US2019144521A1PendingUtilityA1
T cell receptors
Est. expiryApr 8, 2036(~9.7 yrs left)· nominal 20-yr term from priority
A61K 38/00A61P 35/00C07K 14/4748C07K 14/7051A61K 35/17A61K 40/4268A61K 40/11A61K 40/32C12N 5/0636A61K 39/001111C12N 2510/00
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Claims
Abstract
The present invention relates to T cell receptors (TCRs) which bind the HLA-A*0201 restricted peptide GVYDGEEHSV (SEQ ID NO: 1) derived from the MAGE-B2 protein. The TCRs of the invention demonstrate excellent specificity profiles for this MAGE epitope. Also provided are nucleic acids encoding the TCRs, cells engineered to present the TCRs, cells harbouring expression vectors encoding the TCRs and pharmaceutical compositions comprising the TCRs, nucleic acids or cells of the invention.
Claims
exact text as granted — not AI-modified1 . A T cell receptor (TCR) having the property of binding to GVYDGEEHSV (SEQ ID No: 1) in complex with HLA-A*0201 AND GVYDGREHTV (SEQ ID No 2) in complex with HLA-A*0201 with a dissociation constant of from about 0.05 μM to about 20.0 μM when measured with surface plasmon resonance at 25° C. and at a pH between 7.1 and 7.5 using a soluble form of the TCR, wherein the TCR comprises a TCR alpha chain variable domain and a TCR beta chain variable domain, and wherein the TCR variable domains form contacts with at least residues V2, Y3 and D4 of GVYDGEEHSV (SEQ ID No: 1).
2 . A TCR according to claim 1 , which is an alpha-beta heterodimer, having an alpha chain TRAV10+TRAC constant domain sequence and a beta chain TRBV24-1+TRBC-2 constant domain sequence.
3 . A TCR as claimed in claim 1 , which is in single chain format of the type Vα-L-Vβ, Vβ-L-Vα, Vα-Cα-L-Vβ, or Vα-L-Vβ-Cβ, wherein Vα and Vβ are TCR α and β variable regions respectively, Cα and Cβ are TCR α and β constant regions respectively, and L is a linker sequence.
4 . A TCR as claimed in claim 1 , which is associated with a detectable label, a therapeutic agent or a PK modifying moiety.
5 . A TCR as claimed in claim 1 , wherein the alpha chain variable domain comprises an amino acid sequence that has at least 80% identity to the amino acid sequence of the alpha chain variable domain of a TCR of the invention which may have the following mutation:
CDR2 M4
V
CDR3 S4
T
CDR3 S4
N
with reference to the numbering shown in SEQ ID No: 3, and/or
the beta chain variable domain of a TCR of the invention which may have at least one of the following mutations:
CDR2 S1
A
CDR3 S4
T
CDR3 N10
E
CDR3 N10
G
CDR3 N10
V
with reference to the numbering shown in SEQ ID No: 4.
6 . A TCR as claimed in claim 1 , wherein the alpha chain variable domain comprises the amino acid sequence of amino acid residues 1-105 of SEQ ID No: 3 or 7-9 or
an amino acid sequence in which amino acid residues 1-27, 34-47, and 54-90 thereof have at least 90% or 95% identity to the sequence of amino acid residues 1-27, 34-47, and 54-90 respectively of SEQ ID No: 3 or 7-9 and in which amino acid residues 28-34, 48-53 and 91-105 have at least 90% or 95% identity to the sequence of amino acid residues 28-33, 48-53 and 91-105 respectively of SEQ ID No 3 or 7-9.
7 . A TCR as claimed in claim 1 , wherein the alpha chain variable domain comprises the amino acid sequence of amino acid residues 1-105 of SEQ ID No: 7-9 or an amino acid sequence in which amino acid residues 1-27, 34-47 and 55-89 thereof have at least 90% or 95% identity to the sequence of amino acid residues 1-27, 34-47, and 55-89 respectively of SEQ ID No: 7-9 and in which amino acid residues 28-33, 48-53 and 91-105 have at least 90% or 95% identity to the sequence of amino acid residues 28-33, 48-53 and 91-105 respectively of SEQ ID No: 7-9.
8 . A TCR as claimed in claim 1 , wherein in the alpha chain variable domain the sequence of
(i) amino acid residues 1-27 thereof has (a) at least 90% identity to the sequence of amino acid residues 1-26 of SEQ ID No: 3 or (b) has one, two or three amino acid residues inserted or deleted relative to the sequence of (a); (ii) amino acid residues 28-33 is VSPFSN; (iii) amino acid residues 34-47 thereof has (a) at least 90% identity to the sequence of amino acid residues 34-47 of SEQ ID NO: 3 or (b) has one, two or three amino acid residues inserted or deleted relative to the sequence of (a); (iv) amino acid residues 48-53 is LTIMTF or LMIVTF; (v) amino acid residues 54-90 thereof has at least 90% identity to the sequence of amino acid residues 55-89 of SEQ ID No: 3 or has one, two or three insertions, deletions or substitutions relative thereto; (vi) amino acids 91-105 is CVVSGGTDSWGKLQF or CVVTGGTDSWGKLQF.
9 . A TCR as claimed in claim 1 , wherein the beta chain variable domain comprises the amino acid sequence of SEQ ID No: 4 or 10-12 or an amino acid sequence in which amino acid residues 1-45, 51-67, and 74-109 thereof have at least 90% or 95% identity to the sequence of amino acid residues 1-45, 51-67, and 74-109 respectively of SEQ ID No: 4 or 10-12 and in which amino acid residues 46-50, 68-73 and 109-123 have at least 90% or 95% identity to the sequence of amino acid residues 46-50, 68-73 and 109-123 respectively of SEQ ID No: 4 or 10-12.
10 . A TCR according to claim 1 , wherein in the beta chain variable domain the sequence of
(i) amino acid residues 1-45 thereof has (a) at least 90% identity to the amino acid sequence of residues 1-26 of SEQ ID No: 4 or (b) has one, two or three amino acid residues inserted or deleted relative to the sequence of (a); (ii) amino acid residues 46-50 is KGHDR or KGRDR, (iii) amino acid residues 51-67 thereof has (a) at least 90% identity to the sequence of amino acid residues 51-67 of SEQ ID NO: 4 or (b) has one, two or three amino acid residues inserted or deleted relative to the sequence of (a); (iv) amino acid residues 68-73 is SFDVK; (v) amino acid residues 54-90 thereof has (a) at least 90% identity to the sequence of amino acid residues 54-90 of SEQ ID NO: 4 or (b) has one, two or three amino acid residues inserted or deleted relative to the sequence of (a); (vi) amino acids 109-123 is CATSGQGAYNEQFF or CATNGQGAYREQFF or CATSGQGAYGEQFF CATSGQGAYVEQFF.
11 . A nucleic acid encoding the TCR as claimed in claim 1 .
12 . An isolated or non-naturally occurring cell, especially a T-cell, presenting a TCR as claimed in claim 1 .
13 . A cell harboring
(a) a TCR expression vector which comprises the nucleic acid as claimed in claim 11 in a single open reading frame, or two distinct open reading frames encoding the alpha chain and the beta chain respectively; or (b) a first expression vector which comprises nucleic acid encoding the alpha chain of a TCR as claimed in claim 1 , and a second expression vector which comprises nucleic acid encoding the beta chain of a TCR as claimed in claim 1 .
14 . A pharmaceutical composition comprising the TCR as claimed in claim 1 , together with one or more pharmaceutically acceptable carriers or excipients.
15 . A pharmaceutical composition comprising the nucleic acid of claim 11 , together with one or more pharmaceutically acceptable carriers or excipients.
16 . A pharmaceutical composition comprising the cell as claimed in claim 12 , together with one or more pharmaceutically acceptable carriers or excipients.
17 . A method of treating cancer comprising administering the TCR of claim 1 .
18 . A method of treating cancer comprising administering the nucleic acid of claim 11 .
19 . A method of treating cancer comprising administering the cell of claim 12 .Join the waitlist — get patent alerts
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