IP Library Granted Patent US 10,232,023
Granted Patent B2
US 10,232,023 · App. 15/441,982 · Granted Mar 19, 2019

Methods for treatment of and prophylaxis against inflammatory disorders

Inventors: Christian Con Yost (North Salt Lake, UT); Guy A. Zimmerman (Salt Lake City, UT); Andrew S. Weyrich (Salt Lake City, UT)
Assignee: UNIVERSITY OF UTAH RESEARCH FOUNDATION
A61K38/57A61K38/1709C07K14/4703A61K38/00Y02A50/385Y02A50/387Y02A50/473
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Quick Facts
Patent No.
US 10,232,023
App. No.
15/441,982
Granted
Mar 19, 2019
Kind
B2
Abstract

An isolated and purified peptide, neonatal NET-inhibitory Factor (nNIF), is disclosed. Methods for treatment of and prophylaxis against inflammatory disorders are also disclosed, including methods of treatment of and prophylaxis against inflammatory disorders comprising administering NET-inhibitory peptides (NIPs), which may be a nNIF, a pharmaceutically acceptable salt of a nNIF, a nNIF analog, a pharmaceutically acceptable salt of a nNIF analog, a nNIF-Related Peptide (nNRP), including the nNRP, Cancer-Associated SCM-Recognition, Immune Defense Suppression, and Serine Protease Protection Peptide (CRISPP), a pharmaceutically acceptable salt of a nNRP, a nNRP analog, or a pharmaceutically acceptable salt of a nNRP analog, to an individual.

Claims (13)

1. A method for treating neutrophil extracellular trap (NET) mediated inflammatory tissue damage in a patient, comprising:

administering to the patient an effective amount of a pharmaceutical composition comprising a peptide consisting of the amino acid sequence of SEQ ID NO:1, SEQ ID NO:2 or SEQ ID NO:4 and a pharmaceutically acceptable carrier to reduce a pathological effect or symptom of the NET-mediated inflammatory tissue damage.

2. The method of claim 1 , wherein the pharmaceutical composition substantially inhibits NET-mediated inflammatory tissue damage.

3. The method of claim 1 , wherein at least one amino acid of SEQ ID NO:1 or SEQ ID NO:2 or SEQ ID NO:4 is bound to a chemical modifier, and

wherein the chemical modifier is selected from at least one of a lipid, a polyethylene glycol (PEG), or a saccharide.

4. The method of claim 1 , wherein the peptide consisting of SEQ ID NO:1 or SEQ ID NO:2 or SEQ ID NO:4 does not globally depress polymorphonuclear leukocyte (PMN) function.

5. The method of claim 1 , wherein the peptide consisting of SEQ ID NO:1 or SEQ ID NO:2 or SEQ ID NO:4 does not substantially inhibit one or more activities of a polymorphonuclear leukocyte (PMN) selected from the group consisting of chemotaxis, chemokine synthesis and secretion, cytokine synthesis and secretion, extracellular bacterial killing, intracellular bacterial killing, phagocytosis, and reactive oxygen species (ROS) generation.

6. The method of claim 1 , wherein the peptide consisting of SEQ ID NO:1 or SEQ ID NO:2 or SEQ ID NO:4 is present in an amount effective to substantially inhibit NET formation.

7. The method of claim 6 , wherein the NET formation is stimulated by at least one of a bacterium, a fungus, a parasite, or a virus.

8. A method for inhibiting neutrophil extracellular trap (NET) formation in a patient comprising:

administering to the patient an effective amount of a pharmaceutical composition comprising a peptide consisting of the amino acid sequence of SEQ ID NO:1, SEQ ID NO:2 or SEQ ID NO:4 and a pharmaceutically acceptable carrier to substantially inhibit NET formation.

9. The method of claim 8 , wherein the NET formation is stimulated by a virus selected from at least one of a hemorrhagic fever virus, a Filovirus, an arenavirus, a hantavirus, a flavivirus, dengue virus, yellow fever virus, or HIV-1.

10. The method of claim 8 , wherein the NET formation is stimulated by a bacterium selected from at least one of a Bacillus species, an Escherichia species, a Francisella species, a Staphylococcus species, a Streptococcus species, or a Yersinia species.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 18, 2019
From: YOST, CHRISTIAN CON; ZIMMERMAN, GUY A.; WEYRICH, ANDREW S.
To: UNIVERSITY OF UTAH
Reel/Frame 048060/0264 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 18, 2019
From: UNIVERSITY OF UTAH
To: UNIVERSITY OF UTAH RESEARCH FOUNDATION
Reel/Frame 048060/0277 →
Continuity (3)
Division 14904048
Provisional Application 61843618 · Jul 8, 2013
Related Publication 20170232081A1 · Aug 17, 2017