IP Library Granted Patent US 11,612,652
Granted Patent B2
US 11,612,652 · App. 15/775,680 · Granted Mar 28, 2023

Lipids as synthetic vectors to enhance antigen processing and presentation ex-vivo in dendritic cell therapy

Inventors: Frank Bedu-Addo (Carmel, IN); Greg Conn (Madrid, ES); Siva K. Gandhapudi (Blue Ash, OH); Martin Ward (Lexington, KY); Jerold Woodward (Lexington, KY)
Assignee: PDS Biotechnology Corporation
A61K39/39A61K35/14A61K39/00117A61K39/12A61P31/00A61P35/00C12N5/0639A61K2039/5154A61K2039/55505A61K2039/55522A61K2039/55555A61K2039/55572A61K2039/57A61K2039/572A61K2039/585C12N2710/20034
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Quick Facts
Patent No.
US 11,612,652
App. No.
15/775,680
Granted
Mar 28, 2023
Kind
B2
Abstract

The invention covers the use of certain classes of lipids including cationic lipids in ex-vivo dendritic cell therapies. The cationic lipids enhance antigen uptake, processing and presentation of the processed antigens by dendritic cells to CD8+ and CD4+ T-cells via the MHC classes I and II presentation pathways respectively. Antigen uptake via cationic lipid by dendritic cells result in significant lowering of the population of the immune suppressive regulatory T cells in the tumors and a significant increase of the tumor targeting cytotoxic T-cells. Loss of regulatory T cells and increase of tumor specific cytotoxic cells are conducive to effective elimination of the tumors.

Claims (12)

1. A method of altering a tumor microenvironment by reducing the population of regulatory T-cells in the tumor microenvironment comprising:

administering to a subject having a tumor a dendritic cell vaccine composition,

wherein the dendritic cell vaccine composition comprises:

a cationic lipid comprising R-DOTAP; and

a population of isolated dendritic cells, wherein the dendritic cells have been stimulated ex vivo by at least one antigen,

wherein the at least one antigen is a tumor associated antigen specific for the tumor, and

wherein administering the dendritic cell vaccine composition results in the altering of the tumor microenvironment.

2. The method of claim 1 , wherein the tumor-associated antigen may be protein, peptide, RNA or DNA based.

3. The method of claim 1 , wherein the composition further comprises an adjuvant, growth factor, cytokines or an agent that combats immune suppression.

4. The method of claim 1 , wherein the tumor-associated antigen is an HPV antigen.

5. The method of claim 4 , wherein the HPV antigen is HVP16E7.

6. The method of claim 3 , wherein the cytokine is GM-CSF.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 9, 2018
From: BEDU-ADDO, FRANK; CONN, GREG; GANDHAPUDI, SIVA K.; WARD, MARTIN; WOODWARD, JEROLD
To: PDS BIOTECHNOLOGY CORPORATION
Reel/Frame 047460/0783 →
Continuity (3)
Provisional Application 62404504 · Oct 5, 2016
Provisional Application 62254794 · Nov 13, 2015
Related Publication 20180353599A1 · Dec 13, 2018
Cited By (2)
US 12,201,685 US 12,551,460