro-NPs 是否可用于在多形性胶质母细胞瘤的小鼠模型中对 CAR T 细胞进行体内追踪。

材料和方法

我们用 MegaPro-NPs 标记靶向肿瘤的 CD70CAR(8R-70CAR)T 细胞和非靶向肿瘤对照细胞,然后进行电感耦合等离子体发射光谱、普鲁士蓝染色和细胞活力测定。接下来,我们用 MegaPro-NP 标记/未标记的 CAR T 细胞或标记的非靶向 T 细胞治疗 42 只携带 U87-MG/eGFP-fLuc 胶质母细胞瘤异种移植物的 NRG 小鼠,并进行连续 MRI、磁粒子成像和组织学研究。Kruskal-Wallis 检验用于评估总体组间差异,Mann-Whitney U 检验用于比较各组间差异。

结果

与未标记对照相比,MegaPro-NP 标记的 CAR T 细胞表现出明显增加的铁摄取(P < 0.01)。两组间细胞活力、激活和耗竭标志物无显著差异(P > 0.05)。在体内,与未靶向 T 细胞相比,用 MegaPro-NP 标记的 CAR T 细胞治疗后肿瘤 T2*弛豫时间明显降低(P < 0.01)。注射标记和未标记的 CAR T 细胞的小鼠之间的肿瘤生长抑制没有显著差异。

结论

MegaPro-NPs 可用于 CAR T 细胞的体内追踪。由于 MegaPro-NPs 最近完成了作为 MRI 造影剂的 II 期临床试验研究,预计在不久的将来,MegaPro-NP 将被应用于癌症免疫治疗试验中追踪 CAR T 细胞。

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In vivo imaging of nanoparticle-labeled CAR T cells.体内纳米颗粒标记的 CAR T 细胞成像。
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