Use of FLT3 ligand for enhancing immune responses in RNA immunization
US-9486519-B2 · Nov 8, 2016 · US
US12357673B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12357673-B2 |
| Application number | US-202117561606-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 23, 2021 |
| Priority date | Jan 10, 2018 |
| Publication date | Jul 15, 2025 |
| Grant date | Jul 15, 2025 |
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 provides a novel fusion protein of Flt3L and albumin and its use to increase the Flt3L half-life in vivo and to deliver Flt3L to immune cells in a subject to enhance alternative dendritic cell populations. Use of the fusion protein in combination with other chemotherapeutic, radiotherapeutic and immunotherapeutic methods are also provided.
Opening claim text (preview).
The invention claimed is: 1. A method of treating cancer in a mammalian subject in need thereof, comprising: administering to the mammalian subject an effective amount of a composition comprising a polypeptide comprising albumin protein linked to a FMS-like tyrosine kinase 3 ligand (Flt3L) protein comprising a sequence having at least 80% identity to SEQ ID NO: 1, to thereby treat the cancer in the mammalian subject. 2. The method of claim 1 , wherein the method further comprises administering to the mammalian subject an effective amount of at least one additional chemotherapeutic agent. 3. The method of claim 1 , wherein the method further comprises administering to the mammalian subject an effective amount of an immunotherapeutic agent. 4. The method of claim 3 , wherein the immunotherapeutic agent is a PD-1 inhibitor. 5. The method of claim 1 , wherein the method further comprises administering to the mammalian subject an effective amount of radiation therapy. 6. The method of claim 5 , wherein the radiation therapy is focused radiation therapy. 7. The method of claim 6 , wherein the amount of radiation given is between about 1 gy to about 30 gy. 8. The method of claim 5 wherein the mammalian subject is suffering from human papilloma virus associated cancer. 9. The method of claim 5 wherein the mammalian subject is suffering from colon adenocarcinoma. 10. The method of claim 1 , wherein the albumin protein is human. 11. The method of claim 1 , wherein the Flt3L protein is human. 12. The method of claim 1 wherein the polypeptide comprises a sequence having at least 90% identity to the amino acid sequence of SEQ ID NO: 1. 13. The method of claim 1 wherein the polypeptide comprises a sequence having at least 98% identity to the amino acid sequence of SEQ ID NO: 1. 14. The method of claim 1 wherein the polypeptide comprises the amino acid sequence of SEQ ID NO: 1. 15. The method of claim 1 wherein the mammalian subject is suffering from human papilloma virus associated cancer. 16. The method of claim 1 wherein the mammalian subject is suffering from colon adenocarcinoma. 17. A method of treating cancer in a mammalian subject in need thereof, comprising: administering to the mammalian subject an effective amount of a composition comprising a polypeptide comprising albumin protein linked to a FMS-like tyrosine kinase 3 ligand (Flt3L) protein, to thereby treat the cancer in the mammalian subject, and wherein the albumin protein is murine. 18. The method of claim 17 wherein the Flt3L protein is murine. 19. The method of claim 17 wherein the polypeptide comprises the amino acid sequence of SEQ ID NO: 2. 20. The method of claim 17 wherein the polypeptide comprises the amino acid sequence of SEQ ID NO: 3.
Hybrid peptides {, i.e. peptides covalently bound to nucleic acids, or non-covalently bound protein-protein complexes} · CPC title
Growth factors; Growth regulators · CPC title
Cytokines; Lymphokines; Interferons · CPC title
Albumins · CPC title
Growth factors; Growth regulators · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.