Method Article

Circulating Glioma Model for Chimeric Antigen Receptor T-Cell Therapy Investigations

DOI:

10.3791/68881

October 17th, 2025

In This Article

Summary

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The present protocol establishes a circulating glioma model by the lateral ventricle injection to investigate the therapeutic effect of chimeric antigen receptor T-cell therapy in vivo.

Abstract

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Circulating tumor cells in cerebrospinal fluid (CSF) are a significant factor in tumor recurrence and intracranial metastasis in glioma. Many studies are attempting to identify effective strategies to target and eliminate the circulating tumor in CSF. Chimeric antigen receptor (CAR) T-cell therapy has been frequently used for various circulating tumors. However, research is limited due to the lack of a suitable circulating glioma model. Here, a circulating glioma model was developed and applied in CAR T-cell therapy investigations. This model was constructed using the lateral ventricle injection, which is widely used in the local treatment of intracranial disease. The glioma cells were injected into the lateral ventricle to form the intracranial primary tumor. The tumors that were shed from the lateral ventricle were used to indicate the circulating tumor in CSF. The model is easy to build and can be applied in various studies on the CAR T-cell therapy of circulating glioma. As a result, the circulating glioma model provides a unique glioma metastasis model for effective CAR T-cell therapy studies of the circulating tumor.

Introduction

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Glioma is the most common primary malignant brain tumor in adults1,2. Current treatments, including surgery, radiotherapy, and chemotherapy, show limited efficacy, with a median survival of only 14-15 months3,4,5. Circulating glioma cells in CSF play a crucial role in tumor recurrence and intracranial metastasis6,7. Hence, there is an urgent need to develop more effective treatment strategies to eliminate the circulating glioma cells.

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Protocol

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The animal experiments in this study were all approved and supervised by the Institutional Review Board and the Animal Ethics Committee of Nanjing Medical University (IACUC-1905048). C57BL/6J female mice, aged 6-8 weeks old, were used for the present study. The reagents and the equipment used are listed in the Table of Materials.

1. Animal preparation

  1. House the mice in a barrier, 12 h/12 h light/dark cycle, ambient temperature of 24 °C, and relative humidity of 50% cage.
  2. Weigh the mice, and anesthetize them (following institutionally approved protocols) with an intraperitoneal injection of 50 mg/k....

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Results

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The schematic diagram of the circulating glioma model for CAR-T therapy is shown in Figure 1. CAR-T cells were injected into the lateral ventricle using a microsyringe to demonstrate their therapeutic effect. This method allows direct delivery of the CAR-T cells to the brain, targeting the circulating glioma cells. The injection procedure was performed on day 11, following the implantation of GL261 cells into the mouse lateral ventricle. At various time point.......

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Discussion

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The circulating glioma model established in this study using lateral ventricle injection provides a significant advancement, offering several advantages over existing models. The lateral ventricle injection technique is highly reproducible, enabling consistent tumor modeling in a relatively short time frame. This makes it a valuable tool for researchers seeking to investigate tumor cell dissemination into the CSF and assess the effectiveness of therapies, such as CAR-T cells. Unlike traditional intravenous CAR-T infusion.......

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Disclosures

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The authors declare no conflicts of interest.

Acknowledgements

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This study was funded by the National Natural Science Foundation of China (82230059), the Jiangsu Provincial Key Research Development Program of China (BE2022770).

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
Absorbable surgical sutureShanghai Pudong Jinhuan Medical Products Co.,LtdR611
CAR-TCreative Biolabs
D-Luciferin potassium saltMCEHY-12591B
GL261-Luc-GfpShanghai Zhong Qiao Xin Zhou Biotechnology Co.,Ltd.ZQ0932
In vivo bioluminescent imaging systemTanonTanon ABL X6
Laboratory animal shaverBeyotime BiotechnologyFS600
MiceAnimal Core Facility of Nanjing Medical University
Microinjection pumpRWDR462
MicrosyringeHamilton87943
Mini cranial drillRWD78001
Pentobarbital sodium ChemSrc57-33-0
Stereotaxic apparatusRWD68043
XylazineChemSrc7361-61-7

References

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  1. Lim, M., Xia, Y., Bettegowda, C., Weller, M. Current state of immunotherapy for glioblastoma. Nat Rev Clin Oncol. 15 (7), 422-442 (2018).
  2. Weller, M., et al. Glioma. Nat Rev Dis Primers. 10 (1), 33(2024).
  3. Van Den Bent, M. J., et al.

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Tags

Circulating Glioma ModelCAR T Cell TherapyCerebrospinal Fluid TumorGlioma MetastasisLateral Ventricle InjectionIntracranial TumorTumor RecurrenceChimeric Antigen ReceptorCirculating Tumor CellsIntracranial Metastasis

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