US2024025962A1PendingUtilityA1
Compositions and methods for treating cancer with duocars
Est. expirySep 2, 2036(~10.1 yrs left)· nominal 20-yr term from priority
A61K 35/17A61K 40/50A61K 40/15A61K 40/42A61K 2239/29A61K 2239/28A61K 2239/13A61K 40/4221A61K 40/4212A61K 40/4211A61K 40/31A61K 40/11A61K 2239/48A61K 39/001112A61K 39/001124C07K 14/7051C07K 14/70517C07K 14/70578C07K 16/2803C07K 16/2887A61P 35/02C07K 14/70521C12N 15/85C07K 2317/622C07K 2319/03C07K 2317/31C07K 2319/00C07K 2319/02C07K 2319/75A61K 2039/5156C07K 16/2827C07K 2319/33C12N 2840/20A61P 35/00C12N 15/86C12N 2740/16043C12N 2740/16071C12N 2800/40A61K 2039/804
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Claims
Abstract
Novel therapeutic immunotherapy compositions comprising at least two vectors, each vector encoding a functional CAR, whereby the combination of vectors results in the expression of two or more non-identical binding domains, wherein each vector encoded binding domain(s) are covalently linked to a transmembrane domain and one or more non-identical intracellular signaling motifs are provided herein as well as are methods of use of same in a patient-specific immunotherapy that can be used to treat cancers and other diseases and conditions.
Claims
exact text as granted — not AI-modified1 - 37 . (canceled)
38 . A method of treating a subject having an autoimmune disease, the method comprising administering to the subject having the autoimmune disease a pharmaceutical composition comprising an antitumor effective amount of a population of human T cells,
wherein the population of human T-cells are autologous to the subject, and wherein each cell of the population of human T-cells comprises at least one multi-cistronic vector, each of the at least one multi-cistronic vector comprises a promoter operably linked to a multi-cistronic nucleic acid sequence encoding two or more functional CARs, wherein at least one of the two or more functional CARs comprises SEQ ID NO: 50, and thereby treating the subject having the autoimmune disease.
39 . The method of claim 38 , wherein the population of human T-cells are infused directly into the subject.
40 . The method of claim 38 , wherein the autoimmune disease is multiple sclerosis.
41 . The method of claim 38 , wherein the autoimmune disease is a graft-versus-host disease.
42 . The method of claim 38 , wherein the autoimmune disease is a skin allergy.
43 . The method of claim 38 , wherein the autoimmune disease is a CD19+ autoimmune disease.
44 . The method of claim 38 , wherein the population of human T-cells are T-regulatory cells.
45 . The method of claim 38 , wherein the population of human T-cells are T helper 2 (Th-2 cells).
46 . The method of claim 38 , wherein the population of human T-cells are T cells that promote a Th-2-like immune response.Cited by (0)
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