US2020101080A1PendingUtilityA1
Inhibitors of dna pk and uses thereof
Est. expiryMar 31, 2037(~10.7 yrs left)· nominal 20-yr term from priority
A61K 31/5377A61K 31/7088A61P 37/06A61K 9/0019A61K 9/0014A61K 9/0053
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Claims
Abstract
The present disclosure relates to compositions and methods for improving the transplantation outcome and/or reducing immune response in a subject. The compositions comprise a DNA-PK inhibitor.
Claims
exact text as granted — not AI-modified1 . A method of improving the transplantation outcome in a subject receiving an organ transplant, the method comprising administering to the subject a therapeutically effective amount of a composition comprising a DNA-PK inhibitor, wherein the DNA-PK inhibitor improves the transplantation outcome.
2 . The method of claim 1 , wherein the improvement in transplantation outcome is reduced graft rejection or increased graft survival.
3 . The method of claim 2 , wherein the reduced graft rejection is reduced chronic graft rejection or reduced acute graft rejection.
4 . (canceled)
5 . The method of claim 1 , wherein the organ transplant is an allograft or xenograft.
6 .- 7 . (canceled)
8 . The method of claim 1 , wherein the DNA-PK inhibitor suppresses T or B cell activity.
9 . The method of claim 8 , wherein the DNA-PK inhibitor suppresses T and B cell activity.
10 .- 11 . (canceled)
12 . The method of claim 1 , wherein the DNA-PK inhibitor suppresses IL-2 secretion in T-cells.
13 . (canceled)
14 . The method of claim 1 , wherein the improvement in transplantation outcome is decreased lymphocytic infiltration, vasculitis, infarction, ischemia, thrombosis, intimal thickening, glomerular atrophy, glomerular sclerosis, tubular atrophy, hyalinization, interstitial fibrosis, cortical fibrosis, serum creatinine levels, intimal proliferation, hypertrophy, cardiac vessel disease post-transplant, graft intimal hyperplasia, luminal occlusion, or bronchitis obliterans.
15 . The method of claim 1 , wherein the subject is the recipient of an organ tissue transplant, said organ tissue selected from the group consisting of kidney, liver, heart, lung, bone marrow, and cornea tissue.
16 . The method of claim 1 , wherein the DNA-PK inhibitor composition is administered by intravascular, intravenous, intra-arterial, subcutaneous, intramuscular, intraperitoneal, intraventricular, or intraepidural administration.
17 . (canceled)
18 . The method of claim 1 , wherein the DNA-PK inhibitor is selected from the group consisting of a small-molecule inhibitor, nucleotide inhibitor, and antibody inhibitor, wherein the DNA-PK inhibitor reduces DNA-PK activity.
19 . A method of reducing immune response in a subject in need thereof, the method comprising administering to the subject a therapeutically effective amount of a composition comprising a DNA-PK inhibitor, wherein the DNA-PK inhibitor reduces an immune response.
20 . The method of claim 19 , wherein the DNA-PK inhibitor reduces or blocks an immune response already in progress.
21 . The method of claim 19 , wherein the DNA-PK inhibitor prevents the induction of an immune response.
22 . The method of claim 19 , wherein the DNA-PK inhibitor suppresses T or B cell activity.
23 . The method of claim 19 , wherein the DNA-PK inhibitor suppresses T and B cell activity.
24 .- 25 . (canceled)
26 . The method of claim 19 , wherein the DNA-PK inhibitor is selected from the group consisting of a small-molecule inhibitor, nucleotide inhibitor, and antibody inhibitor, wherein the DNA-PK inhibitor reduces DNA-PK activity.
27 . The method of claim 19 , wherein the DNA-PK inhibitor composition is administered orally, parenterally, or topically.
28 . (canceled)
29 . A method of treating an IL-2 related disease in a subject in need thereof, the method comprising administering to the subject a therapeutically effective amount of a composition comprising a DNA-PK inhibitor, wherein the DNA-PK inhibitor suppresses humoral or cellular immunity.
30 . The method of claim 29 , wherein the IL-2 related disease is one or more of AIDS, psoriasis, atopic dermatitis, urticaria, lupus nephritis, allergic conjunctivitis, sty, chalazion, spring catarrh, uveitis, polymyositis, Hashimoto's disease, Behcet's disease, ankylosing spondylitis, systemic sclerosis, Sjogren's syndrome, pollenosis, scleroderma), gastrointestinal diseases, gout, psoriatic arthritis, rheumatoid arthritis, multiple sclerosis, asthma, chronic obstructive pulmonary disease, fibromyalgia, myasthenia gravis, sarcoidosis, nasal inflammation and nasal catarrh.
31 .- 32 . (canceled)Cited by (0)
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