US2023151092A1PendingUtilityA1
CD229 Car T Cells And Methods Of Use Thereof
Est. expiryJul 20, 2036(~10 yrs left)· nominal 20-yr term from priority
G01N 33/57557G01N 33/5758A61K 40/4261A61K 40/4224A61K 40/4215A61K 40/4211A61K 40/31A61K 40/11C12N 5/0636C07K 2319/03C07K 14/705C07K 14/70578C07K 2319/00C07K 14/7051C07K 2317/622C07K 2319/33C07K 2317/73C07K 2319/02C07K 2317/565C07K 2317/33C07K 2317/21C07K 2317/732C07K 2317/55C07K 14/70596C07K 16/2803A61K 38/1774C07K 2317/734C07K 2319/30A61P 35/00C12N 2510/00C07K 2317/53C07K 2317/52C07K 14/70517A61K 45/06C07K 2319/42C07K 2317/76A61K 38/177A61K 39/3955C07K 14/70521G01N 33/57407A61K 35/17A61K 39/001111G01N 33/6854A61K 2039/5156A61K 2039/5158A61K 2039/505G01N 2333/70503
61
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
Disclosed are chimeric antigen receptor (CAR) polypeptides comprising a CD229 antigen binding domain, a transmembrane domain, and an intracellular signaling domain. Disclosed are nucleic acid sequences capable of encoding a CAR polypeptide comprising a CD229 antigen binding domain, a transmembrane domain, and an intracellular signaling domain. Also disclosed are vectors and cells comprising one or both of the CAR polypeptides and nucleic acid sequences capable of encoding CAR polypeptides. Also disclosed are methods of treating.
Claims
exact text as granted — not AI-modified1 . A chimeric antigen receptor (CAR) polypeptide, comprising a CD229 antigen binding domain, a transmembrane domain, and an intracellular signaling domain.
2 . The CAR polypeptide of claim 1 , wherein the intracellular signaling domain comprises a co-stimulatory signaling region.
3 . The CAR polypeptide of claim 2 , wherein the co-stimulatory signaling region comprises the cytoplasmic domain of a costimulatory molecule selected from the group consisting of CD27, CD28, 4-1BB, OX40, CD30, CD40, PD-1, ICOS, lymphocyte function-associated antigen-1 (LFA-1), CD2, CD7, LIGHT, NKG2C, B7-H3, a ligand that specifically binds with CD83, and any combination thereof.
4 . The CAR polypeptide of claim 1 , wherein the intracellular signaling domain is a T cell signaling domain.
5 . The CAR polypeptide of claim 1 , wherein the intracellular signaling domain comprises a CD3 zeta (CD3ζ) signaling domain.
6 . The CAR polypeptide of claim 1 , wherein the intracellular signaling domain comprises a CD3ζ signaling domain and a co-stimulatory signaling region, wherein the co-stimulatory signaling region comprises the cytoplasmic domain of CD28 or 4-1BB.
7 . The CAR polypeptide of claim 1 , wherein the CD229 antigen binding domain is an antibody fragment or an antigen-binding fragment that specifically binds to CD229.
8 . The CAR polypeptide of claim 6 , wherein the CD229 antigen binding domain is a Fab or a single-chain variable fragment (scFv) of an antibody that specifically binds CD229.
9 . The CAR polypeptide of claim 1 , wherein the CD229 antigen binding domain comprises an amino acid sequence set forth in SEQ ID NO:1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, or 15.
10 . The CAR polypeptide of claim 1 , wherein the CD229 antigen binding domain comprises a variable heavy chain comprising a sequence having at least 90% identity a sequence set forth in SEQ ID NOs:16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, or 30.
11 . The CAR polypeptide of claim 1 , wherein the CD229 antigen binding domain comprises a variable light chain comprising a sequence having at least 90% identity a sequence set forth in SEQ ID NOs:31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, or 45.
12 . The CAR polypeptide of claim 1 , wherein the CD229 antigen binding domain comprises a heavy chain immunoglobulin variable region comprising:
a. a complementarity determining region 1 (CDR1) comprising the sequence of SEQ ID NO:46, 49, 52, 57, 60, 63, 66, 69, 71, 74, 77, 80, 83 or 86; b. a CDR2 comprising the sequence of SEQ ID NO:47, 50, 53, 55, 58, 61, 64, 67, 70, 72, 75, 78, 81, 84, or 87; and c. a CDR3 comprising the sequence of SEQ ID NO:48, 51, 54, 56, 59, 62, 65, 68, 71, 73, 76, 79, 82, 85, or 88.
13 . The CAR polypeptide of claim 1 , wherein the CD229 antigen binding domain comprises a light chain immunoglobulin variable region comprising:
a. a complementarity determining region 1 (CDR1) comprising the sequence of SEQ ID NO:89, 91, 93, 95, 97, 99, 101, 103, 105, 107, 109, 111, 113, 115, or 117; b. a CDR2 comprising the sequence of DAS, DVS, GGS, EDN, AAS, DDD, or AAS; and c. a CDR3 comprising the sequence of SEQ ID NO:90, 92, 94, 96, 98, 100, 102, 104, 106, 108, 110, 112, 114, 116, or 118.
14 . The CAR polypeptide of claim 1 , wherein the transmembrane domain comprises an immunoglobulin Fc domain.
15 . (canceled)
16 . The CAR polypeptide of claim 1 , wherein the transmembrane domain comprises a CD8α domain, CD3ζ, FcεR1γ, CD4, CD7, CD28, OX40, or H2-Kb.
17 .- 22 . (canceled)
23 . A nucleic acid sequence capable of encoding the CAR polypeptide of claim 1 .
24 .- 33 . (canceled)
34 . A T cell expressing the CAR polypeptide of claim 1 .
35 . (canceled)
36 . (canceled)
37 . An antibody or fragment thereof that binds to human CD229, wherein said antibody comprises a variable heavy chain comprising a sequence having at least 90% identity to a sequence set forth in SEQ ID NOs:16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, or 30 and/or a variable light chain comprising a sequence having at least 90% identity to a sequence set forth in SEQ ID NOs:31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, or 45.
38 .- 46 . (canceled)
47 . A method of treating multiple myeloma comprising administering an effective amount of a T cell genetically modified to express the CAR polypeptide of claim 1 to a subject in need thereof.
48 .- 52 . (canceled)
53 . A method of killing CD229 positive cells comprising administering an effective amount of a T cell genetically modified to express the CAR polypeptide of claim 1 to a sample comprising CD229 positive cells.
54 .- 57 . (canceled)Join the waitlist — get patent alerts
Track US2023151092A1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.