Induced activation in dendritic cells
US-2015306140-A1 · Oct 29, 2015 · US
US9572835B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9572835-B2 |
| Application number | US-201514643989-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 10, 2015 |
| Priority date | Feb 18, 2003 |
| Publication date | Feb 21, 2017 |
| Grant date | Feb 21, 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.
The present invention is directed to a composition and method which to treat diseases and to enhance a regulated immune response. More particularly, the present invention is drawn to compositions that are based on dendritic cells modified to express an inducible form of a co-stimulatory polypeptide.
Opening claim text (preview).
What is claimed is: 1. An isolated cell comprising a nucleic acid, wherein the nucleic acid comprises a promoter operably linked to a polynucleotide that encodes a chimeric protein, wherein the chimeric protein comprises a) a membrane targeting region; b) a multimeric ligand binding region; and c) a CD40 polypeptide cytoplasmic region wherein the CD40 polypeptide does not have a functional extracellular domain. 2. The isolated cell of claim 1 , wherein the cell is an antigen presenting cell. 3. The isolated cell of claim 1 , wherein the cell is a dendritic cell. 4. The isolated cell of claim 1 , wherein the membrane targeting region is selected from the group consisting of a myristoylation region, palmitoylation region, prenylation region, and transmembrane sequences of receptors. 5. The isolated cell of claim 1 , wherein the membrane targeting region is a myristoylation region. 6. The isolated cell of claim 1 , wherein the multimeric ligand binding region is selected from the group consisting of FKBP, cyclophilin receptor, the steroid receptor, the tetracycline receptor, heavy chain antibody subunit, light chain antibody subunit, and mutated sequences thereof. 7. The isolated cell of claim 1 , wherein the multimeric ligand binding region comprises an FKBP12 region. 8. The isolated cell of claim 1 , wherein the multimeric ligand binding region comprises FKBP12(V36). 9. The isolated cell of claim 1 , wherein the multimeric ligand binding region comprises tandem copies of an FKBP region. 10. The isolated cell of claim 1 , wherein the multimeric ligand binding region comprises tandem copies of FKBP12(V36). 11. The isolated cell of claim 1 , further comprising a polynucleotide that encodes a tumor antigen. 12. The isolated cell of claim 11 , wherein the tumor antigen is PSMA. 13. A pharmaceutical composition comprising a cell of claim 1 , and a pharmaceutically acceptable buffer.
Immunostimulants · CPC title
Immunoglobulin superfamily (e.g. CD2, CD4, CD8, ICAM molecules, B7 molecules, Fc-receptors, MHC-molecules) · CPC title
viral genome or elements thereof as genetic vector · CPC title
Isomerases (5.) · CPC title
Exopeptidases (3.4.11-3.4.19) · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.