US2020016203A1PendingUtilityA1
Cell
Est. expiryNov 21, 2033(~7.4 yrs left)· nominal 20-yr term from priority
A61P 35/02A61P 37/08A61P 35/00C07K 14/70589C12Y 301/03048A61P 37/06A61P 37/02C07K 14/7051C07K 2319/03C07K 2317/52C07K 2317/622C07K 2319/74C07K 16/2803C12N 9/16A61K 38/00C12N 2740/15043C07K 14/70521C12N 15/86C07K 14/70503C07K 14/70517C07K 2319/01C07K 2319/02C12N 2510/00C12N 2740/10043C12N 5/0638A61K 35/17C12N 5/0637A61K 2039/5158C12N 5/0636C12N 5/0646A61K 39/0011A61K 2239/17A61K 40/4221A61K 2239/28A61P 31/12C12N 15/85A61K 40/11A61K 40/4211A61K 40/4224A61K 40/31A61K 2239/13A61K 40/4202
69
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Claims
Abstract
The present invention provides a cell which co-expresses a first chimeric antigen receptor (CAR) and second CAR at the cell surface, each CAR comprising: (i) an antigen-binding domain; (ii) a spacer (iii) a trans-membrane domain; and (iv) an endodomain wherein the antigen binding domains of the first and second CARs bind to different antigens, and wherein one of the first or second CARs is an activating CAR comprising an activating endodomain and the other CAR is an inhibitory CAR comprising a ligation-off inhibitory endodomain.
Claims
exact text as granted — not AI-modified1 . A T cell which co-expresses a first chimeric antigen receptor (CAR) and second CAR at the cell surface, each CAR comprising:
(i) an antigen-binding domain; (ii) a spacer (iii) a trans-membrane domain; and (iv) an endodomain wherein the antigen binding domains of the first and second CARs bind to different antigens, and wherein one of the first or second CARs is an activating CAR comprising an activating endodomain and the other CAR is an inhibitory CAR comprising a ligation-on inhibitory endodomain.
2 - 11 . (canceled)
12 . A nucleic acid sequence encoding both the first and second chimeric antigen receptors (CARs) as defined in claim 1 .
13 . A nucleic acid sequence according to claim 12 , which has the following structure:
AgB1-spacer1-TM1-endo1-coexpr-AbB2-spacer2-TM2-endo2 in which AgB1 is a nucleic acid sequence encoding the antigen-binding domain of the first CAR; spacer 1 is a nucleic acid sequence encoding the spacer of the first CAR; TM1 is a a nucleic acid sequence encoding the transmembrane domain of the first CAR; endo 1 is a nucleic acid sequence encoding the endodomain of the first CAR; coexpr is a nucleic acid sequence enabling co-expression of both CARs AgB2 is a nucleic acid sequence encoding the antigen-binding domain of the second CAR; spacer 2 is a nucleic acid sequence encoding the spacer of the second CAR; TM2 is a a nucleic acid sequence encoding the transmembrane domain of the second CAR; endo 2 is a nucleic acid sequence encoding the endodomain of the second CAR; which nucleic acid sequence, when expressed in a T cell, encodes a polypeptide which is cleaved at the cleavage site such that the first and second CARs are co-expressed at the T cell surface.
14 - 18 . (canceled)
19 . A vector comprising a nucleic acid sequence according to claim 12 .
20 - 22 . (canceled)
23 . A pharmaceutical composition comprising a plurality of T cells according to claim 1 .
24 . A method for treating and/or preventing a disease, which comprises the step of administering a pharmaceutical composition according to claim 23 to a subject.
25 . (canceled)
26 . A method according to claim 24 or 25 , wherein the disease is a cancer.
27 - 28 . (canceled)
29 . A natural killer (NK) cell which co-expresses a first chimeric antigen receptor (CAR) and second CAR at the cell surface, each CAR comprising:
(i) an antigen-binding domain; (ii) a spacer (iii) a trans-membrane domain; and (iv) an endodomain wherein the antigen binding domains of the first and second CARs bind to different antigens, and wherein one of the first or second CARs is an activating CAR comprising an activating endodomain and the other CAR is an inhibitory CAR comprising a ligation-on inhibitory endodomain.
30 . (canceled)Cited by (0)
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