Long peptides of 22-45 amino acid residues that induce and/or enhance antigen specific immune responses

Patent metadata

Field	Value
Publication number	US-10253073-B2
Application number	US-201715581035-A
Country	US
Kind code	B2
Filing date	Apr 28, 2017
Priority date	Dec 8, 2000
Publication date	Apr 9, 2019
Grant date	Apr 9, 2019

Abstract

Epitopes derived from human papilloma virus and peptides having a size of about 22-45 amino acid residues comprising minimal T cell epitopes are disclosed. Also disclosed are clinically relevant approaches for immunizing subjects against (Myco) bacterially and/or virally infected cells or tumor cells. Peptide sequences of 22-35 amino acid residues in length can induce both peptide-specific CD8+ cytolytic cells and CD4+ T-helper cells. Moreover, vaccination with 22-35 residue long peptides results in a more vigorous CD8+ cytolytic T-cell response than vaccination with peptides of the exact minimal CTL epitope length. The intrinsic capacity of certain minimal CTL epitopes which instead of activating cytolytic effector cells tolerize these cytolytic cells, can be overcome by use of these 22-35 amino acid long peptides. Also disclosed are clinically relevant approaches for vaccination and/or treatment of subjects against HPV and methods and uses suited to treat subjects suffering from progressive lesions and/or cervical cancer.

First claim

The invention claimed is:

1. An immunogenic pharmaceutical composition comprising a peptide of 32 to 45 contiguous amino acids of E7 protein of type 16 human papilloma virus (HPV) as a subunit, comprising a T helper cell epitope consisting of residues 35-50 of the HPV type 16 E7 protein and an immune-stimulating amount of a pharmaceutically acceptable adjuvant.

2. The immunogenic composition of claim 1 , wherein the peptide has a length of 32-40 amino acids.

3. The immunogenic composition of claim 1 , wherein the peptide has a length of 32-35 amino acids.

4. The immunogenic composition of claim 1 , wherein the peptide consists of residues 22-56 of HPV 16 E7.

5. The immunogenic composition of claim 1 , further comprising a peptide comprising residues 46-75, 51-70, 61-76, 311-325, 316-330, 346-355 or 351-365 of HPV16 E2.

6. The immunogenic composition of claim 1 , further comprising a peptide comprising residues 50-62 or 43-77 of HPV 16 E7.

7. The immunogenic composition of claim 1 , further comprising a peptide comprising residues 121-142 or 127-140 of HPV 16 E6.

8. The immunogenic composition of claim 1 , wherein the adjuvant is selected from the group consisting of
(a) an exosome,
(b) poly I:C,
(c) poly I:poly C12U,
(d) monophosphoryl lipid A,
(e) a CpG-containing nucleic acid,
(f) a CD40 ligand, and
(g) a mixture of any of (a)-(f).

9. The immunogenic composition of claim 8 , wherein the CD40 ligand is an anti-CD40 antibody.

Assignees

• Academisch Ziekenhuis Leiden

Inventors

• Van Der Burg Sjoerd Hendrikus
• Ottenhoff Tom H M
• Geluk Annemieke
• Schoenmaekers-Welters Maria Johanna Philomena
• De Jong Annemieke M
• Offringa Rienk
• Melief Cornelis Johannes Maria
• Toes Reinaldus Everardus Maria

Classifications

• A61P31/12

  Antivirals · CPC title

• A61P31/04

  Antibacterial agents · CPC title

• A61K2039/57

  characterised by the type of response, e.g. Th1, Th2 · CPC title

• A61K39/12

  Viral antigens · CPC title

• A61K39/04

  Mycobacterium, e.g. Mycobacterium tuberculosis · CPC title