IP Library Granted Patent US 12,391,745
Granted Patent B2
US 12,391,745 · App. 17/348,356 · Granted Aug 19, 2025

Adeno-associated virus antibodies and fragments thereof

Inventors: Sohrab Khan (Cambridge, MA); Danielle Griffin (Cambridge, MA); Louise Rodino-Klapac (Cambridge, MA)
Assignee: Sarepta Therapeutics, Inc.
C07K16/081C07K16/08G01N33/53G01N33/54306A01K67/027A01K2217/05C07K2317/33C07K2317/56
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,391,745
App. No.
17/348,356
Granted
Aug 19, 2025
Kind
B2
Abstract

The present disclosure relates to an isolated anti-AAV (adeno-associated virus) antibody or an antigen-binding fragment thereof capable of specifically binding an epitope of AAVrh74 capsid protein and uses thereof.

Claims (19)

1. An isolated anti-AAV (adeno-associated virus) antibody or antigen-binding fragment thereof capable of specifically binding an epitope of an AAV capsid protein, wherein the epitope comprises an amino acid sequence QGAGKDNVDYSS (SEQ ID NO: 45); and wherein the antibody or antigen binding fragment thereof comprises:

a. a heavy chain variable region comprising an amino acid sequence that is identical to the amino acid sequence set forth in SEQ ID NO: 1; and a light chain variable region comprising an amino acid sequence that is identical to the amino acid sequence set forth in SEQ ID NO: 2;

b. a heavy chain variable region comprising an amino acid sequence that is identical to the amino acid sequence set forth in SEQ ID NO: 5; and a light chain variable region comprising an amino acid sequence that is identical to the amino acid sequence set forth in SEQ ID NO: 6;

c. a heavy chain variable region comprising an amino acid sequence that is identical to the amino acid sequence set forth in SEQ ID NO: 13; and a light chain variable region comprising an amino acid sequence that is identical to the amino acid sequence set forth in SEQ ID NO: 14;

d. a heavy chain variable region comprising an amino acid sequence that is identical to the amino acid sequence set forth in SEQ ID NO: 9; and a light chain variable region comprising an amino acid sequence that is identical to the amino acid sequence set forth in SEQ ID NO: 10; or

e. a heavy chain variable region comprising an amino acid sequence that is identical to the amino acid sequence set forth in SEQ ID NO: 17; and a light chain variable region comprising an amino acid sequence that is identical to the amino acid sequence set forth in SEQ ID NO: 18.

2. The isolated antibody or antigen binding fragment thereof of claim 1 , wherein the antibody binds to a capsid protein of AAV8 and/or AAV9 with less affinity as compared to a capsid protein of AAVrh74.

3. The isolated antibody or antigen binding fragment thereof of claim 1 , wherein the isolated antibody or antigen binding fragment thereof is labeled with a radioactive, enzymatic, or fluorescent group.

4. The isolated antibody or antigen-binding fragment thereof of claim 1 , wherein the antibody is a full-length antibody or an antibody fragment selected from the group consisting of Fab, Fab′, Fab′-SH, Fd, Fv, dAb, F(ab′)2, scFv, bispecific single chain Fv dimers, diabodies, triabodies, and sxFv genetically fused to the same or a different antibody.

5. The isolated antibody or antigen binding fragment thereof of claim 1 , wherein the antibody is a murine antibody, a chimeric murine/human antibody, a human antibody, an engineered antibody, or a humanized antibody.

6. The isolated antibody of claim 5 , wherein the antibody comprises a heavy chain comprising the amino acid sequence set forth in SEQ ID NO: 21 and a light chain comprising the amino acid sequence set forth in SEQ ID NO: 22.

7. The isolated antibody of claim 5 , wherein the antibody comprises a heavy chain comprising the amino acid sequence set forth in SEQ ID NO: 23 and a light chain comprising the amino acid sequence set forth in SEQ ID NO: 24.

8. The isolated antibody of claim 5 , wherein the antibody comprises a heavy chain comprising the amino acid sequence set forth in SEQ ID NO: 25 and a light chain comprising the amino acid sequence set forth in SEQ ID NO: 26.

9. The isolated antibody of claim 5 , wherein the antibody comprises a heavy chain comprising the amino acid sequence set forth in SEQ ID NO: 27 and a light chain comprising the amino acid sequence set forth in SEQ ID NO: 28.

10. A method of detecting a pre-existing antibody against an AAV capsid in a sample from a subject, comprising subjecting the sample to an assay, wherein the antibody or antigen binding fragment thereof of claim 1 is used as a positive control.

11. The method of claim 10 , wherein the assay is an immunoassay.

12. The method of claim 10 , wherein the assay is an immunofluorescence assay, an immunohistochemical assay, a Western blot, a direct enzyme-linked immunosorbent assay (ELISA), an indirect ELISA, a sandwich ELISA, a competitive ELISA, a reverse ELISA, a chemiluminescence assay, a radioimmunoassay, or an immunoprecipitation assay.

13. The method of claim 10 , wherein the assay is an ElectroChemiLuminiescence Immunoassay (ECLIA).

14. The method of claim 10 , further comprising quantifying the pre-existing antibody through an absorbance reading.

Assignments (2)
SECURITY INTEREST Recorded May 7, 2025
From: SAREPTA THERAPEUTICS, INC.
To: JPMORGAN CHASE BANK, N.A. AS ADMINISTRATIVE AGENT
Reel/Frame 071218/0445 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 30, 2021
From: KHAN, SOHRAB; GRIFFIN, DANIELLE; RODINO-KLAPAC, LOUISE
To: SAREPTA THERAPEUTICS, INC.
Reel/Frame 057330/0927 →
Continuity (2)
Provisional Application 63038957 · Jun 15, 2020
Related Publication 20210388064A1 · Dec 16, 2021
References Cited (38)
US 4816567A · Cabilly et al. · 1989 [cited by applicant]
US 5225539A · Winter · 1993 [cited by applicant]
US 5530101A · Queen et al. · 1996 [cited by applicant]
US 5585089A · Queen et al. · 1996 [cited by applicant]
US 5693762A · Queen et al. · 1997 [cited by applicant]
US 5814318A · Lonberg · 1998 [cited by examiner]
US 6180370B1 · Queen et al. · 2001 [cited by applicant]
US 11472876B2 · Short · 2022 [cited by examiner]
US 20150111955A1 · High · 2015 [cited by examiner]
WO WO2013123503A1 · 2013 [cited by applicant]
WO WO2016176212A1 · 2016 [cited by applicant]
WO WO2021257497A1 · 2021 [cited by applicant]
Tseng et al. (2016) J. Virol. Meth., vol. 236, 105-110. [cited by examiner]
Bolton et al. (Apr. 2020) Malar. J. vol. 19:159, p. 1-13. [cited by examiner]
Vajdos et al. (2002) J. Mol. Biol., vol. 320, 415-428. [cited by examiner]
Chen et al. (1992) J. Exp. Med., vol. 176, 855-866. [cited by examiner]
Sela-Culang et al. (2013) Frontiers in Immunology, vol. 4, pp. 1-13. [cited by examiner]
Wilson et al. (1998) J. Exp. Med., vol. 187(1), 59-70. [cited by examiner]
Bird, R. E., et al., “Single-chain antigen-binding proteins,” [cited by applicant]
Blacklow, N. R., et al., “Serologic evidence for human infection with adenovirus-associated viruses,” [cited by applicant]
Boutin, S., et al., “Prevalence of serum IgG and neutralizing factors against adeno-associated virus (AAV) types 1, 2, 5, 6, 8, and 9 in the healthy population: implications for gene therapy using AAV vectors,” [cited by applicant]
Brennan, M., et al., “Preparation of bispecific antibodies by chemical recombination of monoclonal immunoglobulin G1 fragments,” [cited by applicant]
Carter, P., et al., “High level [cited by applicant]
Chirmule, N., et al., “Immune responses to adenovirus and adeno-associated virus in humans,” [cited by applicant]
Chothia, C., and Lesk, A. M., “Canonical structures for the hypervariable regions of immunoglobulins,” [cited by applicant]
Erles, K., et al., “Update on the prevalence of serum antibodies (IgG and IgM) to adeno-associated virus (AAV),” [cited by applicant]
Harlow, E., and Lane, D., eds., “Chapter 14: Immunoassays,” pp. 553-612, Cold Spring Harbor Laboratory, United States (1988). [cited by applicant]
Huston, J. S., et al., “Protein engineering of antibody binding sites: recovery of specific activity in an anti-digoxin single-chain Fv analogue produced in [cited by applicant]
Kabat, E. A., et al., “Unusual distributions of amino acids in complementarity-determining (hypervariable) segments of heavy and light chains of immunoglobulins and their possible roles in specificity of antibody-combin… [cited by applicant]
Kabat et al., “Sequences of proteins of immunological interest,” U.S. Dept. of Health and Human Services, United States (1991). [cited by applicant]
MacCallum, R. M., et al., “Antibody-antigen interactions: contact analysis and binding site topography,” [cited by applicant]
Mayor, H. D., et al., “Antibodies to adeno-associated satellite virus and herpes simplex in sera from cancer patients and normal adults,” [cited by applicant]
McCafferty, J., et al., “Phage antibodies: filamentous phage displaying antibody variable domains,” [cited by applicant]
Morimoto, K., and Inouye, K., “Single-step purification of F(ab′)2 fragments of mouse monoclonal antibodies (immunoglobulins G1) by hydrophobic interaction high performance liquid chromatography using TSKgel Phenyl-5PW,” [cited by applicant]
Morrison, S. L., “Transfectomas provide novel chimeric antibodies,” [cited by applicant]
Parks, W. P., et al., “Seroepidemiological and ecological studies of the adenovirus-associated satellite viruses,” [cited by applicant]
International Search Report and Written Opinion for International Application No. PCT/US2021/037314, European Patent Office, Netherlands, mailed on Sep. 29, 2021, 10 pages. [cited by applicant]
Co-pending Application, U.S. Appl. No. 17/478,645, inventors Khan, S., et al., filed on Sep. 17, 2021 (Not yet Published). [cited by applicant]