NZ779550B2 - Multivalent pd-l1 binding compounds for treating cancer - Google Patents
Multivalent pd-l1 binding compounds for treating cancer Download PDFInfo
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- NZ779550B2 NZ779550B2 NZ779550A NZ77955020A NZ779550B2 NZ 779550 B2 NZ779550 B2 NZ 779550B2 NZ 779550 A NZ779550 A NZ 779550A NZ 77955020 A NZ77955020 A NZ 77955020A NZ 779550 B2 NZ779550 B2 NZ 779550B2
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- Prior art keywords
- polypeptide
- multivalent
- cell death
- ligand
- programmed cell
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/005—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from viruses
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- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/705—Receptors; Cell surface antigens; Cell surface determinants
- C07K14/70503—Immunoglobulin superfamily
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- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/705—Receptors; Cell surface antigens; Cell surface determinants
- C07K14/70503—Immunoglobulin superfamily
- C07K14/70521—CD28, CD152
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- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2319/00—Fusion polypeptide
- C07K2319/30—Non-immunoglobulin-derived peptide or protein having an immunoglobulin constant or Fc region, or a fragment thereof, attached thereto
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- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
- C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
- C12N15/85—Vectors or expression systems specially adapted for eukaryotic hosts for animal cells
- C12N15/86—Viral vectors
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- C12N2710/00—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA dsDNA viruses
- C12N2710/00011—Details
- C12N2710/10011—Adenoviridae
- C12N2710/10022—New viral proteins or individual genes, new structural or functional aspects of known viral proteins or genes
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- C12N2710/00—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA dsDNA viruses
- C12N2710/00011—Details
- C12N2710/10011—Adenoviridae
- C12N2710/10311—Mastadenovirus, e.g. human or simian adenoviruses
- C12N2710/10322—New viral proteins or individual genes, new structural or functional aspects of known viral proteins or genes
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- C12N2710/00011—Details
- C12N2710/10011—Adenoviridae
- C12N2710/10311—Mastadenovirus, e.g. human or simian adenoviruses
- C12N2710/10341—Use of virus, viral particle or viral elements as a vector
- C12N2710/10343—Use of virus, viral particle or viral elements as a vector viral genome or elements thereof as genetic vector
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- C12N2710/00—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA dsDNA viruses
- C12N2710/00011—Details
- C12N2710/10011—Adenoviridae
- C12N2710/10311—Mastadenovirus, e.g. human or simian adenoviruses
- C12N2710/10341—Use of virus, viral particle or viral elements as a vector
- C12N2710/10345—Special targeting system for viral vectors
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- C12N2830/00—Vector systems having a special element relevant for transcription
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- C12N7/00—Viruses; Bacteriophages; Compositions thereof; Preparation or purification thereof
Abstract
This invention provides methods and materials for treating cancer. The invention encompasses methods and materials for delivering programmed death-ligand 1 (PD-L1) binding compounds and/or compositions containing one or more monovalent or multivalent programmed death-ligand 1 (PD-L1) binding compounds which are administered to a mammal having cancer to treat the mammal. In some cases, a multivalent PD-L1 binding compound can include two or more programmed cell death protein 1 (PD-1) polypeptides (and/or fragments thereof having the ability to bind PD-L1). This invention also provides methods and materials for making multivalent PD-L1 binding compounds and methods and materials for making nucleic acid molecules that encode PD-L1 binding compounds.
Claims (12)
1. A multivalent programmed cell death protein ligand 1 (PD-L1) binding compound, comprising a plurality of amino acid chains, wherein each amino acid chain comprises at least one programmed cell death n 1 (PD-1) polypeptide, wherein each amino acid chain sing at least one programmed cell death protein 1 (PD-1) polypeptide is associated with a recombinant Adenovirus (Ad) and the plurality of amino acid chains are present on a coat polypeptide of the recombinant Ad, and n the recombinant Ad comprises capsid hexon polypeptides of an Ad strain Ad6 and at least one capsid hexon hypervariable region (HVR) polypeptide from Ad strain Ad57.
2. The multivalent programmed cell death protein ligand 1 (PD-L1) binding nd of claim 1, wherein the capsid hexon polypeptides of an Ad strain Ad6 comprise HVR polypeptides 1-7 from Ad strain Ad57.
3. The multivalent programmed cell death protein ligand 1 (PD-L1) binding compound of claim 1, n the capsid hexon polypeptides of an Ad strain Ad6 comprise HVR polypeptides 2-6 from Ad strain Ad57.
4. The multivalent programmed cell death protein ligand 1 (PD-L1) binding compound of any one of claims 1 to 3, wherein the programmed cell death protein 1 (PD-1) polypeptide is a human PD-1 or a murine PD-1.
5. The multivalent programmed cell death protein ligand 1 (PD-L1) g compound of any one of claims 1 to 4, wherein the recombinant Ad is r modified to se heterologous polypeptides selected from targeting polypeptides, therapeutic polypeptides and antigens.
6. The multivalent mmed cell death protein ligand 1 (PD-L1) binding compound of claim 5, wherein the targeting polypeptide is selected from a measles virus lutinin (MVH) polypeptide, a measles virus fusion (MVF) polypeptide, and a vesicular stomatitis virus glycoprotein (VSVG) polypeptide.
7. The multivalent programmed cell death protein ligand 1 (PD-L1) binding compound of claim 5, wherein the therapeutic polypeptide is selected from a 4-1BB ligand (4-1BBL) polypeptide, a OX40 ligand ) ptide, a CD40 ligand (CD40L) polypeptide, and a granulocyte-macrophage colony-stimulating factor (GMCSF ) polypeptide.
8. The multivalent programmed cell death protein ligand 1 ) binding compound of any one of claims 1 to 7, wherein the PD-1 polypeptide is fused to a n K-dependent gamma-carboxyglutamic domain of a factor X single-chain antibody polypeptide (a GLA domain of an FX polypeptide).
9. The multivalent programmed cell death protein ligand 1 ) binding compound of any one of claims 1 to 8, wherein each amino acid chain comprises a targeting molecule selected from a measles virus hemagglutinin (MVH) polypeptide, a measles virus fusion (MVF) ptide, and a vesicular stomatitis virus glycoprotein (VSVG) polypeptide.
10. The multivalent programmed cell death protein ligand 1 (PD-L1) binding compound of claims 1 to 9, wherein each amino acid chain comprises one or more therapeutic polypeptides selected from a 4-1BB ligand (4-1BBL) polypeptide, a OX40 ligand (OX40L) polypeptide, a CD40 ligand (CD40L) polypeptide, and a granulocytemacrophage colony-stimulating factor (GM-CSF) polypeptide.
11. A ceutical composition comprising the multivalent programmed cell death protein ligand 1 (PD-L1) binding compound of any one of claims 1 to 10 and a pharmaceutically acceptable carrier.
12. Use of a nd or pharmaceutical composition as claimed in any one of claims 1 to 11 in the preparation of a medicament for use in treating cancer in a subject in need thereof.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201962839916P | 2019-04-29 | 2019-04-29 | |
| PCT/US2020/030240 WO2020223217A1 (en) | 2019-04-29 | 2020-04-28 | Multivalent pd-l1 binding compounds for treating cancer |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NZ779550A NZ779550A (en) | 2024-08-30 |
| NZ779550B2 true NZ779550B2 (en) | 2024-12-03 |
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