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JoVE Journal
Cancer Research
Intracranial Cannula Implantation for Serial Locoregional Chimeric Antigen Receptor (CAR) T Cell ...
Intracranial Cannula Implantation for Serial Locoregional Chimeric Antigen Receptor (CAR) T Cell ...
JoVE Journal
Cancer Research
This content is Free Access.
JoVE Journal Cancer Research
Intracranial Cannula Implantation for Serial Locoregional Chimeric Antigen Receptor (CAR) T Cell Infusions in Mice

Intracranial Cannula Implantation for Serial Locoregional Chimeric Antigen Receptor (CAR) T Cell Infusions in Mice

Full Text
4,364 Views
05:22 min
February 24, 2023

DOI: 10.3791/64886-v

Kyra Harvey1, Peter J. Madsen2,3, Tiffany Smith2, Crystal Griffin1,2, Luke Patterson1,2, Nicholas A. Vitanza4,5, Phillip B. Storm2,3, Adam C. Resnick2,3, Jessica B. Foster1,2

1Division of Oncology,Children’s Hospital of Philadelphia, 2Center for Data Driven Discovery in Biomedicine,Children’s Hospital of Philadelphia, 3Division of Neurosurgery,Children’s Hospital of Philadelphia, 4Ben Towne Center for Childhood Cancer Research,Seattle Children’s Research Institute, 5Department of Pediatrics, Seattle Children’s Hospital,University of Washington

Overview

This protocol outlines a method for locoregional cannula implantation in mice, facilitating the preclinical evaluation of immunotherapeutic infusions targeting central nervous system tumors. The technique allows for repeated doses of CAR T-cell therapy without the need for multiple invasive surgeries.

Key Study Components

Area of Science

  • Neuroscience
  • Oncology
  • Immunotherapy

Background

  • CNS tumors are the leading cause of cancer-related deaths in children.
  • Locoregional immune-based therapies are being tested in clinical trials.
  • CAR T-cell therapy shows promise in targeting CNS tumors.
  • This protocol replicates an intraventricular catheter system used in ongoing clinical trials.

Purpose of Study

  • To evaluate the effectiveness of CAR T-cell therapy in a preclinical model.
  • To provide a method for local regional delivery of therapeutics.
  • To minimize the invasiveness of repeated treatments in animal models.

Methods Used

  • Implantation of a cannula using a stereotactic apparatus.
  • Administration of CAR T-cell therapy through the implanted cannula.
  • Use of anesthesia and surgical techniques to ensure animal welfare.
  • Monitoring of tumor response and survival outcomes post-treatment.

Main Results

  • The GPC2-directed CAR T-cell therapy induced significant tumor regression.
  • Significantly prolonged survival was observed in the thalamic diffuse midline glioma model.
  • The method allows for precise delivery of treatment to targeted areas.
  • Insights gained may inform future research in neuroscience and oncology.

Conclusions

  • This protocol provides a valuable tool for studying CNS tumors.
  • It enhances the understanding of CAR T-cell therapy efficacy.
  • The approach may lead to improved therapeutic strategies for CNS tumors.

Frequently Asked Questions

What is the main advantage of this cannula implantation technique?
The main advantage is the ability to provide multiple doses of therapy without repeated invasive surgeries.
How does CAR T-cell therapy work?
CAR T-cell therapy involves engineering T-cells to target and destroy cancer cells.
What types of tumors are targeted in this study?
The study focuses on central nervous system tumors, particularly medulloblastoma and diffuse midline glioma.
What are the implications of this research?
The research may lead to improved treatment options and understanding of CNS tumors in pediatric patients.
What is the role of anesthesia in this protocol?
Anesthesia is used to ensure the welfare of the mice during the surgical procedures.
How is the effectiveness of the treatment measured?
Effectiveness is measured by tumor regression and survival rates in the treated mice.

Central nervous system (CNS) tumors are the leading cause of cancer-related death in children, and locoregional immune-based therapies are increasingly being tested for patients in clinical trials. This protocol describes methods for locoregional cannula implantation in mice for the preclinical evaluation of immunotherapeutic infusions targeting CNS tumors.

This protocol replicates an intraventricular catheter system used in ongoing clinical trials to test local regional delivery of CAR T-cell therapy directed against central nervous system tumors. The main advantage of this technique is the ability to provide multiple repeated doses of local regional CAR T-cell therapy without performing multiple invasive surgical procedures. This system could be used to investigate different therapeutics in different delivery sites, and thus may provide insight into a myriad of research areas in neuroscience.

To begin, place the anesthetized mouse with shaved head on the operation table and gently open the bottom of the stereotactic arm using a spatula. Insert the cannula with forceps and secure it by tightening the screw on the arm until half to two-thirds of the white plastic portion and five millimeters of the cannula protrude from the bottom of the opening. Insert and secure the mouse's top teeth in the bite bar of the stereotaxic apparatus.

Pull the nose cone forward and tighten it, ensuring the mouse inhales isoflurane. Then, mount the mouse on the warmed stereotaxic apparatus using ear cuffs or ear bars, avoiding excessive pressure. Disinfect the surgical site and make a cut parallel to the skull as described in the manuscript.

Use cotton tip swabs to push the fascia away. Identify the landmarks, bregma and lambda on the skull corresponding to anterior and posterior marks where the cranial plates meet. To create a surface for attaching the acrylic, gently make several slits across the skull using a scalpel.

Using the stereotaxic arm, localize the cannula to the landmark of interest. Raise the cannula tip one to two millimeters above the skull surface and move to the desired coordinates. Using an 18 gauge needle or surgical drill, make two screw holes on the exposed skull away from where the cannula enters, ensuring enough space for the cannula.

Twist the drill through the screw hole until it attaches to the skull. With a flat tip screwdriver, insert and fasten two screws into the holes. Then, gently pull the screw up to ensure it is secured.

For inserting a cannula, create a hole in the skull at the identified coordinates using an 18 gauge needle or surgical drill. Using the stereotactic arm, lower the cannula to the desired DV coordinate. At approximately 0.3 grams of acrylic resin powder and 10 to 15 drops of liquid in a porcelain 12-well plate, load the prepared viscous white-colored material into a one-milliliter syringe.

Coat the skull and fill the spaces around the cannula and screw. Loosen the screw on the stereotactic arm while the cement is flexible. Gently use a spatula to release the cannula from the holder at the bottom opening and retract the stereotactic arm away from the mouse.

Once the cement is dried, insert the dummy cannula into the guide cannula and rotate clockwise to secure it tightly. Once the procedure is complete, return the mouse to its warmed home cage for recovery. To prepare the treatment cannula, insert its top into PKG tubing.

Then, fill the treatment syringe with CAR T-cell suspension and insert it through the other end of the PKG tube, covering the top of the treatment cannula. After anesthetizing the mouse, fix the guide cannula at the base using forceps. Unscrew and remove the dummy cannula, allowing access to the guide cannula.

Infuse the CAR T-cells for one minute and hold the treatment cannula in place for an additional minute. After removing the treatment cannula, screw back a dummy cannula tightly. Then, administer meloxicam subcutaneously for pain control.

The GPC2-directed CAR T-cell therapy induced significant tumor regression in the medulloblastoma and significantly prolonged survival in the thalamic diffuse midline glioma model. When inserting the guide cannula into an intratumoral location, it's important to understand that the dorsal-ventral coordinates may be more superficial than tumor injection in order to account for the dummy and treatment cannula projection lengths.

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Intracranial CannulaCAR T-cell TherapyLocoregional DeliveryCentral Nervous System TumorsSurgical ProcedureStereotactic ApparatusAnesthetized MouseCannula InsertionSurgical DrillSkull LandmarksAcrylic AttachmentNeuroscience ResearchMultiple DosesInvasive Techniques

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