IP Library Granted Patent US 9,512,209
Granted Patent B2
US 9,512,209 · App. 14/219,857 · Granted Dec 6, 2016

Methods of modulating inflammasome activity to treat inflammatory conditions

Inventors: Robert W. Keane (Miami, FL); W. Dalton Dietrich (Miami, FL); Juan Pablo De Rivero Vaccari (Miami, FL); Helen M. Bramlett (Miami, FL)
Assignee: University of Miami
C07K16/18A61K39/395A61K2039/505C07K2317/76C07K2317/77
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Quick Facts
Patent No.
US 9,512,209
App. No.
14/219,857
Granted
Dec 6, 2016
Kind
B2
Abstract

Compositions and methods for reducing inflammation in the central nervous system (CNS) of a mammal that has been subjected to a stroke, traumatic injury to the CNS such as traumatic brain injury (TBI), spinal cord injury (SCI), or having an autoimmune or CNS disease have been developed. The compositions and methods described herein include antibodies that specifically bind to at least one component (e.g., ASC, NALP1) in a mammalian inflammasome (e.g., the NALP1 inflammasome) and have use as treatments for SCI, TBI, stroke, and autoimmune and CNS diseases in a mammal. In a rodent model of SCI, therapeutic neutralization of ASC using a polyclonal antibody that specifically binds to ASC inhibited the inflammasome, reduced caspase-1 activation, XIAP cleavage, and interleukin processing, resulting in significant tissue sparing and functional improvement. Additionally, in a rodent model of TBI, neutralization of ASC after TBI reduced caspase-1 activation and XIAP cleavage. Further, in a rodent thromboembolic stroke model, neutralization of NLRP1 resulted in reduced histopathological damage in mice and reduced cytokine activation, suggesting that the inflammasome complex forms in the brain after stroke and is a therapeutic target for reducing the detrimental consequences of post-stroke inflammation.

Claims (19)

1. A method for treating inflammation associated with a central nervous system (CNS) injury or an autoimmune or neurodegenerative disease in a subject in need thereof comprising administering to the subject an antibody that specifically binds to at least one component of a mammalian inflammasome comprising Nacht Leucine-Rich-Repeat Protein 1 (NALP1), wherein the antibody specifically binds to NALP1; wherein the administering the antibody reduces levels of at least one inflammatory cytokine, thereby treating the inflammation in the patient.

2. The method of claim 1 , wherein the autoimmune or neurodegenerative disease is amyotrophic lateral sclerosis, Alzheimer's disease, Parkinson's disease, muscular dystrophy, or multiple sclerosis.

3. The method of claim 1 , wherein the inflammation in the CNS of the subject is reduced following administration of the antibody.

4. The method of claim 1 , wherein the antibody is administered by a parenteral route of administration.

5. The method of claim 4 , wherein the parenteral route of administration is intravenous, subcutaneous, intramuscular, intraperitoneal, or intrathecal.

6. The method of claim 1 , wherein the antibody is administered intracerebroventricularly.

7. The method of claim 1 , wherein administering the antibody results in improvement in motor skills and locomotor function or cognition in the subject.

8. The method of claim 1 , wherein the antibody is a monoclonal antibody.

9. The method of claim 1 , wherein the antibody is a polyclonal antibody.

10. The method of claim 1 , wherein the antibody is taken up by cells in the CNS.

11. The method of claim 1 , wherein administering the antibody results in inhibition of inflammasome activation in the subject.

12. The method of claim 1 , wherein administering the antibody results in a reduction of caspase-1 activation and XIAP cleavage in the CNS of the subject.

13. The method of claim 1 , wherein the antibody is formulated with a pharmaceutically acceptable carrier or diluent.

14. The method of claim 1 , wherein the at least one component of the mammalian inflammasome is intracellular.

15. The method of claim 1 , wherein the CNS injury is traumatic brain injury, stroke, or spinal cord injury.

16. The method of claim 1 , wherein the at least one inflammatory cytokine is interleukin-1 β (IL-1β) or interleukin-18.

17. The method of claim 1 , further comprising administering a battery of tasks to assess a functional outcome of administering the antibody.

18. The method of claim 1 , wherein the antibody binds to a NALP1 amino acid sequence having at least 85% sequence identity with SEQ ID NO:3.

19. A method for treating inflammation associated with a CNS injury or an autoimmune or neurodegenerative disease in a subject in need thereof comprising administering to the subject an antibody that specifically binds to at least one component of a NALP1 mammalian inflammasome, wherein the antibody specifically binds to an amino acid sequence having at least 85% sequence identity with SEQ ID NO: 3, wherein said inflammation in said patient is treated.

Assignments (2)
CONFIRMATORY LICENSE Recorded Mar 25, 2022
From: UNIVERSITY OF MIAMI SCHOOL OF MEDICINE
To: UNITED STATES GOVERNMENT
Reel/Frame 059510/0855 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 19, 2016
From: KEANE, ROBERT W.; DIETRICH, W. DALTON; VACCARI, JUAN PABLO DE RIVERO; BRAMLETT, HELEN M.
To: UNIVERSITY OF MIAMI
Reel/Frame 039191/0603 →
Continuity (3)
Continuation 12182886 · Jul 30, 2008
Provisional Application 60952757 · Jul 30, 2007
Related Publication 20140286956A1 · Sep 25, 2014