IP Library Granted Patent US 7,622,107
Granted Patent B2
US 7,622,107 · App. 10/595,385 · Granted Nov 24, 2009

Recombinant intracellular pathogen immunogenic compositions and methods for use

Assignee: The Regents of the University of California
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Quick Facts
Patent No.
US 7,622,107
App. No.
10/595,385
Granted
Nov 24, 2009
Kind
B2
Abstract

Immunogenic compositions comprising recombinant attenuated intracellular pathogens that have been transformed to express recombinant immunogenic antigens of the same or other intracellular pathogens are provided. Exemplary immunogenic compositions include, but are not limited to attenuated recombinant Mycobacteria expressing the major extracellular non-fusion proteins of Mycobacteria and/or other intracellular pathogens. Other embodiments are provided wherein the recombinant attenuated intracellular pathogen is auxotrophic.

Claims (20)

1. A prime-boost vaccine strategy for protecting a mammal against infection by a pathogen of the genus Mycobacterium comprising:

administering a first priming immunogenic composition to a vaccinee wherein said first priming immunogenic composition is a Bacille Calmette Guèrin (BCG); and

administering a second boosting immunogenic composition, after the passage of a period of time, to said vaccinee optionally in the presence of an adjuvant, wherein said second boosting immunogenic composition comprises at least one purified Mycobacteria major extracellular protein selected from the group consisting of Mycobacterium tuberculosis (Mtb) 23.5 kDa protein, Mtb 30 kDa protein (Ag85B), Mycobacterium bovis (MB) 30 kDa protein, Mycobacterium leprae (ML) 23.5 kDa protein, and ML 30 kDa protein;

wherein a protective immune response against said pathogen of the genus Mycobacterium is produced in said vaccinee.

2. The prime-boost vaccine strategy according to claim 1 wherein said BCG is a recombinant BCG (rBCG) that over expresses at least one Mycobacteria major extracellular protein.

3. The prime-boost vaccine strategy according to claim 1 wherein said pathogen of the genus Mycobacterium is selected from the group consisting of Mycobacterium tuberculosis (Mtb), Mycobacterium bovis (MB), and Mycobacterium leprae (ML).

4. The prime-boost vaccine strategy according to claim 1 wherein said purified Mycobacteria major extracellular protein is a purified recombinant Mycobacteria major extracellular protein.

5. The prime-boost vaccine strategy according to claim 2 wherein said rBCG over expresses at least one Mycobacteria major extracellular protein selected from the group consisting of Mtb 23.5 kDa protein, Mtb 30 kDa protein, Mtb 32A kDa protein, MB 30 kDa protein, MB 32A kDa protein, ML 23.5 kDa protein, ML 30 kDa protein and ML 32A kDa protein.

6. The prime-boost vaccine strategy according to claim 2 wherein said Mycobacteria major extracellular protein and said purified Mycobacteria major extracellular protein are the same protein.

7. A prime-boost vaccine strategy for protecting a mammal against infection by a pathogen of the genus Mycobacterium comprising:

administering a first priming immunogenic composition to a vaccinee wherein said first immunogenic priming composition is BCG; and

administering a second boosting immunogenic composition, after the passage of a period of time, to said vaccinee wherein said second boosting immunogenic composition is purified Mycobacterium tuberculosis 30 kDa protein (Ag85B);

wherein a protective immune response against said pathogen of the genus Mycobacterium is produced in said vaccinee.

8. The prime-boost vaccine strategy according to claim 7 further comprising an adjuvant.

9. The prime-boost vaccine strategy according to claim 7 wherein said BCG is a rBCG that over expresses at least one Mycobacteria major extracellular protein.

10. The prime-boost vaccine strategy according to claim 7 wherein said pathogen of the genus Mycobacterium is selected from the group consisting of M. tuberculosis , M. bovis , and M. leprae.

11. A prime-boost vaccine strategy for protecting against infection by a pathogen of the genus Mycobacterium comprising:

identifying an individual who has previously been immunized with BCG; and

administering to said individual a boosting immunogenic composition, optionally in the presence of an adjuvant, wherein said boosting immunogenic composition comprises at least one purified Mycobacteria major extracellular protein selected from the group consisting of Mtb 23.5 kDa protein, Mtb 30 kDa protein (Aq85B), MB 30 kDa protein, ML 23.5 kDa protein, and ML 30 kDa protein;

wherein a protective immune response against said pathogen of the genus Mycobacterium is produced in said individual.

Assignments (2)
CONFIRMATORY LICENSE Recorded Mar 3, 2009
From: UNIVERSITY OF CALIFORNIA LOS ANGELES
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 022334/0701 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 18, 2008
From: HORWITZ, MARCUS A.; HARTH, GUNTER; TULLIUS, MICHAEL V.
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 021848/0472 →
Continuity (2)
Provisional Application 6051256500 · Oct 16, 2003
Related Publication 20070128216A1 · Jun 7, 2007