IP Library Patent Application 16235559
Patent Application
App. No. 16/235,559

INDUCIBLE EXPRESSION CASSETTE, AND USES THEREOF

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Patent No.
US None
App. No.
16/235,559
Abstract

An expression cassette including a gene of interest under the control of an inducible promoter, characterized in that said inducible promoter includes at least one CARE regulatory sequence (C/EBP-ATF responsive element) and a minimal promoter. Also, a vector and a host cell, as well as to a pharmaceutical composition including such a cassette, and to the use thereof for treating diseases by gene therapy.

Claims (36)

1 . A nucleic acid construct that directs expression in a mammal cell, comprising:

(i) an inducible promoter consisting of a minimal promoter and one or more ATF4-binding CARE (C/EBP-ATF Responsive Element) regulatory sequence, wherein the minimal promoter is the minimal promoter of TK, CMV or HSP gene, wherein ATF4-binding CARE (C/EBP-ATF Responsive Element) regulatory sequence is selected form the group consisting of SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO: 4, SEQ ID NO:5 and SEQ ID NO:6, and

(ii) a heterologous coding sequence, wherein the heterologous coding sequence is operably linked to the inducible promoter.

2 . The nucleic acid construct of claim 1 , wherein the inducible promoter comprises six ATF4-binding CARE (C/EBP-ATF Responsive Element) regulatory sequence selected from the group consisting of SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO: 4, SEQ ID NO:5 and SEQ ID NO:6.

3 . The nucleic acid construct of claim 1 , wherein the minimal promoter is the thymidine kinase minimal promoter of SEQ ID NO: 1.

4 . The nucleic acid construct of claim 1 , wherein the inducible promoter is of SEQ ID NO:7.

5 . The nucleic acid construct of claim 1 , wherein the expression is induced by an essential amino-acid deficiency.

6 . The nucleic acid construct of claim 1 , wherein the heterologous coding sequence is an antisense RNA coding sequence, a ribozyme coding sequence or a polypeptide of interest coding sequence.

7 . The nucleic acid construct of claim 6 , wherein the polypeptide of interest is selected from the group consisting of chemokine, cytokine, cell receptor, receptor ligand, coagulation factor, growth factor, enzyme, enzyme inhibitor, Class-I or Class-II major histocompatibility complex antigen or polypeptides acting on the expression of the corresponding gene, polypeptide capable of inhibiting a viral, bacterial, or parasitic infection or the development thereof, polypeptide acting positively or negatively on apoptosis, cytostatic agents, whole or partial immunoglobulin, toxin, immunotoxin, apolipoprotein, angiogenesis inhibitor, marker, and any other polypeptide having a therapeutic effect on a targeted condition.

8 . The nucleic acid construct of claim 1 , further comprising, upstream of the heterologous coding sequence, a sequence coding for a peptide signal.

9 . An expression vector comprising the nucleic acid construct of claim of claim 1 .

10 . The expression vector of claim 9 , wherein the vector is a plasmid or a viral vector.

11 . The expression vector of claim 10 , wherein the viral vector is a lentiviral vector, an adenoviral vector or a vector derived from an adenovirus-associated virus (AAV).

12 . A recombinant cell comprising the nucleic acid construct of claim 1 or the expression vector of claim 9 .

13 . The recombinant cell of claim 12 , wherein the nucleic acid construct is stably incorporated into its genome.

14 . The recombinant cell of claim 12 , wherein the mammal cell in a human cell.

15 . A pharmaceutical composition comprising the nucleic acid construct of claim 1 .

16 . A kit comprising:

1) a component selected from the group consisting of:

a) one or more nucleic acid of claim 1 , or

b) an expression vector comprising said one or nucleic acid, and

2) Instructions for use of the component in the prevention or treatment of a disease in a human, wherein said disease required using gene therapy.

17 . The kit of claim 16 , further comprising a composition for enforcing an essential amino-acid deficiency.

18 . A method for modulating expression of a heterologous coding sequence in a mammal cell, wherein the expression implies the activation of GCN2 kinase and is mediated by the eIF2a/ATF4 signaling pathway, comprising the steps of:

a) providing a mammalian cell, wherein the cell comprises the nucleic acid construct of claim 1 or an expression vector comprising said nucleic acid construct,

b) contacting the cell with a composition in which one or more essential amino-acid is absent, wherein the deficiency in one or more essential amino acid activates the GCN2 kinase such that the eIF2a/ATF4 signaling pathway is activated.

19 . The method of claim 18 , wherein the mammal cell is a human cell.

20 . The method of claim 19 , wherein the human cell is a primary or tumor cell of hematopoietic, muscular, cardiac, pulmonary, tracheal, hepatic, epithelial, fibroblast or stem cell origin.

21 . The method of claim 18 , wherein the heterologous coding sequence is an antisense RNA coding sequence, a ribozyme coding sequence or a polypeptide of interest coding sequence.

22 . The method of claim 21 , wherein the polypeptide of interest is selected from the group consisting of chemokine, cytokine, cell receptor, receptor ligand, coagulation factor, growth factor, enzyme, enzyme inhibitor, Class-I or Class-II major histocompatibility complex antigen or polypeptides acting on the expression of the corresponding gene, polypeptide capable of inhibiting a viral, bacterial, or parasitic infection or the development thereof, polypeptide acting positively or negatively on apoptosis, cytostatic agents, whole or partial immunoglobulin, toxin, immunotoxin, apolipoprotein, angiogenesis inhibitor, marker, and any other polypeptide having a therapeutic effect on a targeted condition.

23 . A method for modulating expression of a heterologous gene of interest within a mammal, comprising the steps of:

a) obtaining a mammal having at least some cells comprising the nucleic acid construct of claim 1 or an expression vector comprising said nucleic construct of claim 9 ,

b) feeding the mammal with a composition for enforcing an essential amino-acid deficiency.

24 . The method of claim 23 , wherein the mammal is a human.

25 . The method of claim 23 , wherein the mammal suffers from a disease selected in the group consisting of proliferative diseases, infectious, genetic diseases, cardiovascular diseases or neurological diseases.

26 . The method of claim 23 , wherein the composition is applied and removed for a plurality of cycles, wherein a cycle comprises applying and removing the composition.

Assignments (3)
CORRECTIVE ASSIGNMENT TO CORRECT THE RECEIVING PARTY DATA PREVIOUSLY RECORDED ON REEL 052469 FRAME 0167. ASSIGNOR(S) HEREBY CONFIRMS THE CHANGE OF NAME. Recorded Apr 28, 2020
From: INSTITUT NATIONAL DE LA RECHERCHE AGRONOMIQUE (INRA)
To: INSTITUT NATIONAL DE RECHERCHE POUR L'AGRICULTURE, L'ALIMENTATION ET L'ENVIRONNEMENT
Reel/Frame 052510/0160 →
CHANGE OF NAME Recorded Apr 22, 2020
From: INSTITUT NATIONAL DE LA RECHERCHE AGRONOMIQUE (INRA)
To: INSTITUT NATIONAL DE RECHERCHE POUR L'AGRICULTURE, L'ALIMENTATION ET L'ENVIRONNEMENT (INRAE)
Reel/Frame 052469/0167 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 15, 2019
From: FAFOURNOUX, PIERRE; BRUHAT, ALAIN; JOUSSE, CELINE; MAURIN, ANNE-CATHERINE; AVEROUS, JULIEN
To: INSTITUT NATIONAL DE LA RECHERCHE AGRONOMIQUE (INRA); CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS)
Reel/Frame 048007/0376 →