Mutated humanized 12G4 antibodies and the fragments thereof against the human anti-Mullerian hormone receptor type II
Novel mutated humanized 12G4 antibodies, and fragments thereof, directed against the anti-Müllerian hormone type II receptor.
1. A mutated humanized 12G4 monoclonal antibody, comprising or consisting of:
a) a light chain comprising or consisting of:
a variable region (VL) according to amino acid sequence SEQ ID NO: 2 or SEQ ID NO: 4, said VL consisting of three regions determining antigen recognition (CDR) surrounded by four framework regions (FR), and a constant region according to amino acid sequence SEQ ID NO: 6 or a sequence having at least 80% homology with SEQ ID NO: 6, and
b) a heavy chain comprising or consisting of:
a variable region (VH) according to amino acid sequence SEQ ID NO: 8, or SEQ ID NO: 10, and
a constant region according to amino acid sequence of SEQ ID NO: 12 or a sequence having at least 80% homology with SEQ ID NO: 12,
wherein said mutated humanized 12G4 monoclonal antibody comprises at least one mutation selected from the group consisting of:
a mutation located in one of the CDR regions of the VL that is a substitution of at least one amino acid selected from the group consisting of S179P, one of E184K, E184G, or E184D, and S182F,
a mutation located in one of the FR regions of VL that is a substitution of at least one amino acid selected from the group consisting of: I177T, I132T, A1431, 1150A, S158P, L175Q, Y178H, V187A, 51921, G197D, and F212S, and
a mutation located in the heavy chain that is a substitution of at least one amino acid selected from the group consisting of: Q1E, Q3E or Q3R, Q6E, A9T, V11A, K12R, K13R, K19E, V20A, one of A24G, A24V or A24T, Q39E, A40V, S31G, L45P, D56N, A76T, A79T, R87G, T58A, Q62R, V67M, I70N, T74A, S77P, A79T, S88P, E89D, F102S, A1031, L110P, and 51141, and
said mutated humanized 12 G4 monoclonal antibody has a K D for the human anti-Müllerian hormone type II receptor (AMHRII) at least equal to that of the chimeric 12G4 monoclonal antibody, comprising or consisting of:
a) a light chain consisting of:
a variable region according to amino acid sequence SEQ ID NO: 14, and
a constant region according to amino acid sequence SEQ ID NO: 6,
b) a heavy chain consisting of:
a variable region according to amino acid sequence SEQ ID NO: 18, or SEQ ID NO: 10, and
a constant region according to amino acid sequence SEQ ID NO: 12,
for said receptor below 10 −7 M.
2. The mutated humanized 12G4 monoclonal antibody according to claim 1 , wherein said at least one mutation is said substitution in said CDR region.
3. The mutated humanized 12G4 monoclonal antibody according to claim 1 , wherein said at least one mutation is said substitution in said FR regions of VL.
4. The mutated humanized 12G4 monoclonal antibody according to claim 1 , wherein said at least one mutation is said substitution in the heavy chain.
5. The mutated humanized 12G4 monoclonal antibody according to claim 1 , wherein:
a) the light chain comprises or consists of a variable region according to amino acid sequence of SEQ ID NO: 2 in which said at least one substitution in said CDR region is selected from the group consisting of: S179P, one of E184K, E184G, or E184D, and S182F, or the light chain comprises or consists of a variable region according to amino acid sequence SEQ ID NO: 2 in which said at least one substitution in said CDR region is selected from the group consisting of: S179P, one of E184K, E184G, or E184D, and S182F, and said at least one substitution in the FR regions of VL is a substitution of at least one amino acid selected from the group consisting of: of I177T, I132T, A143T, T150A, S158P, L175Q, Y178H, V187A, S192T, G197D, or F212S, and a constant region according to amino acid sequence SEQ ID NO: 6, and
b) the heavy chain comprises or consists of a variable region according to amino acid sequence SEQ ID NO: 8 in which said at least one substitution is selected from the group consisting of: Q1E, Q3E or Q3R, Q6E, A9T, V11A, K12R, K13R, K19E, V20A, one of A24G, A24V or A24T, Q39E, A40V, S31G, L45P, D56N, A76T, A79T, R87G, T58A, Q62R, V67M, I70N, T74A, S77P, A79T, S88P, E89D, F102S, A103T, L110P, and 5114T.
6. The mutated humanized 12G4 monoclonal antibody according to claim 1 , wherein
a) the light chain comprises or consists of a variable region according to an amino acid sequence selected from the group consisting of: SEQ ID NO: 22 or SEQ ID NO: 24, SEQ ID NO: 30 or SEQ ID NO: 32, SEQ ID NO: 34 or SEQ ID NO: 36, and SEQ ID NO: 46 or SEQ ID NO: 48, and of a constant region according to amino acid sequence SEQ ID NO: 6, and
b) the heavy chain comprises or consists of a variable region according to an amino acid sequence selected from the group consisting of: SEQ ID NO: 38 or SEQ ID NO: 40, SEQ ID NO: 26 or SEQ ID NO: 28, SEQ ID NO: 8 or SEQ ID NO: 10, SEQ ID NO: 42 or SEQ ID NO: 44, and SEQ ID NO: 50 or SEQ ID NO: 52, and of a constant region according to amino acid sequence SEQ ID NO: 12.
7. The mutated humanized 12G4 monoclonal antibody according to claim 5 , wherein the combination of the light chain and the heavy chain is selected from the group consisting of:
a) the light chain consists of SEQ ID NO: 70 or SEQ ID NO: 72, and
b) the heavy chain consists of SEQ ID NO: 74 or SEQ ID NO: 76;
a) the light chain consists of SEQ ID NO: 78 or SEQ ID NO: 80, and
b) the heavy chain consists of SEQ ID NO: 58 or SEQ ID NO: 60;
a) the light chain consists of SEQ ID NO: 82 or SEQ ID NO: 84, and
b) the heavy chain consists of SEQ ID NO: 86 or SEQ ID NO: 88;
a) the light chain consists of SEQ ID NO: 78 or SEQ ID NO: 80, and
b) the heavy chain consists of SEQ ID NO: 90 or SEQ ID NO: 92; and
a) the light chain consists of SEQ ID NO: 94 or SEQ ID NO: 96, and
b) the heavy chain consists of SEQ ID NO: 98 or SEQ ID NO: 100.
8. A fragment of the mutated humanized 12G4 monoclonal antibody according to claim 1 , selected from the group consisting of: Fv, Fab, F(ab′)2, Fab′, dsFv, scFv, Sc(Fv) 2 , and diabodies.
9. Pharmaceutical composition, comprising at least
a monoclonal antibody according to claim 1 , or
a fragment of said monoclonal antibody selected from the group consisting of: Fv, Fab, F(ab′)2, Fab′, dsFv, scFv, Sc(Fv) 2 , and diabodies,
together with a pharmaceutically acceptable vehicle.
10. Product comprising a first pharmaceutical preparation comprising a monoclonal antibody according to claim 1 , and a second pharmaceutical preparation comprising a conventional anticancer compound as a combined preparation for simultaneous, separate or sequential use in the treatment of patients with ovarian cancers.
11. A kit comprising at least:
the mutated monoclonal antibody according to claim 1 , or
a fragment of said mutated monoclonal antibody selected from the group of fragments consisting of: Fv, Fab, F(ab′)2, Fab′, dsFv, scFv, Sc(Fv) 2 , and diabodies,
for use in diagnosing a pathology associated with the human anti-Müllerian hormone type II receptor.