IP Library Granted Patent US 8,273,356
Granted Patent B2
US 8,273,356 · App. 12/624,566 · Granted Sep 25, 2012

Anti-IgE vaccines

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Quick Facts
Patent No.
US 8,273,356
App. No.
12/624,566
Granted
Sep 25, 2012
Kind
B2
Abstract

The present invention provides compositions and methods for the use of antigenic peptides derived from the Fc portion of the epsilon heavy chain of an IgE molecule as vaccines for the treatment and prevention of IgE-mediated allergic disorders. In particular, the invention provides compositions, methods for the treatment and prevention of IgE-mediated allergic disorders comprising an immunogenic amount of one or more antigenic peptides derived from the CH3 domain or junction of Ch-3/CH4 domain of an IgE molecule and methods for the evaluation of IgE mediated allergies in dogs.

Claims (10)

1. A pharmaceutical composition comprising an immunogenically effective amount of one or more isolated antigenic fusion proteins consisting of the amino acid sequence of SEQ ID NO: 11 and a heterologous carrier protein, wherein said fusion protein induces a non-anaphylactic anti-IgE immune response when administered to an animal.

2. The pharmaceutical composition of claim 1 further comprising one or more pharmaceutical carriers.

3. The pharmaceutical composition according to claim 1 or 2 further comprising an adjuvant.

4. The pharmaceutical composition according to claim 1 or 2 for the treatment of IgE-mediated allergic disorders.

5. The pharmaceutical composition of claim 3 for the treatment of IgE-mediated allergic disorders.

6. The pharmaceutical composition of claim 4 , wherein the IgE-mediated allergic disorder is selected from the group consisting of asthma, allergic rhinitis, gastrointestinal allergies, food allergies, eosinophilia, conjunctivitis, glomerular nephritis and graft-versus-host disease.

7. The pharmaceutical composition of claim 5 , wherein the IgE-mediated allergic disorder is selected from the group consisting of asthma, allergic rhinitis, gastrointestinal allergies, food allergies, eosinophilia, conjunctivitis, glomerular nephritis and graft-versus-host disease.

8. A polynucleotide sequence encoding the antigenic fusion protein of claim 1 .

9. A host cell containing an expression vector that includes the polynucleotide sequence according to claim 8 .

10. A method for producing an antigenic fusion protein according to claim 1 comprising growing a culture of the host cell of claim 9 in a suitable culture medium, and purifying antigenic fusion protein from the culture.

Assignments (2)
CHANGE OF NAME Recorded Mar 28, 2013
From: AH USA 42 LLC
To: ZOETIS LLC
Reel/Frame 030119/0866 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 11, 2013
From: PFIZER INC.
To: AH USA 42 LLC
Reel/Frame 029609/0336 →