IP Library Granted Patent US 11,053,290
Granted Patent B2
US 11,053,290 · App. 15/771,036 · Granted Jul 6, 2021

Modified Tamm-Horsfall protein and related compositions and methods of use

Inventors: Tarek Maurice Ashkar (Zionsville, IN); Radmila Micanovic (Indianapolis, IN)
Assignees: Indiana University Research and Technology Corporation; The United States Government as Represented by the Department of Veterans Affair
C07K14/47A61P13/12C07K14/435A61K35/00A61K35/22A61K38/00A61K38/1709
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Quick Facts
Patent No.
US 11,053,290
App. No.
15/771,036
Granted
Jul 6, 2021
Kind
B2
Abstract

Embodiments of the present disclosure provide polypeptides, related materials and compositions, and methods for their use. In certain embodiments, the present disclosure provides a monomeric Tamm-Horsfall Protein polypeptide, or a biologically active truncation thereof. Other embodiments provide polynucleotides encoding a polypeptide described herein, nucleic acid expression vectors including the polynucleotides, and recombinant host cells including the expression vector. Yet other embodiments provide pharmaceutical compositions including a polypeptide described herein. Also provided are methods for treating a renal disease, disorder, or condition in a subject and/or modulating an immune response in a subject.

Claims (19)

1. A purified or isolated polypeptide consisting of an amino acid sequence at least 95% identical to an amino acid sequence chosen from SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO:6, and SEQ ID NO: 7.

2. The purified or isolated polypeptide of claim 1 , wherein the purified or isolated polypeptide consists of an amino acid sequence chosen from SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO:6, and SEQ ID NO: 7.

3. A pharmaceutical composition comprising the purified or isolated polypeptide of claim 1 and a pharmaceutically acceptable carrier.

4. The pharmaceutical composition of claim 3 , further comprising a purified or isolated polypeptide comprising an amino acid sequence at least 85% identical to an amino acid sequence according to SEQ ID NO: 1.

5. A method for treating at least one renal disease, disorder, or condition in a subject, the method comprising administering to the subject an effective amount of the purified or isolated polypeptide of claim 1 , or both the purified or isolated polypeptide of claim 1 and a purified or isolated polypeptide comprising an amino acid sequence at least 85% identical to an amino acid sequence according to SEQ ID NO: 1, wherein the at least one renal disease, disorder, of condition comprises at least one of: acute kidney injury, sepsis, transplant rejection, and chronic kidney disease.

6. The method according to claim 5 , wherein the polypeptide or the pharmaceutical composition is administered orally, intravenously, intraperitoneally, intramuscularly, or subcutaneously.

7. The method according to claim 5 , wherein the effective amount is between about 0.2 mg/kg and about 10.0 mg/kg of the polypeptide.

8. The method according to claim 5 , wherein the effective amount is between about 0.2 mg/kg and about 3.0 mg/kg of the polypeptide.

9. A method for treating at least one renal disease, disorder, or condition in a subject, the method comprising administering to the subject an effective amount of the pharmaceutical composition of claim 3 , or a pharmaceutical composition of claim 3 further comprising a polypeptide comprising an amino acid sequence at least 85% identical to an amino acid sequence according to SEQ ID NO: 1, wherein the at least one renal disease, disorder, of condition comprises at least one of: acute kidney injury, sepsis, transplant rejection, and chronic kidney disease.

10. The method according to claim 9 , wherein the polypeptide or the pharmaceutical composition is administered orally, intravenously, intraperitoneally, intramuscularly, or subcutaneously.

11. The method according to claim 9 , wherein the effective amount is between about 0.2 mg/kg and about 10.0 mg/kg of the polypeptide.

12. The method according to claim 9 , wherein the effective amount is between about 0.2 mg/kg and about 3.0 mg/kg of the polypeptide.

13. An immunogenic composition comprising at least one immunogenic agent and the purified or isolated polypeptide of claim 1 .

14. A method for enhancing an immune response to an immunogenic composition in a subject, the method comprising administering to the subject an effective amount of the purified or isolated polypeptide of claim 1 .

15. A purified or isolated polypeptide consisting of an amino acid sequence at least 95% identical to SEQ ID NO: 7.

16. A pharmaceutical composition comprising the purified or isolated polypeptide of claim 15 and a pharmaceutically acceptable carrier.

17. A method for treating at least one renal disease, disorder, or condition in a subject, the method comprising administering to the subject an effective amount of the purified or isolated polypeptide of claim 15 .

18. The purified or isolated polypeptide of claim 1 , further comprising a polypeptide half-life increasing compound or a peptide purification tag linked to the isolated polypeptide.

19. The purified or isolated polypeptide of claim 15 , further comprising polypeptide half-life increasing compound or a peptide purification tag linked to the isolated polypeptide.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 30, 2020
From: INDIANA UNIVERSITY RESEARCH AND TECHNOLOGY CORPORATION
To: INDIANA UNIVERSITY RESEARCH AND TECHNOLOGY CORPORATION; THE UNITED STATES GOVERNMENT AS REPRESENTED BY THE DEPARTMENT OF VETERANS AFFAIRS
Reel/Frame 052534/0153 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 25, 2018
From: ASHKAR, TAREK; MICANOVIC, RADMILA
To: INDIANA UNIVERSITY RESEARCH AND TECHNOLOGY CORPORATION
Reel/Frame 045636/0712 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 25, 2018
From: ASHKAR, TAREK MAURICE; MICANOVIC, RADMILA
To: INDIANA UNIVERSITY RESEARCH AND TECHNOLOGY CORPORATION
Reel/Frame 045636/0814 →
Continuity (3)
Provisional Application 62401759 · Sep 29, 2016
Provisional Application 62248809 · Oct 30, 2015
Related Publication 20180305420A1 · Oct 25, 2018