BioprintingCellular AgricultureDrug Discovery & DevelopmentHollandMedical AMMedical Research

Researchers 3D print tumors to advance cancer immunotherapy

Leiden University is monitoring real-time interactions of these tumors with immune cells during tests

Stay up to date with everything that is happening in the wonderful world of AM via our LinkedIn community.

According to Leiden University, researchers at the Leiden Academic Centre for Drug Research have developed a groundbreaking model to advance cancer immunotherapy using a 3D printer to create mini-tumors within an environment that closely mimics human tissue. They have also developed a method to monitor real-time interactions of these tumors with immune cells during tests.

“We use this method to test enhanced T-cells and bispecific antibodies for their effectiveness,” said Anita Liao, a PhD candidate at the university. “This ensures that only the most promising candidates move forward for further research and clinical development.”

Immunotherapy

Cancer cells are adept at evading detection – using various strategies to hide from the immune system and even repel attacks. Immunotherapy aids the immune system in recognizing, attacking, and ultimately destroying cancer cells. This can be achieved by strengthening the immune system with drugs – making cancer cells more detectable – or by artificially enhancing T-cells. The Leiden University research focuses on innovative testing strategies for the latter two approaches.

Leiden University researchers 3D print tumors to advance cancer immunotherapy -  monitoring real-time interactions with immune cells.
Image credit: Liao et al. (2024).

T-cells are specialized immune cells that can attack cancer cells – with receptors on their surface that act like antennas to identify the cancer cells. By isolating a patient’s T-cells, engineering them with better antennas, and transfusing them back into the blood, T-cells can be engineered to recognize and attack cancer cells more effectively. Bispecific antibodies antibodies bind to T-cells with one arm and to cancer cells with the other – helping T-cells locate and destroy cancer cells.

Traditionally, new immunotherapies are tested by culturing tumor cells, T-cells, and sometimes antibodies together in a petri dish and observing their interactions. However, this method does not accurately reflect the complexity of the human body. “In a petri dish, T-cells grow among tumor cells and can immediately start killing them,” said Erik Danen, Professor of Cancer Drug Target Discovery. “In reality, T-cells must navigate to the tumor first, which adds complexity.”

Real-time monitoring of 3D printed tumors

The researchers have developed a more realistic model using 3D printed tumours embedded in a collagen gel. “This gel mimics human tissue. We use a 3D bioprinter with a special needle to inject tumor cells into the gel – creating small, three-dimensional tumors. They grow and invade the gel and closely resemble real tumors in the body. Next, T-cells are added that have to find their way to the tumor. The method is high-throughput and suitable for testing enhanced T-cells and antibodies,” said Anita Liao.

Leiden University researchers 3D print tumors to advance cancer immunotherapy -  monitoring real-time interactions with immune cells.
A tumor to which inactive (left) and active (right) antibodies have been added. Green indicates T-cell recruitment, red indicates tumor killing. Image credit: Liao et al. (2024).

Additionally, the team has created a system to monitor these 3D printed tumors in real-time using automated microscopes – allowing them to observe what happens inside and around the tumor and follow the immune cells. We can see not only if and how enhanced T-cells and antibodies work but also investigate the defensive strategies employed by tumor cells,” said Erik Danen.

Effectiveness

The new method has already proven successful in testing various bispecific antibodies. The researchers found that not all antibodies were effective – contrary to what older models suggested. “In the new, more complex model, we observed that the most effective antibodies not only activate T-cells but also trigger the production of signaling molecules that attract additional T-cells. With the old method, the antibodies did not have a chance to reveal this behavior, because T-cells were mixed with tumor cells and could begin killing them immediately. Our new method will help identify the most effective antibodies for further clinical development,” said Erik Danen.

New treatments for breast and eye cancer

The team already uses their model to test improved T-cell receptors. For instance, they are evaluating receptors developed by immunologist Mirjam Heemskerk from Leiden University Medical Center for eye cancer treatment. They have also collaborated with Reno Debets’ immunology lab at Erasmus Medical Center in Rotterdam to test new receptors for breast cancer therapy. “Our model has successfully predicted which receptors will be effective in mouse models,” said Erik Danen. “These enhanced receptors are now ready for clinical trials in real patients. We hope our research represents a significant step forward in selecting optimal treatment for cancer patients.”

Related Articles

Leave a Reply

Your email address will not be published. Required fields are marked *

Back to top button