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A Nonviral Approach to Generate Transient Chimeric Antigen Receptor T Cells Using mRNA for Cancer Immunotherapy
Published on: February 21, 2025
759
CD24: A Novel Target for Cancer Immunotherapy
Emmanouil Panagiotou1, Nikolaos K Syrigos1, Andriani Charpidou1
1Section of Medical Oncology, Third Department of Internal Medicine, National and Kapodistrian University of Athens, 11527 Athens, Greece.
Journal of Personalized Medicine
|August 26, 2022
Summary
Cluster of differentiation 24 (CD24) is a cell adhesion protein. Blocking CD24 shows promise for cancer immunotherapy by overcoming tumor immune evasion and enhancing immune cell activity.
Area of Science:
- Immunology
- Oncology
- Molecular Biology
Background:
- Cluster of differentiation 24 (CD24) is a glycosylated cell adhesion protein found on immune and other cell types.
- Tumor CD24 expression correlates with oncogenic signaling pathway alterations.
- The CD24/Siglec-10 pathway is involved in tumor immune evasion, suppressing macrophage phagocytosis and natural killer (NK) cell cytotoxicity.
Purpose of the Study:
- To review current evidence on CD24 as a cancer immunotherapy target.
- To discuss future perspectives for CD24-targeted therapies.
Main Methods:
- Review of preclinical studies on CD24 blockade.
- Analysis of clinical trial data for anti-CD24 monoclonal antibodies.
- Evaluation of antibody-drug conjugates and CAR T cell therapy in preclinical settings.
Main Results:
- CD24 blockade demonstrates potential in preclinical cancer models.
- Monoclonal antibodies targeting CD24 show clinical safety and tolerability.
- Emerging therapies like antibody-drug conjugates and CAR T cells are being explored.
Conclusions:
- CD24 represents a promising target for cancer immunotherapy.
- Further research and clinical trials are warranted to optimize CD24-targeted treatment strategies.
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