Methods and nucleic acid molecules for aav vector selection
US-2024417717-A1 · Dec 19, 2024 · US
US9650423B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9650423-B2 |
| Application number | US-201514832060-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 21, 2015 |
| Priority date | Dec 8, 2000 |
| Publication date | May 16, 2017 |
| Grant date | May 16, 2017 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
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.
Opening claim text (preview).
The invention claimed is: 1. An immunogenic composition comprising a peptide having a length of 22 to 45 amino acids that comprises a T helper cell epitope consisting of residues 127-142 of the E6 protein of a type 16 human papilloma virus (HPV), and an adjuvant. 2. The immunogenic composition of claim 1 , wherein the peptide has a length of 22-40 amino acids. 3. The immunogenic composition of claim 1 , wherein the peptide has a length of 22-35 amino acids. 4. The immunogenic composition of claim 1 , wherein the peptide has a length of 32-35 amino acids. 5. The immunogenic composition of claim 1 , wherein the peptide consists of the HPV16 E6 protein segment consisting of residues 109-143, 121-142, 124-158 or 127-158 of HPV 16 E6. 6. The immunogenic composition of claim 1 , wherein the peptide consists of the HPV16 E6 protein segment consisting of residues 127-158 of HPV 16 E6. 7. The immunogenic composition according claim 1 , further comprising a peptide comprising a fragment of HPV 16 E2 protein comprising residues 46-75, 51-70, 61-76, 311-325, 316-330, 346-355 or 351-365 of HPV16 E2. 8. The immunogenic composition according claim 1 , further comprising a peptide comprising a fragment of HPV 16 E7 protein comprising residues 35-77, 35-50, 50-62 or 43-77 of HPV 16 E7. 9. The immunogenic composition according to claim 1 , wherein the adjuvant is selected from the group consisting of (a) an exosome, (b) poly L:C, (c) poly l:poly C12U (d) monophosphoryl lipid A, (e) a CpG-containing nucleic acid, (f) a CD40ligand, and (g) a mixture of any of (a)-(f). 10. The immunogenic composition of claim 9 , wherein the CD40 ligand is an anti-CD40 antibody.
Antibacterial agents · CPC title
Antivirals · CPC title
Liposomes; Vesicles, e.g. nanoparticles; Spheres, e.g. nanospheres; Polymers · CPC title
New viral proteins or individual genes, new structural or functional aspects of known viral proteins or genes · CPC title
Medicinal preparations containing peptides (peptides containing beta-lactam rings A61K31/00; cyclic dipeptides not having in their molecule any other peptide link than those which form their ring, e.g. piperazine-2,5-diones, A61K31/00; ergot alkaloids of the cyclic peptide type A61K31/48; containing macromolecular compounds having statistically distributed amino acid units A61K31/74; medicinal preparations containing antigens or antibodies A61K39/00; medicinal preparations characterised by the non-active ingredients, e.g. peptides as drug carriers, A61K47/00) · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.