IP Library Granted Patent US 7,208,289
Granted Patent B2
US 7,208,289 · App. 11/027,949 · Granted Apr 24, 2007

Methods of identifying compounds that modulate IL-4 receptor mediated IgE synthesis utilizing a CLLD8 protein

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Quick Facts
Patent No.
US 7,208,289
App. No.
11/027,949
Granted
Apr 24, 2007
Kind
B2
Abstract

The present provides compounds capable of modulating IL-4 receptor-mediated IgE production, as well as IL-4 induced processes associated therewith, methods and kits for identifying such compounds that utilize a CLLD8 protein as a surrogate analyte and methods of using the compounds in a variety of in vitro, in vitro and ex vivo contexts.

Claims (26)

1. A method of identifying a compound that modulates IL-4 receptor-mediated IgE production-or a process associated with IL-4 receptor-mediated IgE production, comprising determining whether the compound binds a CLLD8 protein, wherein binding to the CLLD8 protein identifies the compound as being an agonist or antagonist of IL-4 induced IgE production-or a process associated with IL-4 receptor-mediated IgE production.

2. The method of claim 1 in which the compound identified is an agonist or antagonist of IL-4 receptor-mediated IgE production.

3. The method of claim 1 in which the compound identified is an agonist or antagonist of IL-4 receptor-mediated isotype switching of B-cells.

4. The method of claim 1 in which the compound identified is an agonist or antagonist of IL-4 induced transcription from a gerinline ε promoter.

5. The method of claim 1 in which the compound is an agonist or antagonist that specifically affects IL-4 induced IgE production but which does not significantly affect production of another Ig isotype.

6. The method of claim 1 in which the CLLD8 protein is a mammalian CLLD8 protein.

7. The method of claim 6 in which the mammalian CLLD8 protein is a human CLLD8 protein.

8. The method of claim 1 in which determining whether the compound binds the CLLD8 protein is done in a competitive binding assay.

9. The method of claim 8 in which the compound competes for binding the CLLD8 protein with an active CL02A3 compound.

10. The method of claim 9 in which the active CL02A3 compound is selected from the group consisting of CL02A3wt (SEQ ID NO:1), CL02A3LG (SEQ ID NO:2), CL02A3GW (SEQ ID NO:3) and an analog thereof.

11. The method of claim 1 which is carried out in a cell-free system with an isolated CLLD8 protein.

12. The method of claim 1 in which the compound is a small organic compound.

13. The method of claim 12 in which the small organic compound has a molecular weight in the range of about 100–2500 dalton.

14. The method of claim 1 in which the compound is selected from the group consisting of peptides and peptide analogs.

15. The method of claim 1 , further including the step of confirming that the identified compound is an agonist or antagonist of IL-4 induced IgE production or a process associated with IL-4 induced IgE production.

16. The method of claim 1 in which the compound is in a pool of candidate compounds.

17. The method of claim 16 which is carried out in the presence of a compound known to bind the CLLD8 protein such that those candidate compounds of the pool that competitively bind the CLLD8 protein are identified.

18. The method of claim 17 in which the compound known to bind the CLLD8 protein is an active CL02A3 compound.

19. The method of claim 18 in which the active CL02A3 compound is selected from the group consisting of CL02A3wt (SEQ ID NO:1), CL02A3LG (SEQ ID NO:2), CL02A3GW (SEQ ID NO:3) and an analog thereof.

20. The method of claim 16 in which the candidate compounds are peptides or small organic compounds.

21. The method of claim 16 in which the pool of candidate compounds is a phage display library.

22. The method of claim 16 in which the candidate compounds are immobilized on a substrate or a plurality of substrates.

23. The method of claim 16 in which the compound or CLLD8 protein is labeled with a detectable label.

24. The method of claim 16 in which the CLLD8 protein is immobilized on a substrate.

25. The method of claim 16 , further including the step of confirming the compounds as agonists or antagonists of IL-4 receptor-mediated IgE production or a process associated with IL-4 induced IgE production.

26. The method according to claim 1 or claim 16 in which the CLLD8 is a polypeptide having the amino acid sequence of SEQ ID NO:18.

Assignments (2)
SECURITY INTEREST Recorded Aug 25, 2022
From: RIGEL PHARMACEUTICALS, INC.
To: MIDCAP FINANCIAL TRUST
Reel/Frame 061327/0712 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 8, 2007
From: MASUDA, ESTEBAN; KINSELLA, TODD M.; WARNER, JUSTIN E.; KINOSHITA, TAISEI; BENNETT, MARK K.; ANDERSON, DAVID C.
To: RIGEL PHARMACEUTICALS, INC.
Reel/Frame 018983/0223 →