IP Library › Granted Patent US 11,850,284
Granted Patent B2
US 11,850,284 · App. 17/823,494 · Granted Dec 26, 2023

Compositions and methods for delivery of nucleic acids to cells

Inventors: Elias Quijano (Durham, CT); Peter Glazer (Guilford, CT)
Assignee: Yale University
A61K47/549A61K47/6807A61K47/6851A61K48/005A61P35/00C07K14/4747C07K14/52C07K16/44C12N15/111C12N15/1135C12N15/87A61K48/00A61K48/0025A61K2039/505C07K2317/24C07K2317/31C07K2317/565C07K2317/622C07K2317/77C07K2319/33C12N15/113C12N2310/11C12N2310/14C12N2310/3181C12N2310/3513C12N2320/32
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Quick Facts
Patent No.
US 11,850,284
App. No.
17/823,494
Granted
Dec 26, 2023
Kind
B2
Abstract

Compositions and methods of use thereof for delivering nucleic acid cargo into cells are provided. The compositions typically include (a) a 3E10 monoclonal antibody or an antigen binding, cell-penetrating fragment thereof; a monovalent, divalent, or multivalent single chain variable fragment (scFv); or a diabody; or humanized form or variant thereof, and (b) a nucleic acid cargo including, for example, a nucleic acid encoding a polypeptide, a functional nucleic acid, a nucleic acid encoding a functional nucleic acid, or a combination thereof. Elements (a) and (b) are typically non-covalently linked to form a complex.

Claims (25)

1. A composition comprising a non-covalent complex of (a) an antibody or antigen-binding fragment thereof, and (b) an mRNA,

wherein the antibody or antigen-binding fragment thereof comprises heavy chain variable region (V H ) complementarity determining regions (CDRs) having the amino acid sequences of SEQ ID NO:16, SEQ ID NO:17, and SEQ ID NO:18, and light chain variable region (V L ) CDRs having the amino acid sequences of SEQ ID NO:24, SEQ ID NO:25, and SEQ ID NO:26.

2. The composition according to claim 1 , wherein the antibody or antigen-binding fragment thereof comprises a V H having an amino acid sequence that is at least 95% identical to SEQ ID NO:2 and a V L having an amino acid sequence that is at least 95% identical to SEQ ID NO:7 or 8.

3. The composition according to claim 2 , wherein the V H has the amino acid sequence of SEQ ID NO:2 and the V L has the amino acid sequence of SEQ ID NO:7 or 8.

4. The composition according to claim 1 , wherein the antibody or antigen-binding fragment thereof comprises a V H having an amino acid sequence that is at least 95% identical to SEQ ID NO: 6 and a V L having an amino acid sequence that is at least 95% identical to an amino acid sequence selected from the group consisting of SEQ ID NOs: 11 and 53-55.

5. The composition according to claim 4 , wherein the V H has an amino acid sequence of SEQ ID NO: 6 and the V L has an amino acid sequence selected from the group consisting of SEQ ID NOs: 11 and 53-55.

6. The composition according to claim 1 , wherein the antibody or antigen-binding fragment thereof is a humanized antibody.

7. The composition according to claim 1 , wherein the antibody or antigen-binding fragment thereof is a monovalent single chain variable fragment (scFv), divalent scFv, or multivalent scFv.

8. The composition of claim 1 , wherein the antibody or antigen-binding fragment thereof is a bispecific antibody.

9. The composition of claim 8 , wherein the bispecific antibody comprises:

a first heavy chain or antigen-binding fragment thereof comprising CDRs having the amino acid sequences of SEQ ID NO:16, SEQ ID NO:17, and SEQ ID NO:18, and a first light chain or antigen binding fragment thereof comprising CDRs having the amino acid sequences of SEQ ID NO:24, SEQ ID NO:25, and SEQ ID NO:26; and

a second heavy chain, or antigen-binding fragment thereof, and a second light chain, or antigen binding fragment thereof, that associate to specifically bind a target cell-type, tissue, or organ.

10. The composition according to claim 1 , wherein the mRNA encodes a polypeptide ligand for a receptor of an immune cell.

11. The composition according to claim 10 , wherein the polypeptide ligand is a cytokine.

12. The composition according to claim 10 , wherein the polypeptide ligand stimulates the immune system of the subject.

13. The composition according to claim 1 , wherein the mRNA encodes a polypeptide that is defective in a genetic disease.

14. The composition according to claim 13 , wherein the mRNA encodes dystrophin.

15. The composition according to claim 13 , wherein the mRNA encodes utrophin.

16. The composition according to claim 1 , wherein the mRNA encodes an antigen.

17. The composition according to claim 16 , wherein the antigen is a viral antigen.

18. The composition according to claim 17 , wherein the viral antigen is a SARS-CoV-2 antigen.

19. The composition according to claim 1 , wherein the mRNA encodes a pro-apoptotic factor.

20. The composition according to claim 19 , wherein the pro-apoptotic factor is a BH3-only pro-apoptotic protein.

21. The composition according to claim 1 , wherein the mRNA encodes a tumor suppressor.

22. The composition according to claim 1 , further comprising a pharmaceutically acceptable excipient.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 21, 2023
From: QUIJANO, ELIAS; GLAZER, PETER
To: YALE UNIVERSITY
Reel/Frame 064338/0064 →
Continuity (5)
Continuation 17638642
Continuation In Part PCTUS2019048962 · Aug 30, 2019
Continuation In Part PCTUS2019048953 · Aug 30, 2019
Provisional Application 62944281 · Dec 5, 2019
Related Publication 20230093888A1 · Mar 30, 2023
Cited By (2)
US 12,441,814 US 12,485,180