Nucleic acid comprising or coding for a histone stem-loop and a poly(A) sequence or a polyadenylation signal for increasing the expression of an encoded protein

Patent metadata

Field	Value
Publication number	US-9234013-B2
Application number	US-201113321474-A
Country	US
Kind code	B2
Filing date	Aug 12, 2011
Priority date	Aug 13, 2010
Publication date	Jan 12, 2016
Grant date	Jan 12, 2016

Abstract

The present application describes a coding nucleic acid sequence, particularly a messenger RNA (mRNA), comprising or coding for a histone stem-loop and a poly(A) sequence or a polyadenylation signal and the use thereof for increasing the expression of an encoded protein. It also discloses its use for the preparation of a pharmaceutical composition, especially a vaccine e.g. for the use in the treatment of tumors and cancer diseases, cardiovascular diseases, infectious diseases, autoimmune diseases or genetic diseases, or in gene therapy. The present invention further describes an in vitro transcription method, in vitro methods for increasing the expression of a protein using the nucleic acid comprising or coding for a histone stem-loop and a poly(A) sequence or a polyadenylation signal and an ex vivo and in vivo method.

First claim

The invention claimed is:

1. A method of inducing or enhancing an immune response to a polypeptide in a patient comprising providing the patient with a composition comprising an isolated nucleic acid molecule comprising:
a) a coding region encoding the polypeptide, said polypeptide coding region selected from the group consisting of a cancer antigen, a tumor antigen, and an infectious disease antigen, wherein the coding region does not code for histone proteins, reporter proteins selected from enhanced green fluorescent protein (EGFP) and Luciferase and marker or selection proteins selected from alpha-Globin, Galactokinase and Xanthine:guanine phosphoribosyl transferase (GPT),
b) at least one histone stem-loop, and
c) a poly(A) sequence or a polyadenylation signal.

2. The method of claim 1 , wherein the nucleic acid does not contain one of the components of the group consisting of: a sequence encoding a ribozyme, a viral nucleic acid sequence, a histone stem-loop processing signal, a Neo gene, an inactivated promoter sequence, and an inactivated enhancer sequence.

3. The method of claim 1 , wherein the nucleic acid does not contain a ribozyme, and one of the group consisting of: a Neo gene, an inactivated promotor sequence, an inactivated enhancer sequence, and a histone stem-loop processing signal.

4. The method of claim 1 , wherein the nucleic acid is an RNA.

5. The method of claim 1 , wherein the poly(A) sequence comprises a sequence of about 25 to about 400 adenosine nucleotides.

6. The method of claim 1 , wherein the polyadenylation signal comprises the consensus sequence NNUANA, AAUAAA, or AUUAAA.

7. The method of claim 1 , wherein the coding region encodes a tumor antigen, a viral antigen, a protozoal antigen, or a bacterial antigen.

8. The method of claim 1 , wherein the nucleic acid is monocistronic or bicistronic.

9. The method of claim 1 , wherein the composition comprises a pharmaceutically acceptable carrier.

10. The method of claim 1 , wherein the patient has a disease selected from the group consisting of cancer diseases, tumor diseases, and infectious diseases.

11. The method of claim 1 , wherein at least one guanosine, uridine, adenosine, thymidine, or cytidine position of the nucleic acid molecule is substituted with a nucleotide analogue selected from 2-amino-6-chloropurineriboside-5′-triphosphate, 2-aminoadenosine-5′-triphosphate, 2-thiocytidine-5′-triphosphate, 2-thiouridine-5′-triphosphate, 4-thiouridine-5′-triphosphate, 5-aminoallylcytidine-5′-triphosphate, 5-aminoallyluridine-5′-triphosphate, 5-bromocytidine-5′-triphosphate, 5-bromouridine-5′-triphosphate, 5-iodocytidine-5′-triphosphate, 5-iodouridine-5′-triphosphate, 5-methylcytidine-5′-triphosphate, 5-methyluridine-5′-triphosphate, 6-azacytidine-5′-triphosphate, 6-azauridine-5′-triphosphate, 6-chloropurineriboside-5′-triphosphate, 7-deazaadenosine-5′-triphosphate, 7-deazaguanosine-5′-triphosphate, 8-azaadenosine-5′-triphosphate, 8-azidoadenosine-5′-triphosphate, benzimidazole-riboside-5′-triphosphate, N1-methyladenosine-5′-triphosphate, N1-methylguanosine-5′-triphosphate, N6-methyladenosine-5′-triphosphate, O6-methylguanosine-5′-triphosphate, pseudouridine-5′-triphosphate, puromycin-5′-triphosphate, and xanthosine-5′-triphosphate.

12. The method of claim 4 , wherein the RNA comprises a 5′ cap structure and a poly(A) sequence of about 25 to about 400 adenosine nucleotides.

13. The method of claim 1 , wherein the composition is administered intradermally.

14. The method of claim 1 , wherein further comprising administering an adjuvant to the patient.

15. The method of claim 1 , wherein the nucleic acid molecule further comprises a sequence of at least 10 consecutive cytidines.

16. The method of claim 1 , wherein the nucleic acid molecule further comprises a stabilizing sequence.

17. The method of claim 16 , wherein the stabilizing sequence comprises a sequence from the alpha globin 3′ UTR, positioned 3′ relative to the polypeptide coding region of the nucleic acid molecule.

18. The method of claim 1 , wherein the composition further comprises a cationic or polycationic compound in complex with the nucleic acid molecule.

19. The method of claim 18 , wherein the polycationic compound is a polycationic polypeptide.

Assignees

• Thess Andreas
• Schlake Thomas
• Probst Jochen
• Curevac Ag

Inventors

• Thess Andreas
• Schlake Thomas
• Probst Jochen

Classifications

• A61P37/08

  Antiallergic agents (antiasthmatic agents A61P11/06; ophthalmic antiallergics A61P27/14) · CPC title

• A61P9/00

  Drugs for disorders of the cardiovascular system · CPC title

• A61P43/00

  Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title

• A61P37/06

  Immunosuppressants, e.g. drugs for graft rejection · CPC title

• A61P5/00

  Drugs for disorders of the endocrine system · CPC title