IP Library Granted Patent US 12,692,316
Granted Patent B2
US 12,692,316 · App. 17/784,835 · Granted Jul 28, 2026

Antibodies to canine interleukin-4 receptor alpha

Inventors: Mohamad Morsey (Omaha, NE); Yuanzheng Zhang (Somerset, NJ)
Assignee: INTERVET INC.
C07K16/2866A61P17/00C12N5/0602C12N15/85A61K39/3955C07K2317/24C07K2317/34C07K2317/565C07K2317/76
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Quick Facts
Patent No.
US 12,692,316
App. No.
17/784,835
Filed
Jun 13, 2022
Granted
Jul 28, 2026
Kind
B2
Art Unit
1644
USPC
530/387.3
Abstract

The present invention provides antibodies to canine IL-4 receptor alpha that have a high binding affinity for canine IL-4 receptor alpha, and that can block the binding of canine IL-4 and/or IL-13 to canine IL-4 receptor alpha. The present invention further relates to epitopes of canine IL-4 receptor alpha that bind to the antibodies to canine IL-4 receptor alpha. The present invention further provides the use of the antibodies for the treatment of atopic dermatitis in dogs.

Claims (26)

1 . An isolated mammalian antibody or antigen binding fragment thereof that binds canine interleukin-4 receptor α (IL-4R α ) comprising a set of six complementary determining regions (CDRs), three of which are heavy chain CDRs: a CDR heavy 1 (HCDR1), a CDR heavy 2 (HCDR2), and a CDR heavy 3 (HCDR3) and three of which are light chain CDRs: a CDR light 1 (LCDR1), a CDR light 2 (LCDR2), and a CDR light 3 (LCDR3); wherein

(i) the HCDR1 comprises the amino acid sequence of SEQ ID NO: 12;

(ii) the HCDR2 comprises the amino acid sequence of SEQ ID NO: 14;

(iii) the HCDR3 comprises the amino acid sequence of SEQ ID NO: 16;

(iv) the LCDR1 comprises the amino acid sequence of SEQ ID NO: 18;

(v) the LCDR2 comprises the amino acid sequence of SEQ ID NO: 20; and

(vi) the LCDR3 comprises the amino acid sequence of SEQ ID NO: 22.

2 . The isolated mammalian antibody or antigen binding fragment thereof of claim 1 , wherein the antibody and antigen binding fragment thereof bind canine IL-4Ra and block the binding of canine IL-4Ra to canine interleukin-4.

3 . The isolated mammalian antibody or antigen binding fragment thereof of claim 1 , that is a caninized antibody or a caninized antigen binding fragment thereof.

4 . The caninized antibody or caninized antigen binding fragment thereof of claim 3 , comprising a hinge region comprising the amino acid sequence selected from the group consisting of SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, and SEQ ID NO: 9.

5 . The caninized antibody or caninized antigen binding fragment thereof of claim 3 , comprising a heavy chain comprising a modified canine IgG-B (IgG-Bm) comprising the amino acid sequence of SEQ ID NO: 10.

6 . The caninized antibody or caninized antigen binding fragment thereof of claim 5 , comprising a heavy chain comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 40, SEQ ID NO: 41, and SEQ ID NO: 42.

7 . An isolated caninized mammalian antibody or caninized antigen binding fragment thereof that binds canine interleukin-4 receptor α (IL-4R α ), comprising a light chain comprising the amino acid sequence SEQ ID NO: 39 and a heavy chain comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 40, SEQ ID NO: 41, and SEQ ID NO: 42.

8 . An isolated caninized mammalian antibody or caninized antigen binding fragment thereof that binds canine interleukin-4 receptor α (IL-4R α ), comprising a light chain comprising the amino acid sequence SEQ ID NO: 44 and a heavy chain comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 40, SEQ ID NO: 41, and SEQ ID NO: 42.

9 . An isolated nucleic acid that encodes the heavy chain of the caninized antibody or caninized antigen binding fragment thereof of claim 3 .

10 . An isolated nucleic acid that encodes the light chain of the caninized antibody or caninized antigen binding fragment thereof of claim 3 .

11 . An expression vector comprising the isolated nucleic acid of claim 9 .

12 . A host cell comprising the expression vector of claim 11 .

13 . A pharmaceutical composition comprising the caninized antibody or caninized antigen binding fragment thereof of claim 3 , and a pharmaceutically acceptable carrier or diluent.

14 . A method of aiding in the blocking of inflammation associated with atopic dermatitis, comprising administering to a subject in need thereof a therapeutically effective amount of the pharmaceutical composition of claim 13 .

15 . An expression vector comprising the isolated nucleic acid of claim 10 .

16 . A host cell comprising the expression vector of claim 15 .

17 . A pharmaceutical composition comprising the caninized antibody or caninized antigen binding fragment thereof of claim 8 , and a pharmaceutically acceptable carrier or diluent.

18 . A method of aiding in the blocking of inflammation associated with atopic dermatitis, comprising administering to a subject in need thereof a therapeutically effective amount of the pharmaceutical composition of claim 17 .

19 . A pharmaceutical composition comprising the caninized antibody or caninized antigen binding fragment thereof of claim 7 , and a pharmaceutically acceptable carrier or diluent.

20 . A method of aiding in the blocking of inflammation associated with atopic dermatitis, comprising administering to a subject in need thereof a therapeutically effective amount of the pharmaceutical composition of claim 19 .

Assignments (5)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 16, 2026
From: MORSEY, MOHAMAD; ZHANG, YUANZHENG
To: INTERVET INC.
Reel/Frame 074982/0766 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 16, 2026
From: MORSEY, MOHAMAD; ZHANG, YUANZHENG
To: INTERVET INC.
Reel/Frame 074982/0775 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 16, 2026
From: MORSEY, MOHAMAD; ZHANG, YUANZHENG
To: INTERVET INC.
Reel/Frame 074982/0813 →
CHANGE OF ADDRESS Recorded Sep 26, 2023
From: INTERVET INC.
To: INTERVET INC.
Reel/Frame 065028/0818 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 15, 2022
From: MORSEY, MOHAMAD; ZHANG, YUANZHENG
To: INTERVET INC.
Reel/Frame 060213/0174 →
Continuity (5)
Provisional Application 63015220 · Apr 24, 2020
Provisional Application 63015209 · Apr 24, 2020
Provisional Application 62951778 · Dec 20, 2019
Provisional Application 62951793 · Dec 20, 2019
Related Publication 20230053131A1 · Feb 16, 2023
References Cited (33)
US 4816567A · Cabilly et al. · 1989 [cited by applicant]
US 7208579B2 · Watson et al. · 2007 [cited by applicant]
US 8790651B2 · Bammert et al. · 2014 [cited by applicant]
US 10093731B2 · Li et al. · 2018 [cited by applicant]
US 10106607B2 · Morsey et al. · 2018 [cited by applicant]
US 20150017176A1 · Kostic et al. · 2015 [cited by applicant]
US 20180346580A1 · Morsey et al. · 2018 [cited by applicant]
US 20180371097A1 · Morsey et al. · 2018 [cited by applicant]
US 20230044037A1 · Morsey · 2023 [cited by examiner]
US 20230250177A1 · Morsey · 2023 [cited by examiner]
US 20230295289A1 · Morsey · 2023 [cited by examiner]
CN 107683291A · 2018 [cited by applicant]
JP 2018511322A · 2018 [cited by applicant]
RU 2679920C2 · 2019 [cited by applicant]
WO WO2014197470A1 · 2014 [cited by applicant]
WO 2016156588A1 · 2016 [cited by applicant]
WO 2017102920A1 · 2017 [cited by applicant]
Ahmed et al., 2015, “Identification and Characterization of a Novel IL-4 Receptor α Chain (IL-4Rα) Antagonist to Inhibit IL-4 Signalling,” Cell Physiol. Biochem., 36(3):831-842. [cited by applicant]
Bergeron et al., Comparative functional characterization of canine IgG subclasses, Veterinary Immunology and Immunopathology, 2014, pp. 31-41, 157. [cited by applicant]
Chothia and Lesk et al, Canonical Structures for the Hypervariable Regions of Immunoglobins, J. Mol. Biol., 1987, 901-917, 196. [cited by applicant]
Chothia et al., Conformations of immunoglobin hypervariable regions, Nature, 1989, 877-883, 342. [cited by applicant]
Gelebart, Pascal and Lai, Raymond, IL22RA1 (interleukin 22 receptor, alpha 1), Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2010, 1106-1110, 14(12). [cited by applicant]
Harskamp et al., Immunology of Atopic Dermatitis: Novel Insights into Mechanisms and Immunomodulatory Therapies, Seminars in Cutaneous Medicine and Surgery, 2013, 132-139, 32. [cited by applicant]
Huber, Samuel et al., IL-22BP is regulated by the inflammasome and modulates tumorigenesis in the intestine, Nature, 2012, 259-263, 491. [cited by applicant]
Kabat, the Structural Basis of Antibody Complementarity, Adv. Prot. Chem., 1978, 1-75, 32. [cited by applicant]
Kabat, Unusual Distributions of Amino Acids in Complementarity-determining (Hypervriable) Segment of Heavy and Light Chains of Immunoglobulins and Their Possible Roles in Specificity of Antibody-combining Sites, J. Biol… [cited by applicant]
Lee, Donna W. et al., Nonclinical safety assessment of a human interleukin-22FC IG fusion protein demonstrates in vitro to in vivo and cross-species translatability, Pharmacol Res Perspect., 2018, 1-13, e00434. [cited by applicant]
Morrison, Sherie L. et al., Chimeric human antibody molecules: Mouse antigen-binding domains with human constant region domains, Proc. Natl. Acad. Sci. USA, 1984, 6851-6855, 81. [cited by applicant]
Nuttall et al., Canine Atopic Dermatitis—what have we learned?, Veterinary Record, 2013, 201-207, 172(8). [cited by applicant]
Rahman et al., The Pathology and Immunology of Atopic Dermatitis, Inflammation & Allergy—Drug Targets, 2011, 186-496, 10. [cited by applicant]
Ruzicka, Thomas et al., Anti-Interleukin-31 Receptor A Antibody for Atopic Dermatitis, The New England Journal of Medicine, 2017, 826-835, 376(9). [cited by applicant]
Tang et al., Cloning and characterization of cDNAs encoding four different canine immunoglobulin Y chains, Veterinary Immunology and Immunopathology, 2001, pp. 259-270, 80. [cited by applicant]
Xu, Wenfeng et al., A soluble class II cytokine receptor, IL-22RA2, is a naturally occurring IL-22 antagonist, PNAS, 2001, 9511-9516, vol. 98 | No. 17. [cited by applicant]