Sorrento Therapeutics has been granted a patent for variant anti-OX40 antibodies that mimic the activity of OX40L, enhancing T cell clonal expansion and differentiation. The antibodies have improved binding affinity and agonistic activity compared to the wild type antibody. They specifically bind to OX40 receptors on activated T lymphocytes, stimulate proliferation of effector T cells, and stimulate production of cytokines. GlobalData’s report on Sorrento Therapeutics gives a 360-degree view of the company including its patenting strategy. Buy the report here.
According to GlobalData’s company profile on Sorrento Therapeutics, Personalized cancer vaccines was a key innovation area identified from patents. Sorrento Therapeutics's grant share as of September 2023 was 36%. Grant share is based on the ratio of number of grants to total number of patents.
Variant anti-ox40 antibody for enhancing t cell expansion
A recently granted patent (Publication Number: US11773177B2) discloses an anti-OX40 antibody and its use in various methods for inducing proliferation and cytokine production in effector T cells. The antibody, or an antigen binding fragment thereof, specifically binds to an OX40 epitope and is characterized by a heavy chain variable domain with a specific amino acid sequence (SEQ ID NO. 9) and a light chain variable domain with another specific amino acid sequence (SEQ ID NO. 7).
The patent claims cover different aspects of the anti-OX40 antibody. Claim 1 describes the antibody or antigen binding fragment, while claim 2 specifies that the antibody is of the IgG isotype. Claim 3 encompasses various antibody formats, including Fab, Fab', F(ab')2, Fv, domain antibody, single chain antibody, diabody, triabody, and tetrabody. Claim 4 includes a polypeptide comprising the antibody or antigen-binding fragment.
The patent also discloses methods for inducing proliferation of effector T cells using the anti-OX40 antibody. Claim 6 describes a method where effector T cells are contacted with the antibody, leading to their proliferation. Claim 7 adds the step of detecting an increase in proliferation of the effector T cells. Claim 8 further includes contacting the effector T cells with CD3. Claim 9 specifies that the effector T cells are CD4+ effector T cells.
Additionally, the patent covers methods for inducing effector T cells to increase production of cytokines. Claim 10 describes a method where effector T cells are contacted with the anti-OX40 antibody, resulting in increased cytokine production. Claim 11 adds the step of detecting an increase in cytokine production by the effector T cells. Claim 12 specifies that the cytokines can include gamma-interferon, IL-2, IL-4, and tumor necrosis factor (TNF). Claim 13 includes contacting the effector T cells with CD3, and claim 14 specifies that the effector T cells are CD4+ effector T cells.
Furthermore, the patent discloses a method for inducing proliferation of effector T cells in the presence of regulatory T cells. Claim 15 describes a method where both effector T cells and regulatory T cells are contacted with the anti-OX40 antibody, leading to increased proliferation of the effector T cells. Claim 16 adds the step of detecting an increase in proliferation of the effector T cells. Claim 17 includes contacting the effector T cell and the regulatory T cell with CD3. Claim 18 specifies that the effector T cells express CD25, and claim 19 states that the effector T cells produce at least one cytokine selected from IL-2, IL-4, and INF?.
In summary, the granted patent discloses an anti-OX40 antibody and its use in various methods for inducing proliferation and cytokine production in effector T cells. The antibody specifically binds to an OX40 epitope and can be of the IgG isotype. The methods involve contacting the effector T cells with the antibody, optionally in combination with CD3, and can be applied to CD4+ effector T cells. These findings have potential implications for the development of immunotherapies targeting T cell responses.
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