IP Library Granted Patent US 12,280,123
Granted Patent B2
US 12,280,123 · App. 17/575,488 · Granted Apr 22, 2025

Recombinant adenoviruses carrying transgenes

Inventors: Christopher Larson (San Diego, CA); Bryan Oronsky (Los Altos Hills, CA); Tony R. Reid (San Diego, CA)
Assignee: EPICENTRX, INC.
A61K47/6829A61K35/761A61K47/6851A61K47/6901A61K48/0025A61K48/0066A61K48/0083A61P35/00C12N7/025C12N7/045C12N15/62C12N15/85C12N15/86C12N2710/10343
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Quick Facts
Patent No.
US 12,280,123
App. No.
17/575,488
Granted
Apr 22, 2025
Kind
B2
Abstract

Disclosed herein are recombinant adenoviruses with one or more nucleotide sequences inserted between two viral transcription units, formulations comprising the recombinant adenoviruses, and methods of treatment using the recombinant adenoviruses. In some embodiments, the one or more nucleotide sequences are inserted in an IX-E2 insertion site and/or an L5-E4 insertion site.

Claims (42)

1. A recombinant adenovirus comprising a nucleotide sequence inserted in an IX-E2 insertion site, wherein the IX-E2 insertion site is located between the stop codon of adenovirus IX gene and the stop codon of adenovirus IVa2 gene, wherein the nucleotide sequence comprises a promoter, a transgene, and a second polyadenylation signal and the recombinant adenovirus comprises in a 5′ to 3′ orientation:

(i) a first polyadenylation signal;

(ii) a fourth polyadenylation signal;

(iii) the promoter;

(iv) the transgene;

(v) the second polyadenylation signal; and

(vi) a third polyadenylation signal;

wherein the transgene is operably linked to the promoter,

wherein the second polyadenylation signal is the polyadenylation signal of the transgene, and

wherein the fourth polyadenylation signal is in the opposite transcriptional direction of the first polyadenylation signal.

2. The recombinant adenovirus of claim 1 , wherein the nucleotide sequence is inserted between nucleotides corresponding to 4029 and 4093 of the Ad5 genome (SEQ ID NO: 1) or between nucleotides corresponding to 3899 and 3970 of the Ad35 genome (SEQ ID NO: 41).

3. The recombinant adenovirus of claim 1 , wherein the first polyadenylation signal comprises the polyadenylation signal of the IX gene and the third polyadenylation signal is the polyadenylation signal of the adenovirus IVa2 gene.

4. The recombinant adenovirus of claim 1 , wherein the recombinant adenovirus further comprises a nucleotide sequence inserted in an E1b-19K insertion site, an E3 insertion site, or an E4 insertion site.

5. The recombinant adenovirus of claim 1 , wherein the recombinant adenovirus further comprises a nucleotide sequence inserted in an L5-E4 insertion site, wherein the L5-E4 insertion site is located between the stop codon of adenovirus fiber gene and the stop codon of ORF6 or ORF6/7 of adenovirus E4 gene.

6. The recombinant adenovirus of claim 1 , wherein the recombinant adenovirus is capable of selectively replicating in a hyperproliferative cell.

7. The recombinant adenovirus of claim 3 , wherein the recombinant adenovirus is capable of selectively expressing the transgene in a hyperproliferative cell.

8. A recombinant adenovirus comprising a first nucleotide sequence inserted in an IX-E2 insertion site and a second nucleotide sequence inserted in an L5-E4 insertion site, wherein the IX-E2 insertion site is located between the stop codon of adenovirus IX gene and the stop codon of adenovirus IVa2 gene, and wherein the L5-E4 insertion site is located between the stop codon of adenovirus fiber gene and the stop codon of ORF6 or ORF6/7 of adenovirus E4 gene, wherein the first nucleotide sequence comprises a first promoter, a first transgene, and a third polyadenylation signal and the recombinant adenovirus comprises in a 5′ to 3′ orientation:

(i) a first polyadenylation signal;

(ii) a fourth polyadenylation signal;

(iii) the first promoter;

(iv) the first transgene;

(v) the second polyadenylation signal; and

(vi) a third polyadenylation signal;

wherein the first transgene is operably linked to the first promoter,

wherein the second polyadenylation signal is the polyadenylation signal of the first transgene, and

wherein the fourth polyadenylation signal is in the opposite transcriptional direction of the first polyadenylation signal.

9. The recombinant adenovirus of claim 8 , wherein the first nucleotide sequence is inserted between nucleotides corresponding to 4029 and 4093 of the Ad5 genome (SEQ ID NO: 1) or between nucleotides corresponding to 3899 and 3970 of the Ad35 genome (SEQ ID NO: 41).

10. The recombinant adenovirus of claim 8 , wherein the second nucleotide sequence is inserted between nucleotides corresponding to 32785 to 32916 of the Ad5 genome (SEQ ID NO: 1) or between nucleotides corresponding to 31799 and 31821 of the Ad35 genome (SEQ ID NO: 41).

11. The recombinant adenovirus of claim 8 , wherein the first polyadenylation signal is the polyadenylation signal of the IX gene and the third polyadenylation signal is the polyadenylation signal of the adenovirus IVa2 gene.

12. The recombinant adenovirus of claim 8 , wherein the second nucleotide sequence comprises a second promoter, a second transgene, and a sixth polyadenylation signal and the recombinant adenovirus comprises, in a 5′ to 3′ orientation:

(i) a fifth polyadenylation signal;

(ii) the second promoter;

(iii) the second transgene;

(iv) the sixth polyadenylation signal; and

(v) a seventh polyadenylation signal;

wherein the second transgene is operably linked to the second promoter, and

wherein the sixth polyadenylation signal is the polyadenylation signal of the second transgene.

13. The recombinant adenovirus of claim 12 , wherein the fifth polyadenylation signal is the polyadenylation signal of the fiber (L5) gene and the seventh polyadenylation signal is the polyadenylation signal of the ORF6 or ORF6/7 of the adenovirus E4 gene.

14. The recombinant adenovirus of claim 12 , further comprising an eighth polyadenylation signal between the fifth polyadenylation signal and the second promoter, wherein the eighth polyadenylation signal is in the opposite transcriptional direction of the fifth polyadenylation signal.

15. The recombinant adenovirus of claim 8 , wherein the recombinant adenovirus further comprises a third nucleotide sequence inserted in an E1b-19K insertion site, an E3 insertion site, or an E4 insertion site.

16. The recombinant adenovirus of claim 8 , wherein the recombinant adenovirus is capable of selectively replicating in a hyperproliferative cell.

17. The recombinant adenovirus of claim 12 , wherein the recombinant adenovirus is capable of selectively expressing the first transgene and the second transgene in a hyperproliferative cell.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 13, 2022
From: LARSON, CHRISTOPHER; ORONSKY, BRYAN; REID, TONY R.
To: EPICENTRX, INC.
Reel/Frame 062076/0491 →
Continuity (3)
Continuation 15991745 · May 29, 2018
Provisional Application 62511822 · May 26, 2017
Related Publication 20220125946A1 · Apr 28, 2022
References Cited (33)
US 11253608B2 · Larson et al. · 2022 [cited by applicant]
US 20030104625A1 · Cheng et al. · 2003 [cited by applicant]
US 20030133912A1 · Davidson · 2003 [cited by examiner]
US 20040091456A1 · Nakai · 2004 [cited by examiner]
US 20050158278A1 · Vogels et al. · 2005 [cited by applicant]
US 20060292682A1 · Hawkins · 2006 [cited by examiner]
US 20160017294A1 · Reid et al. · 2016 [cited by applicant]
US 20160319304A1 · Brown · 2016 [cited by examiner]
US 20200123571A1 · Burny · 2020 [cited by examiner]
CN 1298451A · 2001 [cited by applicant]
CN 102108355A · 2011 [cited by applicant]
JP 2008507279A · 2008 [cited by applicant]
JP 2017501695A · 2017 [cited by applicant]
WO WO1999055831A2 · 1999 [cited by applicant]
WO WO2000003029A2 · 2000 [cited by applicant]
WO WO2000031285A1 · 2000 [cited by applicant]
WO WO2000052186A1 · 2000 [cited by applicant]
WO WO2006012393A2 · 2006 [cited by applicant]
WO WO2010101921A2 · 2010 [cited by applicant]
WO WO2015097220A1 · 2015 [cited by applicant]
WO WO2016174200A1 · 2016 [cited by applicant]
WO WO2018218240A1 · 2018 [cited by applicant]
Genbank Accession AY601635.1 (Human adenovirus type 5 strain NHRC Ad5FS 7151, complete genome, Apr. 12, 2006 [online], [Retrieved on Aug. 14, 2018]. IDS reference). (Year: 2006). [cited by examiner]
Bett Dissertation, 1995, McMaster University, Ontario, Canada. (Year: 1995). [cited by examiner]
Choi et al., (2013). “Oncolytic Adenovirus Expressing IL-23 and p35 Elicits IFN-[gamma]- and TNF-[alpha]-Co-Producing T Cell-Mediated Antitumor Immunity,” PLoS One, 8(7):1-15. [cited by applicant]
Extended European Search Report and Written Opinion mailed Feb. 22, 2021, for European Patent Application No. 18806954.6, 11 pages. [cited by applicant]
GenBank Accession No. AY601635.1, Human adenovirus type 5 strain NHRC Ad5FS 7151, complete genome, Apr. 12, 2006 [online]. [Retrieved on Aug. 14, 2018). Available online at <https://www.ncbi.nlm.nih.gov/nuccore/AY601635… [cited by applicant]
International Search Report and Written Opinion mailed Oct. 16, 2018, for International Application No. PCT/2018/034888, 11 pages. [cited by applicant]
Larson et al., (2015). “Going Viral: A Review Of Replication-Selective Oncolytic Adenoviruses,” Oncotarget, 6(24):19976-89. [cited by applicant]
Leppard et al., (1997). “E4 Gene Function In Adenovirus, Adenovirus Vector And Adeno-Associated Virus Infections,” J. Gen. Virol., 78:2131-8. [cited by applicant]
Mizuguchi et al., (2000). “IRES-Dependent Second Gene Expression Is Significantly Lower Than Cap-Dependent First Gene Expression In A Bicistronic Vector,” Mol. Ther., 1(4):376-82. [cited by applicant]
NCBI Reference Sequence AC_000008.1, “Human Adenovirus 5, Complete Genome,” Aug. 13, 2018, Retrieved on May 8, 2020, Available online at <https://www.ncbi.nlm.nih.gov/nuccore/AC_000008>, 14 pages. [cited by applicant]
Seila et al., (2008). “Divergent Transcription From Active Promoters,” Science, 322(5909):1849-51. [cited by applicant]