IP Library Granted Patent US 11,207,339
Granted Patent B2
US 11,207,339 · App. 15/772,134 · Granted Dec 28, 2021

Targeted cancer therapy

Inventors: Roy Lobb (Westwood, MA); Paul David Rennert (Holliston, MA); John Todd Schiller (Kensington, MD)
Assignees: The United States of America, as Represented by the Secretary, Department of Health and Human Services; Aleta Biotherapeutics Inc.
A61K31/7088A61K9/0019A61K35/761A61K35/763A61K35/765A61K35/766A61K35/768A61K39/0011A61K39/00115A61K39/00116A61K39/00117A61K39/001104A61K39/001106A61K39/001109A61K39/001112A61K39/001113A61K39/001119A61K39/001122A61K39/001124A61K39/001166A61K39/001168A61K39/001171A61K39/001174A61K39/001182A61K39/001186A61K39/001188A61K39/001191A61K39/001192A61K39/001195C07K14/70503A61K2039/5152A61K2039/5156A61K2039/5158Y02A50/30
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Quick Facts
Patent No.
US 11,207,339
App. No.
15/772,134
Granted
Dec 28, 2021
Kind
B2
Abstract

Some embodiments of the present disclosure are directed to methods that include delivering to a subject a nucleic acid encoding an antigen, wherein the nucleic acid is delivered via a tumor-selective vehicle or via intratumoral injection, and delivering to the subject an immune cell expressing a receptor that binds to the antigen.

Claims (19)

1. A method comprising

(i) delivering to a tumor of a subject an engineered nucleic acid encoding an antigen, wherein the engineered nucleic acid is delivered via a tumor-selective vehicle or via intratumoral injection, wherein the tumor expresses the antigen and

(ii) administering to the subject an immune cell expressing a chimeric receptor that binds to the antigen; wherein the antigen comprises an epitope of CD19, CD20, CD21, CD22, CD45, BCMA, HER2 (ErbB2), EGFRvIII, B7-H3, B7-H6, FAP, FRa, EpCAM, GD2, ROR1, PSMA, or IL13Ralpha2, wherein the immune cell binds to the expressed antigen, thereby resulting in killing of the tumor.

2. The method of claim 1 , wherein the tumor antigen is or comprises an epitope of CD19.

3. The method of claim 2 , wherein the tumor antigen is selected from full length CD19, a fragment of CD19, or a linear epitope of CD19.

4. The method of claim 1 , wherein the engineered nucleic acid encoding the antigen is encapsulated within the tumor-selective vehicle.

5. The method of claim 1 , wherein tumor-selective vehicle is a virus or a pseudovirus.

6. The method of claim 5 , wherein the tumor-selective vehicle is an oncolytic virus, a chimeric virus, a virus that is modified to target tumor cells, a papillomavirus, or a pseudovirus.

7. The method of claim 6 , wherein the tumor-selective vehicle is an oncolytic virus selected from an adenovirus, a vaccinia virus, a Sindbis virus, a Seneca valley virus, a Coxsackie virus, a measles virus, a reovirus, a vaccinia virus, a Newcastle disease virus, a vesicular stomatitis virus, a herpes simplex virus, a poliovirus, and a parvovirus.

8. The method of claim 6 , wherein the tumor-selective vehicle is a chimeric virus obtained from engineering adeno-associated viruses and bacteriophages that display tumor selective peptides.

9. The method of claim 6 , wherein the tumor-selective vehicle is an adeno-associated virus (AAV) that is modified to target tumor cells.

10. The method of claim 6 , wherein the tumor-selective vehicle is a human papillomavirus, a modified human papillomavirus, a non-human papillomavirus, or a modified non-human papillomavirus.

11. The method of claim 1 , wherein tumor-selective vehicle is or comprises a natural polymer, a synthetic polymer, a cationic peptide, a cell-penetrating peptide, a biodegradable nanoparticle, a liposome, a lipoplex, a polyplex, a micelle, a dendrimer, a gel, a mucoadhesive or a silicon nanoneedle.

12. The method of claim 1 , wherein the tumor-selective vehicle comprises a tumor-targeting agent.

13. The method of claim 1 , wherein the engineered nucleic acid encoding an antigen is a deoxyribonucleic acid (DNA) or a ribonucleic acid (RNA).

14. The method of claim 13 , wherein the engineered nucleic acid encoding an antigen is a messenger RNA (mRNA).

15. The method of claim 1 , wherein the immune cell is leukocyte.

16. The method of claim 1 , wherein the immune cell is a T cell, a B cell, an NK cell, an NKT cell, or a dendritic cell.

17. The method of claim 1 , wherein the tumor-selective vehicle is delivered via a parenteral, enteric or topical route, or wherein the engineered nucleic acid is injected into the tumor.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 13, 2019
From: LOBB, ROY; RENNERT, PAUL DAVID
To: ALETA BIOTHERAPEUTICS INC.
Reel/Frame 048315/0808 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 12, 2019
From: SCHILLER, JOHN TODD
To: THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES
Reel/Frame 048303/0969 →
Continuity (2)
Provisional Application 62249013 · Oct 30, 2015
Related Publication 20180311269A1 · Nov 1, 2018