Immune Cells Turn into Cancer Therapies Inside Tumors
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KAIST Researchers Develop novel Immunotherapy to Reprogram tumor Macrophages for Cancer Treatment
– Korea advanced Institute of Science and Technology
Researchers at the Korea advanced Institute of Science and Technology (KAIST) have developed a new immunotherapy approach that directly converts immune cells within tumors – specifically macrophages – into effective anticancer therapies. this breakthrough addresses a key challenge in cancer treatment: the suppression of immune cells by the tumor microenvironment.
Tumors often contain macrophages, immune cells with the potential to fight cancer. However, these cells are frequently suppressed by the tumor, hindering their ability to function effectively. The KAIST team, led by Professor Ji-Ho Park of the Department of Biotechnology and Brain Engineering, has devised a method to overcome this limitation.
The therapy involves injecting a drug directly into the tumor. This drug is then absorbed by the macrophages already present within the tumor. Once inside the macrophages, the drug triggers the production of CAR (Chimeric Antigen Receptor) proteins. These CAR proteins enable the macrophages to recognize and destroy cancer cells.
CAR-Macrophage Therapy: A Novel Approach
CAR-T cell therapy, a well-established immunotherapy, involves genetically engineering a patient’s T cells to express CAR proteins. Though, CAR-T cell therapy can be associated with significant side effects. The KAIST approach offers a potential advantage by utilizing macrophages, which are naturally present in the tumor microenvironment and generally considered less toxic than T cells.
“Our research demonstrates the feasibility of converting existing immune cells within the tumor into potent anticancer agents,” explained Jun-Hee Han, Ph.D., the frist author of the study and a researcher in the Department of Biotechnology and Brain Engineering at KAIST. “This approach could potentially minimize the side effects associated with customary CAR-T cell therapy.”
The research team focused on enhancing both the delivery efficiency
and overcoming the immunosuppressive tumor environment
to maximize the therapeutic effect. The direct injection method ensures a high concentration of the drug reaches the target macrophages,while the reprogramming process circumvents the tumor’s suppression mechanisms.
Publication Details and Funding
The findings were published on November 18, 2023, in ACS Nano, a leading international journal in the field of nanotechnology. The research article is titled and details the methodology and results of the study.
This research was supported by the Mid-Career Research Programme of the national Research Foundation of Korea. The project underscores the importance of continued investment in basic research to drive innovation in cancer treatment.
