IP Library Granted Patent US 9,533,030
Granted Patent B2
US 9,533,030 · App. 14/418,139 · Granted Jan 3, 2017

Vaccine capable of inducing formation of antibodies directed to proprotein convertase subtilisin/kexin type 9 (PCSK9) in vivo

Inventors: Sylvia Brunner (Vienna, AT); Gergana Galabova (Vienna, AT); Gabriele Winsauer (Vienna, AT); Erika Bilcikova (Bratislava, SK); Claudia Juno (Vienna, AT); Pola Linzmayer-Hirt (Wiener Neudorf, AT); Birgit Schuh (Vienna, AT); Guenther Staffler (Vienna, AT)
Assignee: AFFIRIS AG
A61K39/0005A61K39/385A61K39/39A61K47/4833A61K47/48261A61K47/48284C12N9/6424C12N9/6454C12Y304/21061A61K2039/55505A61K2039/6081
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Quick Facts
Patent No.
US 9,533,030
App. No.
14/418,139
Granted
Jan 3, 2017
Kind
B2
Abstract

The present invention relates to a vaccine capable to induce the formation of antibodies directed to PCSK9 in vivo.

Claims (32)

1. A vaccine, comprising a peptide consisting of 10 to 13 amino acid residues and comprising an amino acid sequence selected from the group consisting of SIPWSLERIT (SEQ ID No. 21), VIPWNLERIL (SEQ ID No. 55), and SVPWNLERIQ (SEQ ID No. 60),

wherein the peptide is coupled or fused to a pharmaceutically acceptable carrier.

2. The vaccine according to claim 1 , wherein the peptide is selected from the group consisting of SIPWSLERIT (SEQ ID NO:21), SIPWSLERITPPR (SEQ ID NO:87), VIPWNLERIL (SEQ ID NO:55), VIPWNLERILPPR (SEQ ID NO:99), SVPWNLERIQ (SEQ ID NO:60), and SVPWNLERIQPPR (SEQ ID NO:106).

3. The vaccine according to claim 1 , wherein the peptide comprises at its N- and/or C-terminus, a cysteine residue bound directly or via a spacer sequence thereto.

4. The vaccine according to claim 1 , wherein the pharmaceutically acceptable carrier is a protein carrier.

5. The vaccine according to claim 4 , wherein the protein carrier is selected from the group consisting of keyhole limpet haemocyanin (KLH), tetanus toxoid (TT), and protein D or diphtheria toxin (DT).

6. The vaccine according to claim 1 , wherein the compound is formulated with an adjuvant.

7. A method comprising treating a disorder caused by hyperlipidemia, hypercholesterolemia and/or atherosclerosis, by administering the vaccine according to claim 1 to an individual in need thereof.

8. A peptide consisting of an amino acid sequence

(SEQ ID No. 1)

X 1 X 2 X 3 WX 4 X 5 X 6 RX 7 (X 8 ) m (X 9 ) n ,

wherein

X 1 is serine or valine,

X 2 is isoleucine or valine,

X 3 is proline,

X 4 is asparagine or serine,

X 5 is leucine,

X 6 is glutamic acid,

X 7 is isoleucine,

X 8 is threonine, leucine, or glutamine,

X 9 is X 10 X 11 X 12 or a C-terminal truncated fragment thereof consisting of 1 or 2 amino acid residues,

X 10 is proline, alanine, or serine,

X 11 is proline, alanine, valine, threonine, or asparagine,

X 12 is arginine, alanine, lysine, serine, or leucine,

provided that

if X 1 is serine, then X 2 , X 4 , and X 8 are either isoleucine, serine, and threonine, or valine, asparagine, and glutamine, and

if X 1 is valine, then X 2 , X 4 , and X 8 are isoleucine, serine, and leucine,

in is 0 or 1,

n is 0 or 1.

9. The peptide according to claim 8 , wherein X 9 is proline-proline-arginine.

10. The peptide according to claim 8 , selected from the group consisting of SIPWSLERIT (SEQ ID No. 21), SIPWSLERITPPR (SEQ ID No. 87), VIPWNLERIL (SEQ ID No. 55), VIPWNLERILPPR (SEQ ID No. 99), SVPWNLERIQ (SEQ ID No. 60), and SVPWNLERIQPPR (SEQ ID No. 106).

11. The peptide according to claim 8 , selected from the group consisting of SIPWSLERIT (SEQ ID No. 21), VIPWNLERIL (SEQ ID No. 55), and SVPWNLERIQ (SEQ ID No. 60).

Assignments (2)
CONFIRMATORY ASSIGNMENT Recorded May 11, 2022
From: AFFIRIS AG
To: AFFIRIS CVD GMBH
Reel/Frame 059929/0690 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 29, 2015
From: BRUNNER, SYLVIA; GALABOVA, GERGANA; WINSAUER, GABRIELE; BILCIKOVA, ERIKA; JUNO, CLAUDIA; LINZMAYER-HIRT, POLA; SCHUH, BIRGIT; STAFFLER, GUENTHER
To: AFFIRIS AG
Reel/Frame 034841/0343 →
Priority Claims (1)
EP 12182241 · Aug 29, 2012 · regional
Continuity (1)
Related Publication 20150306191A1 · Oct 29, 2015