IP Library Granted Patent US 7,741,099
Granted Patent B2
US 7,741,099 · App. 11/665,276 · Granted Jun 22, 2010

Adenoviral vectors and uses thereof

Assignees: Beth Israel Deaconess Medical Center Inc.; Crucell Holland B.V.
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Quick Facts
Patent No.
US 7,741,099
App. No.
11/665,276
Granted
Jun 22, 2010
Kind
B2
Abstract

The present invention relates to recombinant adenoviral vectors based on adenoviruses that encounter pre-existing immunity in a minority of the human population and which harbor a chimeric capsid. The chimeric capsid comprises fiber proteins that have at least the knob domain of a human adenovirus that binds to the Coxsackievirus and Adenovirus Receptor (CAR) and a hexon protein from an adenovirus serotype that encounters pre-existing immunity in a low percentage of the human population.

Claims (27)

1. A batch of recombinant replication-defective adenovirus based upon adenovirus serotype 5 (Ad5), the recombinant replication-defective adenovirus comprising a chimeric hexon protein, wherein in the chimeric hexon protein hypervariable region sequences HVR1 to HVR7 of Ad5 have been replaced with those of Ad48 or of Pan9, in the following manner:

the HVR1 sequence of Ad5 (SEQ ID NO: 17) has been replaced by a sequence selected from the group consisting of SEQ ID NO: 24, and 52,

the HVR2 sequence of Ad5 (SEQ ID NO: 18) has been replaced by a sequence selected from the group consisting of SEQ ID NO: 25, and 53,

the HVR3 sequence of Ad5 (SEQ ID NO: 19) has been replaced by a sequence selected from the group consisting of SEQ ID NO: 26, and 54,

the HVR4 sequence of Ad5 (SEQ ID NO: 20) has been replaced by a sequence selected from the group consisting of SEQ ID NO: 27, and 55,

the HVR5 sequence of Ad5 (SEQ ID NO: 21) has been replaced by a sequence selected from the group consisting of SEQ ID NO: 28, and 56,

the HVR6 sequence of Ad5 (SEQ ID NO: 22) has been replaced by a sequence selected from the group consisting of SEQ ID NO: 29, and 57, and

the HVR7 sequence of Ad5 (SEQ ID NO: 23) has been replaced by a sequence selected from the group consisting of SEQ ID NO: 30, and 58, and

wherein the sequences between the HVR sequences are from Ad5.

2. A recombinant adenovirus comprising a chimeric hexon protein, wherein the sequence of the chimeric hexon protein consists of SEQ ID NO: 12.

3. A batch of recombinant replication defective adenovirus based upon adenovirus serotype 5 (Ad5), the recombinant replication-defective adenovirus, comprising a chimeric hexon protein, wherein the chimeric hexon protein hypervariable region sequences HVR1 to HVR7 of Ad5 have been replaced with those of Ad48 in the following manner:

the HVR1 sequence of Ad5 (SEQ ID NO: 17) has been replaced by an amino acid sequence consisting of SEQ ID NO: 24,

the HVR2 sequence of Ad5 (SEQ ID NO: 18) has been replaced by an amino acid sequence consisting of SEQ ID NO: 25,

the HVR3 sequence of Ad5 (SEQ ID NO: 19) has been replaced by an amino acid sequence consisting of SEQ ID NO: 26,

the HVR4 sequence of Ad5 (SEQ ID NO: 20) has been replaced by an amino acid sequence consisting of SEQ ID NO: 27,

the HVR5 sequence of Ad5 (SEQ ID NO: 21.) has been replaced by an amino acid sequence consisting of SEQ ID NO; 28,

the HVR7 sequence of Ad5 (SEQ ID NO: 22) has been replaced by an amino acid sequence consisting of SEQ ID NO: 29, and

the HVR7 sequence of Ad5 (SEQ ID NO: 23) has been replaced by an amino acid sequence consisting of SEQ ID NO: 30, and wherein the sequences between the HVR sequences are from Ad5.

4. The batch of claim 1 , wherein the replication-defective adenovirus comprises a heterologous nucleic acid of interest.

5. The batch of claim 3 , wherein the replication-defective adenovirus comprises a heterologous nucleic acid of interest.

6. The recombinant adenovirus of claim 2 , wherein the recombinant adenovirus comprises a heterologous nucleic acid of interest.

7. The recombinant adenovirus of claim 2 , comprising an adenoviral genome having a deletion in the E1 region.

8. The recombinant adenovirus of claim 7 , wherein the adenoviral genome further has a deletion in the E3 region.

9. The batch of claim 1 , wherein the replication-defective adenovirus comprises an adenoviral genome having a deletion in the E1 region.

10. The batch of claim 7 , wherein the adenoviral genome further has a deletion in the E3 region.

11. The batch of claim 3 , wherein the replication-defective adenovirus comprises an adenoviral genome having a deletion in the E1 region.

12. The batch of claim 11 , wherein the adenoviral genome further has a deletion in the E3 region.

Assignments (4)
CONFIRMATORY LICENSE Recorded Jul 13, 2016
From: BETH ISRAEL DEACONESS MEDICAL CENTER
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 039328/0038 →
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE SHOULD BE: BETH ISRAEL DEACONESS MEDICAL CENTER INC. PREVIOUSLY RECORDED ON REEL 019202 FRAME 0893. ASSIGNOR(S) HEREBY CONFIRMS THE BETH ISRAEL DEACONESS MEDICAL CENTER INC.. Recorded May 22, 2007
From: BAROUCH, DAN H.
To: BETH ISRAEL DEACONESS MEDICAL CENTER INC
Reel/Frame 019329/0821 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 11, 2007
From: BAROUCH, DAN H.
To: BETH ISREAL DEACONESS MEDICAL CENTER INC.
Reel/Frame 019202/0893 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 11, 2007
From: HAVENGA, MENZO J. E.
To: CRUCELL HOLLAND B.V.
Reel/Frame 019202/0929 →
Priority Claims (1)
EP 04105005 · Oct 13, 2004 · regional
Continuity (3)
Provisional Application 6069772400 · Jul 8, 2005
Provisional Application 6061846900 · Oct 13, 2004
Related Publication 20080199939A1 · Aug 21, 2008