IP Library Granted Patent US 9,492,537
Granted Patent B2
US 9,492,537 · App. 14/585,740 · Granted Nov 15, 2016

Methods and compositions involving immunostimulatory oligodeoxynucleotides

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Quick Facts
Patent No.
US 9,492,537
App. No.
14/585,740
Granted
Nov 15, 2016
Kind
B2
Abstract

Described is an immunostimulatory oligodeoxynucleic acid molecule (ODN) having the structure according to formula (I), wherein any NMP is a 2′ deoxynucleoside monophosphate or monothiophosphate, selected from the group consisting of deoxyadenosine-, deoxyguanosine-, deoxyinosine-, deoxycytosine-, deoxyuridine-, deoxythymidine-, 2-methyl-deoxyinosine-, 5-methyl-deoxycytosine-, deoxypseudouridine-, deoxyribosepurine-, 2-amino-deoxyribosepurine-, -6-S-deoxyguanine-, 2-dimethyl-deoxyguanosine- or N-isopentenyl-deoxyadenosine-monophosphate or -monothiophosphate, NUC is a 2′ deoxynucleoside, selected from the group consisting of deoxyadenosine-, deoxyguanosine-, deoxyinosine-, deoxycytosine-, deoxyuridine-, deoxythymidine-, 2-methyl-deoxyinosine-, 5-methyl-deoxycytosine-, deoxypseudouridine-, deoxyribosepurine-, 2-amino-deoxyribosepurine-, 6-S-deoxyguanine-, 2-dimethyl-deoxyguanosine- or N-isopentenyl-deoxyadenosine, any X is O or S, a and b are integers from 0 to 100 with the proviso that a+b is between 4 and 150, B and E are common groups for 5′ or 3′ ends of nucleic acid molecules, as well as a pharmaceutical composition containing such ODNs.

Claims (4)

1. A method of production of a pharmaceutical composition comprising combining at least one antigen and at least one immunostimulatory oligodeoxynucleotide molecule (ODN) consisting of the sequence oligo-dIC 26-mer (SEQ ID NO:30), wherein the pharmaceutical composition is further defined as comprising 10 ng to 1 mg of the ODN.

2. The method of production according to claim 1 , wherein the pharmaceutical composition further comprises at least one of a polycationic polymer, an antimicrobial peptide, a growth hormone, a cytokine, an anti-inflammatory substance, a pharmaceutically acceptable carrier, a buffer substance or a stabilizer.

3. The method of production according to claim 1 , wherein the at least one antigen is derived from viral or bacterial pathogens, from fungi or parasites, and/or wherein the antigens are tumor antigens or autoimmune disease antigens.

4. The method of production according to claim 2 , wherein the polycationic polymer is a synthetic peptide comprising two KLK-motifs separated by a linker of 3 to 7 hydrophobic amino acids.

Assignments (6)
RELEASE OF SECURITY INTEREST Recorded Nov 10, 2025
From: WILMINGTON TRUST, NATIONAL ASSOCIATION, AS ADMINISTRATIVE AGENT
To: VALNEVA AUSTRIA GMBH; VALNEVA SE; VALNEVA USA, INC.
Reel/Frame 073516/0522 →
SECURITY INTEREST Recorded Mar 4, 2020
From: VALNEVA SE; VALNEVA USA, INC.; VALNEVA AUSTRIA GMBH
To: WILMINGTON TRUST, NATIONAL ASSOCIATION
Reel/Frame 052016/0745 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 30, 2014
From: SCHMIDT, WALTER; LINGNAU, KAREN; SCHELLACK, CAROLA; EGYED, ALENA
To: INTERCELL BIOMEDIZINISCHE FORSCHUNGS-UND ENTWICKLUNGS AG
Reel/Frame 034601/0791 →
CHANGE OF NAME Recorded Dec 30, 2014
From: INTERCELL BIOMEDIZINISCHE FORSCHUNGS-UND ENTWICKLUNGS AG
To: INTERCELL AG
Reel/Frame 034601/0819 →
CHANGE OF NAME Recorded Dec 30, 2014
From: INTERCELL AUSTRIA AG
To: VALNEVA AUSTRIA GMBH
Reel/Frame 034601/0936 →
ASSET TRANSFER AGREEMENT Recorded Dec 30, 2014
From: INTERCELL AG
To: INTERCELL AUSTRIA AG
Reel/Frame 034717/0001 →