IGM Biosciences has been granted a patent for binding molecules that include modified antibodies with a binding moiety that antagonizes a T-cell inhibitory signaling pathway. The antibodies can be IgM, IgA, IgG/IgM, or IgG/IgA antibodies and can form pentamers. The modified J-chain of the antibodies contains the binding moiety, which can bind to cell surface proteins involved in T-cell inhibition. GlobalData’s report on IGM Biosciences gives a 360-degree view of the company including its patenting strategy. Buy the report here.
According to GlobalData’s company profile on IGM Biosciences, personalized cancer vaccines was a key innovation area identified from patents. IGM Biosciences's grant share as of June 2023 was 1%. Grant share is based on the ratio of number of grants to total number of patents.
Patent granted for modified antibodies that antagonize t-cell inhibitory signaling
A recently granted patent (Publication Number: US11639389B2) describes an antibody with potential applications in cancer treatment. The antibody consists of five IgM antibody monomers or five IgG/IgM antibody monomers that form a pentamer. It also includes a modified J-chain, which contains a binding moiety that antagonizes a T-cell inhibitory signaling pathway. The binding moiety is attached to the modified J-chain at either the C- or N-terminus of the binding moiety or between cysteine residues 92 and 101 of the modified J-chain. The modified J-chain binds to a cell surface protein, such as CTLA4, PD-1, TIM3, LAG3, BTLA, VISTA, or TIGIT.
The antibody monomers in the composition have antigen-binding sites that can either antagonize a T-cell inhibitory signaling pathway or agonize a T-cell stimulatory signaling pathway. The antigen-binding sites can bind to various targets, including PD-1, PD-L1, TIM3, LAG3, CD137, OX40, CD40, GITR, CD27, HVEM, EGFR, HER2, HER3, EpCAM, CEACAM, Gp100, MAGE1, PD-L1, NY-ESO-1, Sialyl Lewis X antigen, Tn antigen, CD19, CD20, CD22, CD33, CD38, CD52, and CD70.
The modified J-chain is attached to SEQ ID NO: 1, either directly or indirectly via a peptide linker. The introduction of the binding moiety into the native human J-chain sequence of SEQ ID NO: 1 can be achieved through chemical or chemo-enzymatic derivatization. Additionally, a cleavable or non-cleavable chemical linker can be used to introduce the binding moiety into SEQ ID NO: 1.
The binding moiety of the modified J-chain can take various forms, including antigen-binding fragments of antibodies, antibody-drug conjugates, antibody-like molecules, antigen-binding fragments of antibody-like molecules, ligands, and receptors. Specifically, the binding moiety can be an antigen-binding fragment of an antibody, such as F(ab')2, Fab', Fab, Fv, scFv, or single domain antibody.
The patent also mentions a pharmaceutical composition for the treatment of cancer, which includes an effective amount of the antibody described above and a pharmaceutically acceptable carrier.
Overall, this patent describes an antibody with a modified J-chain that can bind to specific cell surface proteins and has the potential to antagonize or agonize T-cell signaling pathways. The antibody's ability to bind to a wide range of targets makes it a promising candidate for cancer treatment.
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