US2020062846A1PendingUtilityA1
Immunopotentiative composition
Est. expiryJul 3, 2022(expired)· nominal 20-yr term from priority
A61P 35/00A61P 37/04A61P 31/12A61P 43/00A61P 35/04A61P 31/00A61P 31/16A61P 31/20A61P 31/14A61P 33/06A61P 37/06A61P 31/10A61P 35/02A61P 31/22A61P 31/18A61P 31/04A61P 11/00A61P 1/16G01N 33/575C07K 14/70521A61K 39/3955C07K 2317/73A61K 2039/505C07K 2317/24C07K 16/2818C07K 2317/76A61K 31/7088C07K 16/2803G01N 33/5011A61K 9/0019A61K 38/212A61K 38/1774C12Q 1/025C07K 16/2827G01N 2500/00A61K 47/02C07K 2319/30C07K 2317/54C07K 2317/21A61K 2039/507A61K 47/26C07K 16/18A61K 45/06Y02A50/394Y02A50/39Y02A50/466Y02A50/463G01N 33/574Y02A50/30
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Claims
Abstract
The compositions of the present invention that inhibits the function of PD-1, PD-L1, or PD-L2 are useful for cancer or infection treatment.
Claims
exact text as granted — not AI-modified1 . (canceled)
2 . A method of treating a tumor in a subject in need thereof comprising administering to the subject an immunosuppressive signal inhibitor of PD-1, PD-L1, or PD-L2.
3 . The method of claim 2 , wherein the immunosuppressive signal inhibitor suppresses cancer metastasis.
4 . A method of treating an infection in a subject in need thereof comprising administering to the subject an immunosuppressive signal inhibitor of PD-1, PD-L1 or PD-L2.
5 . The method of claim 2 , wherein the immunosuppressive signal inhibitor acts through immunopotentiation.
6 . The method of claim 4 , wherein the immunosuppressive signal inhibitor acts through immunopotentiation.
7 . The method of claim 2 , wherein the immunosuppressive signal inhibitor is one or more selected from the group consisting of an interaction inhibitor of PD-1 and PD-L1 or PD-1 and PD-L2, an intracellular signaling inhibitor of PD-1, and a production inhibitor of PD-1, PD-L1 or PD-L2.
8 . The method of claim 7 , wherein the interaction inhibitor of PD-1 and PD-L1 is one or more selected from the group consisting of an anti-PD-1 antibody, an anti-PD-L1 antibody, soluble PD-1, and soluble PD-L1.
9 . The method of claim 8 , wherein the anti-PD-1 antibody is selected from the group consisting of an anti-human PD-1 antibody produced by a hybridoma internationally deposited as FERM BP-8392, a humanized anti-human PD-1 antibody, and a human anti-human PD-1 antibody.
10 . The method of claim 2 , wherein the immunosuppressive signal inhibitor is a lymphocyte in which PD-1 expression is inhibited by gene-recombination.
11 . The method of claim 7 , wherein the interaction inhibitor of PD-1 and PD-L1 or PD-1 and PD-L2, the intracellular signaling inhibitor of PD-1, or the production inhibitor of PD-1, PD-L1 or PD-L2 is one or more substances selected from a protein, a polypeptide, a peptide, a polynucleotide, a polynucleoside, an antibody or a derivative thereof, an organic synthesis compound, an inorganic compound, and a natural product.
12 - 28 . (canceled)
29 . A method of screening for a substance for treatment of cancer, comprising contacting a test substance with a carcinoma cell expressing PD-L1 or PD-L2 and a lymphocyte, wherein the test substance enhances an immune reaction of the lymphocyte to the carcinoma cell and thereby inhibits carcinoma cell proliferation.
30 . A method of screening for a substance for treatment of infection, comprising contacting a test substance with a cell, which expresses PD-L1 or PD-L2 and is infected with a pathogen and a lymphocyte, wherein the test substance enhances immune reaction of the lymphocyte to the infected cell and thereby inhibits pathogen proliferation.
31 - 32 . (canceled)Cited by (0)
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