IP Library Granted Patent US 7,189,513
Granted Patent B2
US 7,189,513 · App. 10/472,661 · Granted Mar 13, 2007

Human papilloma virus immunoreactive peptides

Assignee: The United States of America as represented by the Department of Health and Human Services
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Quick Facts
Patent No.
US 7,189,513
App. No.
10/472,661
Granted
Mar 13, 2007
Kind
B2
Abstract

This invention provides immunogenic peptides from the HPV-18E6 protein that comprise class I restricted T cell epitopes and discloses methods of administering these peptides to individuals, and a method for monitoring or evaluating an immune response to HPV with these peptides.

Claims (12)

1. A method for inducing an immune response against human papilloma virus 16 (HPV 16) comprising administering to a subject a composition, which is selected from a group consisting of:

(i) a peptide of 20 amino acids or less comprising a cross-reactive peptide from the E6 protein of a related HPV strain, HPV 18, that has higher affinity for the HLA-A2.1 molecule than the corresponding epitope from HPV 16 itself, said peptide consisting of the sequence X 1 KLPDLCTEL(SEQ ID NO:1)X 2 , wherein X 1 and X 2 are peptides of 0–11 amino acids in length comprising contiguous HPV 18 E6 amino acid sequences;

(ii) an antigen presenting cell pulsed with said peptide; and

(iii) a cell sensitized in vitro to said peptide.

2. The method of claim 1 , wherein the composition is in a pharmaceutically acceptable carrier.

3. The method of claim 1 , wherein the composition is in a sterile medium.

4. The method of claim 2 , further comprising co-administering to the subject an immune adjuvant selected from non-specific immune adjuvants, subcellular microbial products and fractions, haptens, immunogenic proteins, immunomodulators, interferons, thymic hormones and colony stimulating factors.

5. The method of claim 1 , wherein the administration comprises sensitizing CD8+ cells in vitro to said peptide and administering the sensitized cells to the subject in a sterile medium.

6. A method for inducing an immune response against human papilloma virus 16 (HPV 16) comprising administering to a subject diagnosed with HPV16 infection a composition, which is selected from a group consisting of:

(i) a peptide of 20 amino acids or less comprising a cross-reactive peptide from the E6 protein of a related HPV strain, HPV 18, that has higher affinity for the HLA-A2.1 molecule than the corresponding epitope from HPV 16 itself, said peptide consisting of the sequence X 1 KLPDLCTEL(SEQ ID NO:1)X 2 , wherein X 1 and X 2 are peptides of 0–11 amino acids in length comprising contiguous HPV 18 E6 amino acid sequences;

(ii) an antigen presenting cell pulsed with said peptide; and

(iii) a cell sensitized in vitro to said peptide.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 27, 2004
From: KHLEIF, SAMIR N.; BERZOFSKY, JAY A.
To: HEALTH AND HUMAN SERVICES, THE, UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY
Reel/Frame 014907/0929 →
Continuity (2)
Provisional Application 6027852000 · Mar 23, 2001
Related Publication 20040106551A1 · Jun 3, 2004