US2013158100A1PendingUtilityA1
Intracellular dna receptor
Est. expirySep 26, 2028(~2.2 yrs left)· nominal 20-yr term from priority
A61P 31/00C12N 15/85G01N 33/564A61P 31/12A61P 31/04G01N 2800/24A61K 31/7105A61K 31/713G01N 33/5035
42
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Claims
Abstract
Provided herein are methods of identifying and using compounds that modulate an AIM2 polypeptide-mediated immune response. Further provided herein are methods of treating disease comprising administering to a patient a compound that decreases expression of an AIM2 polypeptide. Further provided herein are methods of providing gene therapy to a patient comprising administering to the patient a gene therapy agent and a compound that decreases expression of an AIM2 polypeptide. In certain embodiments, a compound that decreases expression of an AIM2 polypeptide comprises an siRNA or an shRNA.
Claims
exact text as granted — not AI-modified1 . A method of treating an autoimmune disease in a patient, comprising administering to the patient a compound that decreases expression of an AIM2 polypeptide.
2 . The method of claim 1 , wherein the compound comprises an siRNA or an shRNA.
3 . The method of claim 1 , wherein expression of the AIM2 polypeptide is decreased by at least 50%.
4 . The method of claim 1 , wherein the disease is selected from the group consisting of: rheumatoid arthritis, systemic lupus erythematosis, scleroderma, dermatomyositis, and psoriasis.
5 . A method of treating an infection comprising administering to a patient a compound that decreases expression of an AIM2 polypeptide.
6 . The method of claim 5 , wherein the compound comprises an siRNA or an shRNA.
7 . The method of claim 5 , wherein expression of the AIM2 polypeptide is decreased by 50%.
8 . The method of claim 5 , wherein the infection is caused by a bacterial pathogen.
9 . The method of claim 8 , wherein the bacterial pathogen is selected from the group consisting of Shigella spp., Francisella spp. Chlamyida spp. Listeria monocytogenes, Mycobacterium tuberculosis, Mycobacterium leprae, Mycobacterium avium intracellulare, Brucella spp., Salmonella spp., Legionella, and Rickettsia.
10 . The method of claim 5 , wherein the infection is caused by a viral pathogen.
11 . The method of claim 10 , wherein the viral pathogen is a member of a viral family selected from the group consisting of: Adenoviridae, Picornaviridae, Herpesviridae, Hepadnaviridae, Flaviviridae, Retroviridae, Orthomyxoviridae, Paramyxoviridae, Papovaviridae, Rhabdoviridae and Togaviridae.
12 - 19 . (canceled)
20 . A method of introducing a double-stranded DNA molecule into a cell comprising:
administering to the cell a compound that decreases expression of an AIM2 polypeptide; contacting the cell with the double-stranded DNA molecule under transfection conditions such that the cell is transfected with the double-stranded DNA molecule.
21 . The method of claim 20 , wherein the compound comprises an siRNA or an shRNA.
22 . The method of claim 20 , wherein expression of the AIM2 polypeptide is decreased by at least 50%.
23 . The method of claim 20 , wherein the double-stranded DNA molecule comprises a portion encoding a polypeptide.
24 . The method of claim 20 , wherein the cell is a mammalian cell.
25 . The method of claim 20 , wherein the cell is a dendritic cell.
26 . The method of claim 20 , wherein the cell is a monocyte.Cited by (0)
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