The innovation at hand is a groundbreaking advancement in the field of hematologic malignancy treatment, specifically focusing on acute lymphoblastic leukemia (ALL) in children. It involves the development of genetically modified T-cell lymphocytes expressing chimeric antigen receptors (CARs) that target CD19, a protein expressed on cancer cells. By utilizing a modified receptor and a novel spacer region, the CAR-CD19 T-cells aim to enhance specificity and function, potentially reducing the need for intensive chemotherapy and stem cell transplantation.
● Genetically modified T-cell lymphocytes expressing chimeric antigen receptors (CARs)
● CAR-CD19 T-cells designed to target CD19 protein expressed on cancer cells
● Modified receptor and novel spacer region utilizing the CH3 domain of Immunoglobulin G2 (IgG2)
● Enhanced specificity and functionality of the CAR-CD19 receptor
● Treatment of acute lymphoblastic leukemia (ALL) in children
● Management of relapsed cases of ALL through cellular therapy
● Potential application in other B-cell hematologic malignancies expressing CD19 protein
● Alternative treatment option to minimize the use of intensive chemotherapy
Current market trends indicate a growing demand for alternative treatments in hematologic malignancies, particularly those that minimize the use of chemotherapy. The development of cellular therapies utilizing genetically modified T-cells and chimeric antigen receptors (CARs) presents a significant opportunity to transform the treatment landscape for diseases like acute lymphoblastic leukemia (ALL). The market is receptive to innovative approaches that enhance specificity and functionality, offering potential benefits in terms of treatment outcomes and reduced side effects.
● Modification of the receptor and novel spacer region to enhance specificity and functionality
● Potential to minimize the use of chemotherapy and its associated complications
● Promising advancements in the treatment of hematologic malignancies
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