T cell receptors
US-2019144521-A1 · May 16, 2019 · US
US11786583B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11786583-B2 |
| Application number | US-202117245918-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 30, 2021 |
| Priority date | Dec 23, 2014 |
| Publication date | Oct 17, 2023 |
| Grant date | Oct 17, 2023 |
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.
A peptide consists of the amino acid sequence KLSPTVVGL (SEQ ID NO: 6) in the form of a pharmaceutically acceptable salt, in which the peptide has the ability to bind to an MHC class-I molecule and, when bound to MHC, is capable of being recognized by CD8 T cells. A composition contains a peptide consisting of the amino acid sequence KLSPTVVGL (SEQ ID NO: 6), an adjuvant, and a pharmaceutically acceptable carrier.
Opening claim text (preview).
The invention claimed is: 1. A peptide consisting of the amino acid sequence KLSPTVVGL (SEQ ID NO: 6) in the form of a pharmaceutically acceptable salt. 2. The peptide of claim 1 , wherein said peptide has the ability to bind to a major histocompatibility complex (MHC) class-I molecule, and wherein said peptide, when bound to said MHC, is capable of being recognized by CD8+ T cells. 3. The peptide of claim 1 , wherein the pharmaceutically acceptable salt is chloride salt. 4. The peptide of claim 1 , wherein the pharmaceutically acceptable salt is acetate salt. 5. The peptide in the form of a pharmaceutically acceptable salt of claim 1 , wherein said peptide is produced by solid phase peptide synthesis or produced by a yeast cell or bacterial cell expression system. 6. A composition comprising the peptide of claim 1 , wherein the composition is a pharmaceutical composition and comprises a buffer. 7. A composition comprising the peptide of claim 1 , wherein the composition comprises an adjuvant and a pharmaceutically acceptable carrier. 8. The composition of claim 7 , wherein the peptide is in the form of a chloride salt. 9. The composition of claim 7 , wherein the peptide is in the form of an acetate salt. 10. The composition of claim 7 wherein the adjuvant is selected from the group consisting of imiquimod, resiquimod, granulocyte-macrophage colony-stimulating factor (GM-CSF), cyclophosphamide, sunitinib, bevacizumab, interferon-alpha, interferon-beta, CpG oligonucleotides, polyinosinic:polycytidylic acid (poly-(I:C)), RNA, sildenafil, particulate formulations with poly(lactide co-glycolide) (PLG), virosomes, interleukin (IL)-1, IL-2, IL-4, IL-7, IL-12, IL-13, IL-15, IL-21, and IL-23. 11. The composition of claim 10 , wherein the adjuvant is IL-2. 12. The composition of claim 10 , wherein the adjuvant is IL-7. 13. The composition of claim 10 , wherein the adjuvant is IL-12. 14. The composition of claim 10 , wherein the adjuvant is IL-15. 15. The composition of claim 10 , wherein the adjuvant is IL-21. 16. A pegylated peptide consisting of the amino acid sequence of KLSPTVVGL (SEQ ID NO: 6) or a pharmaceutically acceptable salt thereof, wherein the peptide is cross-linked with a polyethylene glycol (PEG). 17. The peptide of claim 16 , wherein the pharmaceutically acceptable salt is chloride salt. 18. The peptide of claim 16 , wherein the pharmaceutically acceptable salt is acetate salt. 19. A composition comprising the pegylated peptide of claim 16 or pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier. 20. A peptide consisting of the amino acid sequence of KLSPTVVGL (SEQ ID NO: 6), wherein at least one amino acid of the peptide is a D-amino acid.
Antigen-pulsed cells, e.g. T-cells · CPC title
Antigen presenting cells [APCs], e.g. dendritic cells or macrophages · CPC title
Aptamers, i.e. nucleic acids binding a target molecule specifically and with high affinity without hybridising therewith {; Nucleic acids binding to non-nucleic acids, e.g. aptamers} · CPC title
T lymphocytes · CPC title
Lymphocytes; B-cells; T-cells; Natural killer cells; Interferon-activated or cytokine-activated lymphocytes (when activated by a specific antigen A61K39/00) · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.