Fate Therapeutics has been granted a patent for identifying compounds that enhance immune cells for adoptive cell therapies. The method involves culturing immune cells to increase specific subpopulations, improving efficacy in treating human subjects. GlobalData’s report on Fate Therapeutics gives a 360-degree view of the company including its patenting strategy. Buy the report here.
According to GlobalData’s company profile on Fate Therapeutics, T-cell culturing was a key innovation area identified from patents. Fate Therapeutics's grant share as of April 2024 was 18%. Grant share is based on the ratio of number of grants to total number of patents.
Cell therapy for treating human subjects with modulated immune cells
A recently granted patent (Publication Number: US11932870B2) discloses a method for treating a human subject by administering a therapeutic composition containing modulated immune cells. These immune cells are produced by culturing a population of immune cells in a culture medium with the inhibition of BCR-ABL tyrosine kinase, leading to an increase in specific subpopulations of T cells expressing CD62L and CCR7. The therapeutic composition, containing these modulated T cells, is administered in a therapeutically effective amount for adoptive cell therapy in the human subject in need.
Furthermore, the patent claims cover various aspects of the method, including the preparation of the therapeutic composition by isolating specific subpopulations of T cells, the source of the immune cells from various tissues or subjects with different health conditions, the differentiation of immune cells from different types of stem cells or progenitor cells, and the genomic engineering of immune cells to express specific receptors. The method also involves inhibiting BCR-ABL tyrosine kinase using a specific compound, resulting in the modulation of T cells with specific gene expressions and memory subpopulations. Additionally, the patent covers the use of CAR-T cells and specifies the inclusion of CD8+ or CD4+ T cells in the therapeutic composition.
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