IP Library Granted Patent US 9,376,485
Granted Patent B2
US 9,376,485 · App. 14/380,978 · Granted Jun 28, 2016

Neutralizing antibody for epstein barr virus-associated disease

Inventors: Frederick C. S. Wang (Chestnut Hill, MA); Mark H. Fogg (Newton, MA)
Assignee: The Brigham and Women's Hospital, Inc.
C07K16/085A61K39/42A61K2039/505C07K2316/96C07K2317/24C07K2317/56C07K2317/76
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Quick Facts
Patent No.
US 9,376,485
App. No.
14/380,978
Granted
Jun 28, 2016
Kind
B2
Abstract

Described herein are compositions, methods, and uses relating to an EBV-neutralizing antibody.

Claims (75)

1. A composition comprising a purified, recombinant, humanized EBV-neutralizing antibody, wherein the antibody comprises the following CDRs:

CDR H1,

GSSFTDYT;

(SEQ ID NO: 5)

CDR H2,

INPYNGGT;

(SEQ ID NO: 6)

CDR H3,

AGGLRRVNWFAY;

(SEQ ID NO: 7)

CDR L1,

TGAVTTSNY;

(SEQ ID NO: 14)

CDR L2,

GTN;

(SEQ ID NO: 15)

and

CDR L3,

VLWHSNHWV.

(SEQ ID NO: 16)

2. The composition of claim 1 , wherein the antibody has a heavy chain variable region having the amino acids:

(SEQ ID NO: 1)

EVQLQQSGPELVKPGTSMKISCKASGSSFTDYTMNWMKQSHGKNLEWIGL

INPYNGGTRYNQKFKGKATLTLDKSSSTAYMEVLSLTSEDSAVYYCAGGL

RRVNWFAYWGQGTLVSVSA

and

and a variable light chain region having the amino acids:

(SEQ ID NO: 4)

QAVLTQESALTTSPGETVTLTCRSSTGAVTTSNYANWVQEKPDHLFTGLI

GGTNNRVPGVPARFSGSLIGDKAALTITGAQTEDEAIYFCVLWHSNHWVF

GGGTKLTVL;

and said variable heavy and light chain regions are linked to human constant regions.

3. The composition of claim 1 , wherein the purified, recombinant, humanized EBV-neutralizing antibody comprises human variable chain framework regions and the following CDRs:

CDR H1,

GSSFTDYT;

(SEQ ID NO: 5)

CDR H2,

INPYNGGT;

(SEQ ID NO: 6)

CDR H3,

AGGLRRVNWFAY;

(SEQ ID NO: 7)

CDR L1,

TGAVTTSNY;

(SEQ ID NO: 14)

CDR L2,

GTN;

(SEQ ID NO: 15)

and

CDR L3,

VLWHSNHWV.

(SEQ ID NO: 16)

4. A method for treating infectious mononucleosis in a subject suffering from genetic immunodeficiency comprising administering to the subject a pharmaceutical composition comprising a purified, recombinant, humanized EBV-neutralizing antibody of claim 1 .

5. The method of claim 4 , wherein the purified, recombinant, humanized EBV-neutralizing antibody comprises the following CDRs:

CDR H1,

GSSFTDYT;

(SEQ ID NO: 5)

CDR H2,

INPYNGGT;

(SEQ ID NO: 6)

CDR H3,

AGGLRRVNWFAY;

(SEQ ID NO: 7)

CDR L1,

TGAVTTSNY;

(SEQ ID NO: 14)

CDR L2,

GTN;

(SEQ ID NO: 15)

and

CDR L3,

VLWHSNHWV;

(SEQ ID NO: 16)

wherein the CDRs are linked to human variable chain framework regions or human constant chain regions, or both of these.

6. A method of treating EBV-induced lymphoproliferative disease in immunosuppressed subjects, the method comprising administering to the subject a pharmaceutical composition comprising a purified, recombinant, humanized EBV-neutralizing antibody of claim 1 .

Assignments (2)
CONFIRMATORY LICENSE Recorded Aug 31, 2015
From: BRIGHAM AND WOMEN'S HOSPITAL
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 036509/0155 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 2, 2014
From: WANG, FREDERICK C.S.; FOGG, MARK H.
To: THE BRIGHAM AND WOMEN'S HOSPITAL, INC.
Reel/Frame 033650/0812 →
Continuity (2)
Provisional Application 61604574 · Feb 29, 2012
Related Publication 20150064174A1 · Mar 5, 2015