IP Library › Granted Patent US 9,011,848
Granted Patent B2
US 9,011,848 · App. 13/458,964 · Granted Apr 21, 2015

Human binding molecules capable of neutralizing influenza virus H5N1 and uses thereof

Inventors: Edward Norbert Van Den Brink (Halfweg, NL); Cornelis Adriaan De Kruif (De Bilt, NL); Mark Throsby (Utrecht, NL)
Assignee: Crucell Holland B.V.
C07K16/1018A61K47/4853C07K2317/33C12N2760/16111C12N2760/16061C07K2317/76C12N2760/16011C12N2760/00011C12N2760/00061A61K2039/505C07K2317/21C07K2317/34C07K2317/565C07K2317/622C07K2317/92
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Quick Facts
Patent No.
US 9,011,848
App. No.
13/458,964
Granted
Apr 21, 2015
Kind
B2
Abstract

Described are binding molecules such as human monoclonal antibodies that bind to influenza virus H5N1 and have neutralizing activity against influenza virus H5N1. Also described are nucleic acid molecules encoding the antibodies, and compositions comprising the antibodies and methods of identifying or producing the antibodies. The antibodies can be used in the diagnosis, prophylaxis, and/or treatment of an influenza virus H5N1 infection. In certain embodiments, the antibodies provide cross-subtype protection in vivo, such that infections with H5, H2, H6, H9, and H1-based influenza subtypes can be prevented and/or treated.

Claims (21)

1. An isolated binding molecule able to recognize and bind an influenza hemagglutinin protein (HA) and having neutralizing activity against an influenza virus comprising HA of the H5 subtype, wherein the binding molecule is selected from the group consisting of:

a) a binding molecule comprising a heavy chain CDR1 region of SEQ ID NO:1, a heavy chain CDR2 region of SEQ ID NO:2, a heavy chain CDR3 region of SEQ ID NO:3, a light chain CDR1 region of SEQ ID NO:4, a light chain CDR2 region of SEQ ID NO:5, and a light chain CDR3 region of SEQ ID NO:6,

b) a binding molecule comprising a heavy chain CDR1 region of SEQ ID NO:1, a heavy chain CDR2 region of SEQ ID NO:2, a heavy chain CDR3 region of SEQ ID NO:3, a light chain CDR1 region of SEQ ID NO:7, a light chain CDR2 region of SEQ ID NO:8, and a light chain CDR3 region of SEQ ID NO:9,

c) a binding molecule comprising a heavy chain CDR1 region of SEQ ID NO:1, a heavy chain CDR2 region of SEQ ID NO:2, a heavy chain CDR3 region of SEQ ID NO:3, a light chain CDR1 region of SEQ ID NO:10, a light chain CDR2 region of SEQ ID NO:11, and a light chain CDR3 region of SEQ ID NO:12,

d) a binding molecule comprising a heavy chain CDR1 region of SEQ ID NO:1, a heavy chain CDR2 region of SEQ ID NO:2, a heavy chain CDR3 region of SEQ ID NO:3, a light chain CDR1 region of SEQ ID NO:13, a light chain CDR2 region of SEQ ID NO:14, and a light chain CDR3 region of SEQ ID NO:15,

e) a binding molecule comprising a heavy chain CDR1 region of SEQ ID NO:1, a heavy chain CDR2 region of SEQ ID NO:2, a heavy chain CDR3 region of SEQ ID NO:3, a light chain CDR1 region of SEQ ID NO:33, a light chain CDR2 region of SEQ ID NO:34, and a light chain CDR3 region of SEQ ID NO:35, and

f) a binding molecule comprising a heavy chain CDR1 region of SEQ ID NO:1, a heavy chain CDR2 region of SEQ ID NO:2, a heavy chain CDR3 region of SEQ ID NO:3, a light chain CDR1 region of SEQ ID NO:36, a light chain CDR2 region of SEQ ID NO:37, and a light chain CDR3 region of SEQ ID NO:38.

2. The binding molecule of claim 1 , wherein the binding molecule also has neutralizing activity against an influenza virus comprising HA of the H1subtype.

3. The binding molecule of claim 1 , wherein the binding molecule is a human monoclonal antibody.

4. A process for producing the binding molecule of claim 1 , the process comprising:

expressing a recombinant nucleic acid molecule encoding the binding molecule in an appropriate cell so as to produce the binding molecule therefrom.

5. A pharmaceutical composition comprising:

the binding molecule of claim 1 , and

a pharmaceutically acceptable excipient.

6. A method of treating influenza infection in a subject, the method comprising: administering the binding molecule of claim 1 to the subject.

7. The method according to claim 6 , wherein the influenza infection is caused by an influenza virus associated with a pandemic outbreak, or has the potential to be associated with a pandemic outbreak.

8. The method according to claim 7 , wherein the influenza virus strain is selected from the group consisting of H1N1, H5N1, H5N2, H5N8, H5N9, an H2-based strain, and H9N2.

9. The binding molecule of claim 1 wherein the influenza virus is selected from the group consisting of H5N1, H5N2, H5N8, and H5N9.

10. The binding molecule of claim 1 , wherein the binding molecule also has neutralizing activity against an influenza virus comprising HA of the H2, H6and/or H9 subtype.

11. A process for producing the binding molecule of claim 3 , the process comprising:

expressing a recombinant nucleic acid molecule encoding the binding molecule in an appropriate cell so as to produce the binding molecule therefrom.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 7, 2012
From: VAN DEN BRINK, EDWARD N.; DE KRUIF, CORNELIS A.; THROSBY, MARK
To: CRUCELL HOLLAND B. V.
Reel/Frame 028207/0119 →
Priority Claims (4)
EP 06120316 · Sep 7, 2006 · regional
EP 06120644 · Sep 14, 2006 · regional
EP 06125107 · Nov 30, 2006 · regional
EP 07111235 · Jun 28, 2007 · regional
Continuity (3)
Continuation 12310812
Provisional Application 60842930 · Sep 7, 2006
Related Publication 20120276115A1 · Nov 1, 2012