Allogene Therapeutics has been granted a patent for polynucleotides encoding CD19-specific CARs that resist rituximab binding, along with methods for making and using these CARs in immune cells like CAR-T cells. The patent claim specifies the sequence and promoter required for expression in mammalian T cells. GlobalData’s report on Allogene Therapeutics gives a 360-degree view of the company including its patenting strategy. Buy the report here.
According to GlobalData’s company profile on Allogene Therapeutics, Cytokine activate T-cell based compositions was a key innovation area identified from patents. Allogene Therapeutics's grant share as of February 2024 was 6%. Grant share is based on the ratio of number of grants to total number of patents.
Patent granted for cd19-specific cars resistant to rituximab
A recently granted patent (Publication Number: US11896617B2) discloses an isolated polynucleotide encoding a polypeptide with an anti-CD19 chimeric antigen receptor (CAR) that lacks a rituximab binding site. The polynucleotide includes a nucleic acid sequence with at least 90% identity to a specific sequence and a short EF1a promoter for expression in mammalian T cells. Additionally, the polypeptide may contain a safety switch, a CD34 epitope, and a CD8 hinge/transmembrane domain, among other features.
Furthermore, the patent covers a vector containing the isolated polynucleotide, various engineered immune cells expressing the anti-CD19 CAR, and pharmaceutical compositions comprising these cells and a pharmaceutically acceptable excipient. The engineered immune cells, which can be T cells, NK cells, dendritic cells, or others, are designed to be resistant to rituximab and may be either autologous or allogeneic. The patent also specifies different levels of nucleic acid sequence identity to a particular sequence, ranging from 95% to 99%, further detailing the composition and characteristics of the disclosed polynucleotide.
To know more about GlobalData’s detailed insights on Allogene Therapeutics, buy the report here.
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