IP Library Granted Patent US 7,910,113
Granted Patent B2
US 7,910,113 · App. 12/294,380 · Granted Mar 22, 2011

Tolerizing agents

Assignees: Montana State University; UAB Research Foundation
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Quick Facts
Patent No.
US 7,910,113
App. No.
12/294,380
Granted
Mar 22, 2011
Kind
B2
Abstract

Described herein is the development of fusion proteins useful for inducing tolerance in a subject. In particular embodiments, the tolerizing agents are useful for influence autoimmune, inflammatory, and/or allergic reactions. Example tolerizing fusion proteins contain a targeting portion (which delivers the fusion protein) and a toleragen or allergen or other antigen to which tolerance is desired in a subject. In particular examples, it is demonstrated that a pσ1 fusion protein, when administered orally, facilitates systemic and mucosal tolerance. Also described is the nasal delivery of fusion proteins, for instance for restoring immunogenicity.

Claims (16)

1. A tolerizing fusion protein comprising a targeting portion and an antigen or allergen to which tolerance is desired, wherein the targeting portion comprises a reovirus protein σ1 (pσ1), and wherein administration of the fusion protein to a subject induces tolerance in the subject to the antigen or allergen.

2. The fusion protein of claim 1 , wherein the antigen is an autoantigen or therapeutically active biological.

3. A method to induce tolerance in a subject to an antigen or allergen, comprising administering to the subject the fusion protein of claim 1 .

4. A method of inducing tolerance in a subject to an antigen, comprising:

administering to the subject a single dose of a tolerizing fusion protein, wherein the tolerizing fusion protein comprises (1) a targeting portion comprising a reovirus protein σ1 (pσ1), and (2) the antigen, thereby inducing tolerance in the subject to the antigen.

5. The method of claim 4 , wherein the single dose of the tolerizing fusion protein comprises 1 mg or less of the antigen.

6. The method of claim 5 , wherein the single dose of the tolerizing fusion protein comprises 500 μg or less of the antigen.

7. The method of claim 6 , wherein the single dose of the tolerizing fusion protein comprises 250 μg or less of the antigen.

8. The method of claim 7 , wherein the single dose of the tolerizing fusion protein comprises 100 μg or less of the antigen.

9. A method of inducing antigen specific immune tolerance in a subject, comprising: administering an effective dose of a tolerizing fusion protein comprising a targeting portion and at least one epitope from the antigen to the subject, wherein the tolerizing fusion protein comprises a reovirus protein σ1 (pσ1), thereby inducing tolerance in the subject to the antigen.

10. The method of claim 4 , comprising administering more than one tolerizing fusion protein to the subject.

11. The method of claim 4 , wherein the tolerizing fusion protein is administered orally or nasally.

12. The method of claim 9 , comprising administering more than one tolerizing fusion protein to the subject.

13. The method of claim 9 , wherein the tolerizing fusion protein is administered orally or nasally.

14. The method of claim 3 , comprising administering more than one fusion protein to the subject.

15. The method of claim 3 , wherein the tolerizing fusion protein is administered orally or nasally.

Assignments (2)
CONFIRMATORY LICENSE Recorded Oct 27, 2011
From: MONTANA STATE UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 027130/0568 →
EXECUTIVE ORDER 9424, CONFIRMATORY LICENSE Recorded Mar 13, 2009
From: MONTANA STATE UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 022395/0569 →
Continuity (2)
Provisional Application 60786446 · Mar 27, 2006
Related Publication 20090169578A1 · Jul 2, 2009