IP Library › Granted Patent US 12,559,555
Granted Patent B2
US 12,559,555 · App. 17/905,943 · Granted Feb 24, 2026

Anti-LILRB4 antibodies and derivative products

Inventors: An Song (Palo Alto, CA); Tao Huang (Mountain View, CA); Ryan Stafford (Foster City, CA); Maria Jose Costa (Palo Alto, CA); Kyu Hee Hong (Palo Alto, CA); Caroline Bonnans (San Francisco, CA); Jianhui Zhou (Redwood City, CA); Li Zhou (San Jose, CA); Ji Li (Foster City, CA); J. Paul Woodard (Palo Alto, CA); X. Charlene Liao (Palo Alto, CA)
C07K16/2803A61K38/177A61K38/1774A61K39/3955A61K40/11A61K40/24A61K40/31A61K40/4203A61K45/06A61P35/02C07K14/7051C07K14/70517C07K14/70521C07K14/70578C07K16/2809C12N5/0636A61K2039/505A61K2239/21A61K2239/22A61K2239/29C07K2317/24C07K2317/31C07K2317/622C07K2317/73C07K2317/732C07K2317/92C07K2319/02C07K2319/03C07K2319/33
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Quick Facts
Patent No.
US 12,559,555
App. No.
17/905,943
Granted
Feb 24, 2026
Kind
B2
Abstract

The present disclosure provides anti-LILRB4 antibodies or antigen-binding fragments thereof, anti-LILRB4 chimeric antigen receptor protein, isolated polynucleotides encoding the same, pharmaceutical compositions comprising the same, and the uses thereof.

Claims (24)

1 . An isolated anti-Leukocyte Immunoglobulin-like subfamily B member 4 (anti-LILRB4) antibody or an antigen-binding fragment thereof, comprising:

a) a heavy chain variable region comprising a heavy chain complementarity determining region (HC-CDR) 1 having an amino acid sequence of SEQ ID NO: 5, an HC-CDR2 having an amino acid sequence of SEQ ID NO: 6 and an HC-CDR3 having an amino acid sequence of SEQ ID NO: 7; and

b) a light chain variable region comprising a light chain complementarity determining region (LC-CDR) 1 having an amino acid sequence of SEQ ID NO: 8 with a mutation at amino acid residues NS, an LC-CDR2 having an amino acid sequence of SEQ ID NO: 9 and an LC-CDR3 having an amino acid sequence of SEQ ID NO: 10.

2 . The antibody or antigen-binding fragment thereof of claim 1 , wherein the LC-CDR1 has the amino acid sequence of SEQ ID NO: 28.

3 . The antibody or antigen-binding fragment thereof of claim 1 , wherein the heavy chain variable region has the amino acid sequence of SEQ ID NO: 1; and wherein the light chain variable region has the amino acid sequence of SEQ ID NO: 27.

4 . The antibody or antigen-binding fragment thereof of claim 1 , further comprising an immunoglobulin constant region, optionally a constant region of Ig, or optionally a constant region of human IgG.

5 . The antibody or antigen-binding fragment thereof of claim 1 , which is humanized.

6 . The antibody or antigen-binding fragment thereof of claim 1 , which is a camelized single domain antibody, a diabody, a scFv, a scFv dimer, a BsFv, a dsFv, a (dsFv) 2 , a dsFv-dsFv′, an Fv fragment, a Fab, a Fab′, a F(ab′) 2 , a bispecific antibody, a ds diabody, a nanobody, a domain antibody, or a bivalent antibody, wherein the bispecific antibody is an antibody against LILRB4 and CD3.

7 . The antibody or antigen-binding fragment thereof of claim 1 linked to one or more conjugate moieties, wherein the conjugate moiety comprises a clearance-modifying agent, a toxin, a detectable label, a chemotherapeutic agent, a cytokine, or a purification moiety.

8 . A pharmaceutical composition comprising the antibody or antigen-binding fragment thereof of claim 1 , and a pharmaceutically acceptable carrier.

9 . An isolated polynucleotide encoding the antibody or antigen-binding fragment thereof of claim 1 .

10 . A vector comprising the isolated polynucleotide of claim 9 .

11 . A host cell comprising the vector of claim 10 .

12 . A method of expressing the antibody or antigen-binding fragment thereof, comprising culturing the host cell of claim 11 under the condition at which the vector is expressed.

13 . A chimeric antigen receptor (CAR) protein, comprising:

a) a heavy chain variable region comprising an HC-CDR1 having an amino acid sequence of SEQ ID NO: 5, an HC-CDR2 having an amino acid sequence of SEQ ID NO: 6 and an HC-CDR3 having an amino acid sequence of SEQ ID NO: SEQ ID NO: 7; and

b) a light chain variable region comprising an LC-CDR1 having an amino acid sequence of SEQ ID NO: 8 with a mutation at amino acid residues NS, an LC-CDR2 having an amino acid sequence of SEQ ID NO: 9 and an LC-CDR3 having an amino acid sequence of SEQ ID NO: 10.

14 . The CAR protein of claim 13 , wherein the LC-CDR1 has the amino acid sequence of SEQ ID NO: 28.

15 . The CAR protein of claim 13 , wherein the heavy chain variable region has an amino acid sequence of SEQ ID NO: 1; and wherein the light chain variable region has an amino acid sequence of SEQ ID NO: 27.

16 . The CAR protein of claim 13 , comprising a single-chain variable fragment (scFv) having an amino acid sequence identical to SEQ ID NOS: 66 or 68.

17 . The CAR protein of claim 13 , further comprising a CD8a transmembrane domain or a CD28 transmembrane domain.

18 . The CAR protein of claim 13 , further comprising a 4-1BB intracellular co-stimulatory signaling domain, a CD28 intracellular co-stimulatory signaling domain or a CD3ζ intracellular T cell signaling domain.

19 . A polynucleotide molecule encoding a CAR protein according to claim 13 .

20 . An engineered cell comprising the polynucleotide molecule of claim 19 , wherein the cell is a T cell, an NK cell or a macrophage.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 16, 2022
From: SONG, AN; HUANG, TAO; STAFFORD, RYAN; COSTA, MARIA JOSE; HONG, KYU HEE; BONNANS, CAROLINE; ZHOU, JIANHUI; ZHOU, LI; LI, JI; WOODARD, J. PAUL; LIAO, X. CHARLENE
To: IMMUNE-ONC THERAPEUTICS, INC.
Reel/Frame 062118/0778 →
Continuity (2)
Provisional Application 62988892 · Mar 12, 2020
Related Publication 20230340114A1 · Oct 26, 2023
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