IP Library › Granted Patent US 11,834,519
Granted Patent B2
US 11,834,519 · App. 16/294,733 · Granted Dec 5, 2023

Compositions and methods for modulating γ-c-cytokine activity

Inventors: Yutaka Tagaya (Rockville, MD); Nazli Azimi (San Juan Capistrano, CA)
Assignee: BIONIZ THERAPEUTICS, INC.
C07K7/08A61K8/64A61K38/20A61K47/642A61K47/643A61Q3/00A61Q7/00A61Q19/00A61Q19/004A61Q19/08C07K7/06C07K14/52C07K14/54C12N15/00A61K38/00A61K38/10
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Quick Facts
Patent No.
US 11,834,519
App. No.
16/294,733
Granted
Dec 5, 2023
Kind
B2
Abstract

The γc-family cytokines, Interleukin-2 (IL-2), Interleukin-4 (IL-4), Interleukin-7 (IL-7), Interleukin-9 (IL-9), Interleukin-15 (IL-15), and Interleukin-21 (IL-21), are associated with important human diseases, such as leukemia, autoimmune diseases, collagen diseases, diabetes mellitus, skin diseases, degenerative neuronal diseases and graft-versus-host disease (GvHD). Thus, inhibitors of γc-cytokine activity are valuable therapeutic and cosmetic agents as well as research tools. Peptide and/or peptide derivative antagonists based on the consensus γc-subunit binding site to inhibit γc-cytokine activity are described. Also described are peptide and/or peptide derivative antagonists exhibiting Simul-Block activity, and inhibiting the activity of multiple γc-cytokine family members.

Claims (26)

1. A nucleotide sequence encoding a composite peptide that comprises amino acid sequences of at least two interleukin (IL) protein gamma-c-box D-helix regions, wherein the composite peptide comprises an amino acid sequence Xaa Phe Leu Xaa Xaa Xaa Xaa Xaa Xaa Xaa Gln (SEQ ID NO: 2), wherein the Xaa at position 1 is D or E, the Xaa at position 4 is E, Q, or N, the Xaa at position 5 is S or R, the Xaa at position 6 is any amino acid, the Xaa at position 7 is I or K, the Xaa at position 8 is any amino acid, the Xaa at position 9 is L or I, the Xaa at position 10 is any amino acid.

2. The nucleotide sequence of claim 1 , wherein the composite peptide inhibits the activity of two or more γc-cytokines selected from the group consisting of IL-2, IL-4, IL-7, IL-9, IL-15, and IL-21.

3. The nucleotide sequence of claim 1 , wherein the nucleotide sequence is selected from the group consisting of dsDNA, ssDNA, dsRNA, and ssRNA.

4. The nucleotide sequence of claim 1 , wherein the composite peptide comprises the amino acid sequence I-K-E-F-L-Q-R-F-I-H-I-V-Q-S-I-I-N-T-S(SEQ ID NO: 1) (BNZ-γ).

5. A pharmaceutical composition comprising:

a nucleotide sequence encoding a peptide conjugate; and

a pharmaceutically acceptable carrier, diluent, excipient or combination thereof;

wherein the peptide conjugate inhibits the activity of two or more γc-cytokines selected from the group consisting of IL-2, IL-4, IL-7, IL-9, IL-15, and IL-21;

wherein the peptide conjugate thereof comprises an amino acid sequence Xaa Phe Leu Xaa Xaa Xaa Xaa Xaa Xaa Xaa Gln (SEQ ID NO: 2), wherein the Xaa at position 1 is D or E, the Xaa at position 4 is E, Q, or N, the Xaa at position 5 is S or R, the Xaa at position 6 is any amino acid, the Xaa at position 7 is I or K, the Xaa at position 8 is any amino acid, the Xaa at position 9 is L or I, the Xaa at position 10 is any amino acid.

6. The pharmaceutical composition of claim 5 , wherein the nucleotide sequence further comprises a sequence encoding a signal peptide.

7. The pharmaceutical composition of claim 5 , wherein the nucleotide sequence is selected from the group consisting of dsDNA, ssDNA, dsRNA, and ssRNA.

8. The pharmaceutical composition of claim 5 , wherein the peptide conjugate comprises the amino acid sequence I-K-E-F-L-Q-R-F-I-H-I-V-Q-S-I-I-N-T-S(SEQ ID NO: 1) (BNZ-γ).

9. A method for blocking signaling by two or more γc-cytokine family members, comprising contacting a cell with the pharmaceutical composition of claim 5 .

10. A method of inhibiting γc-cytokine binding to a γc-subunit comprising contacting a γc-subunit of a cell with the pharmaceutical composition of claim 5 .

11. A method of treating a γc-cytokine-mediated disease, the method comprising administering the pharmaceutical composition of claim 5 to a subject in need thereof, wherein the γc-cytokine-mediated disease is selected from the group consisting of myasthenia gravis, inflammatory bowel disease, CD4-leukemia, CD8-leukemia, LGL-leukemia, systemic lupus erythematosis, Sjögren's syndrome, Wegener's granulomatosis, Celiac disease, Hashimoto's thyroiditis, rheumatoid arthritis, diabetes mellitus, psoriasis, multiple sclerosis, uvietis, inflammation of the eye, and graft-versus-host disease (GvHD).

12. A method of treating an HTLV-1-associated myelopathy (HAM)/tropical spastic paraparesis (TSP) associated disease, the method comprising administering the pharmaceutical composition of claim 5 to a subject in need thereof, wherein the HAM/TSP associated disease is selected from the group consisting of Adult T-cell Leukemia (ATL), HTLV-associated Myelopathy/Tropical Spastic Paraparesis (HAM/TSP), and other non-neeoplastic inflammatory diseases associated with HTLV such as uveitis (HU), arthropathy, pneumopathy, dermatitis, exocrinopathy, and myositis.

13. A method of treating an inflammatory respiratory disease, the method comprising administering the pharmaceutical composition of claim 5 to a subject in need thereof, wherein the inflammatory respiratory disease is selected from the group consisting of asthma, sinusitis, hay fever, bronchitis, chronic obstructive pulmonary disease (COPD), allergic rhinitis, acute and chronic otitis, and lung fibrosis.

14. A method of treating a cosmetic condition, the method comprising administering the pharmaceutical composition of claim 5 to a subject in need thereof, wherein the cosmetic disease is selected from the group consisting of acne, hair loss, sunburn, nail maintenance, and appearance of aging.

15. A genetic construct comprising:

a nucleotide sequence encoding a composite peptide; and

at least one regulatory element, wherein the at least one regulatory element is configured to regulate an expression of the composite peptide,

wherein the composite peptide, when expressed, can inhibit the activity of two or more γc-cytokines selected from the group consisting of IL-2, IL-4, IL-7, IL-9, IL-15, and IL-21;

wherein the composite peptide comprises an amino acid sequence Xaa Phe Leu Xaa Xaa Xaa Xaa Xaa Xaa Xaa Gln (SEQ ID NO: 2), wherein the Xaa at position 1 is D or E, the Xaa at position 4 is E, Q, or N, the Xaa at position 5 is S or R, the Xaa at position 6 is any amino acid, the Xaa at position 7 is I or K, the Xaa at position 8 is any amino acid, the Xaa at position 9 is L or I, the Xaa at position 10 is any amino acid.

16. The genetic construct of claim 15 , wherein the genetic construct is a DNA.

17. The genetic construct of claim 15 , wherein the genetic construct is an RNA.

18. The genetic construct of claim 15 , wherein the composite peptide comprises the amino acid sequence I-K-E-F-L-Q-R-F-I-H-I-V-Q-S-I-I-N-T-S(SEQ ID NO: 1) (BNZ-γ).

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 6, 2023
From: TAGAYA, YUTAKA; AZIMI, NAZLI
To: BIONIZ, LLC
Reel/Frame 065148/0010 →
MERGER AND CHANGE OF NAME Recorded Oct 6, 2023
From: BIONIZ, LLC; BIONIZ THERAPEUTICS, INC.
To: BIONIZ THERAPEUTICS, INC.
Reel/Frame 065153/0383 →
Continuity (9)
Continuation 15474312 · Mar 30, 2017
Continuation 14852240 · Sep 11, 2015
Continuation 13980305 · Jul 17, 2013
Continuation 13868725 · Apr 23, 2013
Continuation 13589017
Continuation PCTUS2012021566 · Jan 17, 2012
Provisional Application 61527049 · Aug 24, 2011
Provisional Application 61433890 · Jan 18, 2011
Related Publication 20190194255A1 · Jun 27, 2019
Cited By (1)
US 12,600,757