IP Library Granted Patent US 7,517,861
Granted Patent B2
US 7,517,861 · App. 10/888,785 · Granted Apr 14, 2009

Immunostimulatory nucleic acid molecules

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Quick Facts
Patent No.
US 7,517,861
App. No.
10/888,785
Granted
Apr 14, 2009
Kind
B2
Abstract

Nucleic acids containing unmethylated CpG dinucleotides and therapeutic utilities based on their ability to stimulate an immune response and to redirect a Th2 response to a Th1 response in a subject are disclosed. Methods for treating atopic diseases, including atopic dermatitis, are disclosed.

Claims (12)

1. A method of decreasing IgE in a subject who has been exposed to an allergen comprising administering to the subject an immunostimulatory oligonucleotide/delivery complex, said delivery complex comprising an oligonucleotide linked to a biodegradable delivery complex, wherein the oligonucleotide comprises the sequence 5′-C, G-3′, wherein the immunostimulatory oligonucleotide is 8 to 40 nucleotides in length and comprises: 5′ X 1 X 2 CGX 3 X 4 3′, wherein C and G are unmethylated and X 1 , X 2 , X 3 , and X 4 are nucleotides, in an amount sufficient to decrease IgE in the subject, wherein the decrease in IgE is relative to that observed in the subject who has been exposed to an allergen but is not treated with an immunostimulatory oligonucleotide/delivery complex.

2. The method of claim 1 , wherein said complex is antigen-free.

3. The method of claim 1 , wherein said complex further comprises an antigen.

4. The method of claim 1 , wherein said delivery complex is a liquid phase microcarrier.

5. The method of claim 1 , wherein said immunostimulatory oligonucleotide is covalently linked to said delivery complex.

6. The method of claim 1 , wherein said immunostimulatory oligonucleotide is non-covalently linked to said delivery complex.

7. The method of claim 1 , wherein said immunostimulatory oligonucleotide comprises a phosphate backbone modification.

8. The method of claim 7 , wherein said phosphate backbone modification is a phosphorothioate.

9. The method of claim 1 , wherein the immunostimulatory oligonucleotide does not include a GCG trinucleotide at a 5′ and/or 3′ terminal.

10. The method of claim 1 wherein the immunostimulatory oligonucleotide does not contain a 5′X 1 X 2 CGX 3 X 4 3′ palindrome.

11. The method of claim 1 , wherein said oligonucleotide comprises the sequence 5′-T, C, G-3′.

12. The method of claim 1 , wherein the individual has a viral infection.

Assignments (6)
CONFIRMATORY LICENSE Recorded Oct 13, 2008
From: UNIVERSITY OF IOWA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 021703/0237 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 13, 2005
From: CPG IMMUNOPHARMACEUTICALS, INC.
To: COLEY PHARACEUTICAL GROUP, INC.
Reel/Frame 015590/0310 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 13, 2005
From: KRIEG, ARTHUR M.
To: IOWA RESEARCH FOUNDATION, THE UNIVERSITY OF
Reel/Frame 015590/0470 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 13, 2005
From: STEINBERG, ALFRED D.
To: CPG IMMUNOPHARMACEUTICALS INC.
Reel/Frame 015590/0488 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 13, 2005
From: KLINMAN, DENNIS
To: THE UNITED STATES OF AMERICA, AS REPRESENTED BY
Reel/Frame 015590/0505 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 13, 2005
From: KLINE, JOEL
To: UNIVERSITY OF IOWA RESEARCH FOUNDATION, THE
Reel/Frame 015590/0922 →