IP Library Granted Patent US 10,793,613
Granted Patent B2
US 10,793,613 · App. 15/536,580 · Granted Oct 6, 2020

Compositions and methods for targeted cytokine delivery

Inventors: Alexander Sasha Krupnick (St. Louis, MO); Eric Reed Lazear (St. Louis, MO); Daved Henry Fremont (St. Louis, MO)
C07K14/55A61K47/642A61K47/65C07K14/005A61K38/00C07K2299/00C07K2319/20C07K2319/33C12N2710/24122Y02A50/393
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Quick Facts
Patent No.
US 10,793,613
App. No.
15/536,580
Granted
Oct 6, 2020
Kind
B2
Abstract

The present disclosure encompasses compositions and methods for targeted cytokine delivery. The compositions disclosed herein comprise a cytokine linked to a ligand and may improve immunotherapy by limiting side effects associated with immunotherapy.

Claims (9)

1. A composition comprising a chimeric peptide, the chimeric peptide comprising an orthopoxvirus major histocompatibility complex class 1-like protein (OMCP) peptide linked to an IL2 peptide, wherein the OMCP peptide comprises the amino acid sequence of SEQ ID NO: 7, and the IL2 peptide comprises the amino acid sequence of SEQ ID NO: 5 or SEQ ID NO: 5 with at least one mutation, wherein said at least one mutation is selected from the group consisting of R38A, F42K, and C125S.

2. A composition comprising a chimeric peptide, the chimeric peptide comprising an orthopoxvirus major histocompatibility complex class 1-like protein (OMCP) peptide linked to an IL2 peptide, wherein the OMCP peptide comprises the amino acid sequence of SEQ ID NO: 13, and the IL2 peptide comprises the amino acid sequence of SEQ ID NO: 5 or SEQ ID NO: [6]5 with at least one mutation, wherein said at least one mutation is selected from the group consisting of R38A, F42K, and C125S.

3. A composition comprising a chimeric peptide, the chimeric peptide comprising an orthopoxvirus major histocompatibility complex class 1-like protein (OMCP) peptide linked to an IL2 peptide, wherein the OMCP peptide comprises the amino acid sequence of SEQ ID NO: 14, and the IL2 peptide comprises the amino acid sequence of SEQ ID NO: 5 or SEQ ID NO: 5 with at least one mutation, wherein said at least one mutation is selected from the group consisting of R38A, F42K, and C125S.

4. The composition of claim 1 , wherein the IL2 peptide comprises the amino acid sequence of SEQ ID NO: 5.

5. The composition of claim 2 , wherein the IL2 peptide comprises the amino acid sequence of SEQ ID NO: 5.

6. The composition of claim 3 , wherein the IL2 peptide comprises the amino acid sequence of SEQ ID NO: 5.

7. The composition of claim 1 , wherein the IL2 peptide comprises the amino acid sequence of SEQ ID NO: 5 with the at least one mutation selected from the group consisting of R38A, F42K, and C125S.

8. The composition of claim 2 , wherein the IL2 peptide comprises the amino acid sequence of SEQ ID NO: 5 with the at least one mutation selected from the group consisting of R38A, F42K, and C125S.

9. The composition of claim 3 , wherein the IL2 peptide comprises the amino acid sequence of SEQ ID NO: 5 with the at least one mutation selected from the group consisting of R38A, F42K, and C125S.

Assignments (2)
CONFIRMATORY LICENSE Recorded Jan 29, 2019
From: WASHINGTON UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 048180/0294 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 31, 2017
From: KRUPNICK, ALEXANDER S.; FREMONT, DAVED H.; LAZEAR, ERIC R.
To: WASHINGTON UNIVERSITY
Reel/Frame 043142/0065 →
Continuity (3)
Provisional Application 62091898 · Dec 15, 2014
Provisional Application 62243829 · Oct 20, 2015
Related Publication 20190092831A1 · Mar 28, 2019