IP Library Granted Patent US 10,561,741
Granted Patent B2
US 10,561,741 · App. 15/553,855 · Granted Feb 18, 2020

Nanoparticle conjugates and uses thereof

Inventors: Paolo Serafini (Miami Shores, FL); Jennifer Vella (Lebanon, NH); Vincenzo Bronte (Abano Terme, IT); Pirouz Daftarian (Palmetto Bay, FL); Angel Kaifer (Coral Gables, FL); Serena Zilio (Miami, FL)
Assignee: UNIVERSITY OF MIAMI
A61K47/6935A61K31/683A61K31/713A61K47/595A61K47/642A61K49/0004A61P35/00C12N15/1135C12N2310/122C12N2310/141C12N2310/3513C12N2310/531
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Quick Facts
Patent No.
US 10,561,741
App. No.
15/553,855
Granted
Feb 18, 2020
Kind
B2
Abstract

Described herein are nanoparticle-based compositions, kits and methods and platforms for delivering one or more nucleic acids to a myeloid cell.

Claims (16)

1. A nanoparticle comprising a charged polymeric dendrimer conjugated to a peptide that specifically binds to IL4Rα expressed on a cell, wherein the peptide that specifically binds to the IL4Rα expressed on myeloid cells is [acetyl]LQRLFRAFR[Abu]LD[Ahx]-C-amide (SEQ ID NO. 1).

2. The nanoparticle of claim 1 , wherein the cell is selected from the group consisting of a myeloid cell, a B cell, a tumor cell and a tumor stromal cell.

3. The nanoparticle of claim 2 , wherein the myeloid cell is a tumor-educated myeloid cell.

4. The nanoparticle of claim 1 , further comprising one or more nucleic acid molecules.

5. The nanoparticle of claim 4 , wherein the one or more nucleic acid molecules is selected from the group consisting of DNA, RNA, shRNA, siRNA, miRNA, an antagomir and RNA sponge.

6. The nanoparticle of claim 5 , wherein the one or more nucleic acid molecule is a shRNA.

7. The nanoparticle of claim 6 , wherein the shRNA is selected from the group consisting of STAT3 shRNA, C-EBPβ shRNA, CCR1 shRNA, CCR2 shRNA and CCR5 shRNA.

8. The nanoparticle of claim 4 , wherein the nucleic acid molecules comprise a combination of STAT3 shRNA and C-EBPβ shRNA, or a combination of CCR1 shRNA, CCR2 shRNA and CCR5 shRNA.

9. The nanoparticle of claim 4 , wherein the nucleic acid molecule comprises miR-142-3p.

10. The nanoparticle of claim 1 , wherein the dendrimer is a PAMAM dendrimer.

11. The nanoparticle of claim 10 , wherein the PAMAM dendrimer is selected from the group consisting of a aG4 dendrimer, G5 dendrimer, a G6 dendrimer and a G7 dendrimer.

12. A method of screening for nucleic acids that modulate the suppressive activity of a myeloid cell comprising

(a) contacting the cell with a nanoparticle comprising

(i) the nanoparticle according to claim 1 ,

(ii) one or more candidate nucleic acids; and

(b) determining whether the suppressive activity of the cell is modulated.

Assignments (2)
CONFIRMATORY LICENSE Recorded Jun 17, 2020
From: UNIVERSITY OF MIAMI SCHOOL OF MEDICINE
To: THE GOVERNMENT OF THE UNITED STATES, AS REPRESENTED BY THE SECRETARY OF THE ARMY
Reel/Frame 052960/0901 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 24, 2019
From: SERAFINI, PAOLO; VELLA, JENNIFER; BRONTE, VINCENZO; DAFTARIAN, PIROUZ; KAIFER, ANGEL; ZILIO, SERENA
To: UNIVERSITY OF MIAMI
Reel/Frame 049848/0778 →
Continuity (2)
Provisional Application 62127566 · Mar 3, 2015
Related Publication 20180243443A1 · Aug 30, 2018