IP Library › Granted Patent US 9,738,696
Granted Patent B2
US 9,738,696 · App. 14/419,873 · Granted Aug 22, 2017

Superkines and synthekines: repurposed cytokines with new and enhanced signaling activities

Inventors: K. Christopher Garcia (Menlo Park, CA); Darren L. Bates (Oak Park, CA); Ignacio Moraga (Don Benito, ES)
Assignee: THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY
C07K14/5406C07K14/52A61K38/00
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Quick Facts
Patent No.
US 9,738,696
App. No.
14/419,873
Granted
Aug 22, 2017
Kind
B2
Abstract

Disclosed herein are IL-4 cytokine compositions with enhanced biological activity having increased selectivity for IL-4 cytokine receptors, and methods for their use. These compositions encompass interleukin-4 (IL-4) muteins. The disclosed methods encompass administering an IL-4 to treat neoplastic diseases, autoimmune diseases, infectious diseases or for expanding a hematopoietic cell population.

Claims (14)

1. A composition comprising an IL-4 mutein, wherein the IL-4 mutein results in higher affinity binding to a shared cytokine receptor relative to a wild-type cytokine, and wherein the IL-4 mutein comprises one or two amino acid substitutions at positions S128 and/or S129, wherein the amino acid numbering is in accordance with wild-type human IL-4 of SEQ ID NO: 4.

2. The composition of claim 1 , wherein the IL-4 mutein results in higher affinity binding to a first shared cytokine receptor relative to a wild-type cytokine and reduced affinity to a second shared cytokine receptor relative to a wild-type cytokine.

3. The composition of claim 2 , wherein the first shared cytokine receptor is expressed at lower levels than the second shared cytokine receptor.

4. The composition of claim 2 , wherein the first shared cytokine receptor is expressed at higher levels than the second shared cytokine receptor.

5. The composition of claim 2 , wherein the reduction in affinity is at least 5-fold.

6. The composition of claim 2 , wherein the first shared cytokine receptor is γc and the second shared cytokine receptor is IL-13Rα1.

7. The composition of claim 2 , wherein the first shared cytokine receptor is IL-13Rα1 and the second shared cytokine receptor is γc.

8. The composition of claim 2 , wherein the first and second shared cytokine receptors are γc and IL-13Rα1.

9. The composition of claim 1 , wherein the IL-4 mutein results in higher affinity binding to a first and a second shared cytokine receptor relative to a wild-type cytokine.

10. The composition of claim 1 , wherein the increase in affinity is at least 10-fold.

11. The composition of claim 1 , wherein the shared cytokine receptor is common γ chain (γc) or interleukin-13 receptor alpha 1 (IL-13Rα1).

12. The composition of claim 1 , wherein the IL-4 mutein further comprises one or more amino acid substitutions at positions selected from the group consisting of: K117, T118, R121, E122, Y124, and S125 wherein the amino acid numbering is in accordance with wild-type human IL-4 of SEQ ID NO: 4.

13. The composition of claim 12 , wherein the IL-4 mutein comprises one or more amino acid substitutions selected from the group consisting of: K117R, T118V, R121Q, E122S, Y124W, S125F, S128G, and S129A, wherein the amino acid numbering is in accordance with wild-type human IL-4 of SEQ ID NO: 4.

14. The composition of claim 12 , wherein the IL-4 mutein comprises the following amino acid substitutions: K117R, T118V, R121Q, E122S, Y124W, S125F, S128G, and S129A, wherein the amino acid numbering is in accordance with wild-type human IL-4 of SEQ ID NO: 4.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 6, 2017
From: GARCIA, K. CHRISTOPHER; BATES, DARREN L; MORAGA, IGNACIO
To: THE BOARD OF TRUSTEES OF THE LELAND STANFOD JUNIOR UNIVERSITY
Reel/Frame 041184/0958 →
Continuity (4)
Provisional Application 61681490 · Aug 9, 2012
Provisional Application 61725791 · Nov 13, 2012
Provisional Application 61825980 · May 21, 2013
Related Publication 20160244499A1 · Aug 25, 2016