Mitochondrial markers of neurodegenerative diseases
US-2022049307-A1 · Feb 17, 2022 · US
US12509525B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12509525-B2 |
| Application number | US-202017632191-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 3, 2020 |
| Priority date | Aug 2, 2019 |
| Publication date | Dec 30, 2025 |
| Grant date | Dec 30, 2025 |
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The present invention provides therapeutics for the treatment of Multiple myeloma. In particular, the present invention provides chimeric antigen receptor (CAR) T-cells that can target the B cell maturation antigen.
Opening claim text (preview).
The invention claimed is: 1 . A chimeric antigen receptor (CAR) comprising an extracellular domain comprising a BCMA targeting-moiety, a transmembrane domain, and an intracellular signaling domain, wherein the BCMA-targeting moiety comprises a VH domain and a VL domain, wherein said VH domain and VL domain consist, respectively, of SEQ ID NO: 1 and SEQ ID NO: 2. 2 . The chimeric antigen receptor of claim 1 , wherein the BCMA-targeting moiety comprises SEQ ID NO: 3. 3 . A chimeric antigen receptor (CAR) comprising an extracellular domain comprising a BCMA targeting-moiety, a transmembrane domain, and an intracellular signaling domain, wherein the BCMA-targeting moiety is a single-chain variable fragment, comprising a VL domain and a VH domain, wherein said VH and VL domains respectively comprise SEQ ID NO: 1 and SEQ ID NO: 2. 4 . The chimeric antigen receptor of claim 3 , wherein the chimeric antigen receptor comprises: a. the single-chain variable fragment, comprising a VL domain and a VH domain, wherein said VH and VL domains respectively comprise SEQ ID NO: 1 and SEQ ID NO: 2; b. the transmembrane domain bound to a Hinge domain comprising SEQ ID NO: 9; c. a costimulatory signaling domain comprising SEQ ID NO: 11; and d. the intracellular signaling domain comprising SEQ ID NO: 10. 5 . The chimeric antigen receptor (CAR) of claim 4 , wherein the CAR consists of SEQ ID NO: 13. 6 . A nucleic acid encoding the chimeric antigen receptor according to claim 3 . 7 . A cell comprising the nucleic acid according to claim 6 . 8 . The cell according to claim 7 , wherein the cell is a T-cell. 9 . A nucleic acid encoding the chimeric antigen receptor according to claim 1 . 10 . A cell comprising the nucleic acid according to claim 9 . 11 . The cell according to claim 10 , wherein the cell is a T-cell. 12 . A pharmaceutical composition comprising a plurality of cells according to claim 10 and a pharmaceutically acceptable carrier or diluent. 13 . A method of treating multiple myeloma, wherein the method comprises administering the cell of claim 10 , or a pharmaceutical composition comprising the cell, to a patient in need thereof. 14 . The method of claim 13 , wherein the cell is a T-cell. 15 . An immunoglobulin binding protein comprising a BCMA targeting-moiety, wherein the BCMA-targeting moiety comprises a VH domain and a VL domain, wherein said VH domain and VL domain consist, respectively, of SEQ ID NO: 1 and SEQ ID NO: 2. 16 . The immunoglobulin binding protein of claim 15 , wherein the BCMA-targeting moiety comprises SEQ ID NO: 3. 17 . The immunoglobulin binding protein of claim 15 , wherein the BCMA-targeting moiety is an antibody, a single-chain variable fragment, an antigen-binding fragment, a single-chain antigen-binding fragment, or a single-chain fusion protein.
Receptors for tumor necrosis factors [TNF], e.g. lymphotoxin receptor [LTR], CD30 · CPC title
Chimeric antigen receptors [CAR] · CPC title
T-cells, e.g. tumour infiltrating lymphocytes [TIL] or regulatory T [Treg] cells; Lymphokine-activated killer [LAK] cells · CPC title
characterised by the cancer treated · CPC title
containing a transmembrane segment · CPC title
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