IP Library Granted Patent US 7,993,651
Granted Patent B2
US 7,993,651 · App. 10/168,843 · Granted Aug 9, 2011

Chimeric human immunodeficiency virus (HIV) immunogens comprising GAG P24-P17 fused to multiple cytotoxic T lymphocyte (CTL) epitopes

Assignees: Medical Research Council; International AIDS Vaccine Initiative; University of Nairobi
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Quick Facts
Patent No.
US 7,993,651
App. No.
10/168,843
Granted
Aug 9, 2011
Kind
B2
Abstract

Disclosed is an immunogen in sterile form suitable for administration to a human subject, the immunogen comprising: at least a portion of the gag protein of HIV, said gag protein being from an HIV clade or having a consensus sequence for one or more HIV clades, and comprising at least parts of p17 and p24; and a synthetic polypeptide comprising a plurality of amino acid sequences, each sequence comprising a human CTL epitope of an HIV protein, and wherein a plurality of HIV proteins are represented in the synthetic polypeptide, said CTL epitopes being selected to stimulate an immune response to one or more HIV clades of interest.

Claims (20)

1. An immunogen comprising the amino acid sequence shown in FIG. 1B .

2. A polypeptide comprising the amino acid sequence shown in FIG. 8A .

3. An immunogen in sterile form suitable for administration to a human subject, the immunogen comprising one of the following structures:

(a) NH2-p24-p17-CTL polyepitope-COOH;

(b) NH2-p24-p17-tat-CTL polyepitope-COOH;

(c) NH2-p24-p17-CTL polyepitope-tat-COOH; or

(d) NH2-p24-p17-C pol-rev-tat-nef-N pol-CTL polyepitope-COOH;

wherein the CTL polyepitope comprises at least 10 of the human CTL epitopes identified in Table 1.

4. An immunogen according to claim 3 , in which p17 is modified to prevent N-terminal myristylation.

5. An immunogen according to claim 3 , in which at least some of the human CTL epitopes present in the synthetic polypeptide are overlapping.

6. An immunogen according to claim 3 , in which at least 50% of the human CTL epitopes present in the synthetic polypeptide are overlapping.

7. An immunogen according to claim 3 , in which at least some of the human CTL epitopes present in the synthetic polypeptide are adjacent.

8. An immunogen in according to claim 3 , in which at least some of the human CTL epitopes are separated by non-epitopic amino acid sequences.

9. An immunogen according to claim 3 , comprising at least one epitope which is recognized by one or more laboratory test mammals.

10. An immunogen according to claim 9 , wherein said epitope recognized by one or more laboratory test mammals is a CTL epitope.

11. An immunogen according to claim 3 , in which the synthetic polypeptide comprises at least 15 of the human CTL epitopes identified in Table 1.

12. An immunogen according to claim 3 , in which the synthetic polypeptide comprises at least 20 of the human CTL epitopes identified in Table 1.

13. An immunogen according to claim 3 , in which the synthetic polypeptide comprises at least 23 of the human CTL epitopes identified in Table 1.

14. A bacterium comprising an immunogen in accordance with claim 3 .

15. The bacterium according to claim 14 which is an attenuated pathogen suitable for administration to a human subject.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 24, 2002
From: HANKE, TOMAS; MCMICHAEL, ANDREW JAMES
To: MEDICAL RESEARCH COUNCIL OF UNITED KINGDOM; INTERNATIONAL AIDS VACCINE INITIATIVE; NAIROBI, UNIVERSITY OF
Reel/Frame 013425/0207 →
Priority Claims (2)
GB 9930294.5 · Dec 23, 1999 · national
GB 0025234.6 · Oct 14, 2000 · national
Continuity (1)
Related Publication 20030108562A1 · Jun 12, 2003