Anti-human tenascin monoclonal antibody
View Patent ↗An anti-human tenascin monoclonal antibody is described, whose light and heavy chain variable region sequences are SEQ ID 1 and SEQ ID 2, respectively, its proteolytic fragments capable of binding to an antigenic epitope within the region A (1-4) -D of human tenascin, its recombinant derivatives, its conjugates and its similar functional analogues capable of binding to an antigenic epitope within the A (1-4) -D region of human tenascin.
1. An isolated anti-human tenascin monoclonal antibody or a proteolytic fragment thereof, comprising a light chain variable region of SEQ ID NO:2 and a heavy chain variable region of SEQ ID NO:4, wherein said light chain variable region and said heavy chain variable region are capable of binding to an antigenic epitope within the A (1-4) -D region of human tenascin.
2. The fragment of the antibody according to claim 1 , further containing additional markers and diagnostic agents.
3. The antibody or the fragment thereof according to claim 1 , wherein said antibody or said fragment thereof are biotinylated.
4. An isolated antibody or a fragment thereof coded for by the nucleotide sequences SEQ ID NO:1 and SEQ ID NO:3.
5. Hybridoma producing the antibody according to claim 1 , deposited at the Centro di Biotecnologie Avanzate, Largo Rossana Benzi 10 Genoa - Italy on 12 November 2003 in accordance with the provisions of the Budapest Treaty, with the accession number PD03003.
6. Process for the preparation of the antibody according to claim 1 comprising
a) immunizing an animal with the A (1-4) -D fragment of human tenascin;
b) fusing somatic spleen cells of said animal with myeloma cells not producing immunoglobulins;
c) selecting the monoclonal antibody.
7. A pharmaceutical or diagnostic composition containing an antibody or a proteolytic fragment thereof according to claim 1 , with at least one pharmaceutically acceptable vehicle or excipient.
8. A kit for systemic radioimmunotherapy consisting of 5 vials: wherein vial 1 contains the antibody or the proteolytic fragment thereof according to claim 1 ; vial 2 contains avidin; vial 3 contains streptavidin; vial 4 contains biotinylated human albumin; and vial 5 contains biotin DOTA.
9. A kit for locoregional radioimmunotherapy consisting of 3 vials; wherein vial 1 contains the antibody or the proteolytic fragment thereof according to claim 1 , vial 2 contains avidin; and vial 3 contains biotin DOTA.
10. The kit according to claim 8 wherein said biotin DOTA in vial 5 is the formula (I) compound
in which Q is a —(CH 2 )n-group, where n is a whole number from 4 to 12, in which case R′ is not present, or Q is selected from the group consisting of —(CH 2 ) a —CH(R′) b —(CH 2 ) b —, where a and b are independently whole numbers from 0 to n, wherein n is as defined above, R′ is as defined here below, or Q is cyclohexyl, phenyl, in which case R′ is a substituted on the cyclohexyl or phenyl ring;
R is hydrogen or -Λ where -Λ is a formula (II) macrocycle
where the various Y's which may be the same or different, are selected from the group consisting of hydrogen, straight or branched C 1 —C 4 alkyl, —(CH 2 ) m —COOH, where m is a whole number from 1 to 3, X is hydrogen, or the group —CH 2 —U, where U is selected from the group consisting or methyl, ethyl, and p-aminophenyl, or X is the group —(CHW) o —Z, where o is a whole number from 1 to 5, W is hydrogen, methyl or ethyl, Z is a 5- or 6- member heterocyclic group containing one or more heteroatoms selected from O, N—R 1 , where R 1 is hydrogen or straight or branched C 1 -C 4 alkyl, and S; or Z is selected from the group consisting of —NH 2 , —NH—C(═NH)—NH 2 , or —S—R 2 , where R 2 is straight or branched C 1 -C 4 alkyl;
p is the number 2 or 3;
R′ is selected from the group consisting of hydrogen, straight or branched C 1 -C 4 alkyl, —(CH 2 ) q -T, in which T is selected from the group consisting of —S—CH 3 , —OH, —COOH, and q is the number 1 or 2;
R″ has the same meanings as R′, upon the following conditions: if R is -Λ, R″ is hydrogen, if R is hydrogen, R″ is -Λ, or R and R″ are, respectively —(CH 2 ) r -Λ(for R), where r is a whole number from 4to 12, and -Λ(for R′), Q being a —(CH 2 ) n — group, where n is a whole number from 4 to 12.
11. The kit according to claim 8 , in which vial 3 contains an avidin dimer in which two avidin molecules are bound via the —NH 2 groups by means of suberate.
12. The kit according to claim 8 , in which said vial 3 contains an avidin dimer in which two avidin molecules are bound via the —COOH groups by means of polyethylene glycol with a molecular weight of 3,400.
13. The kit according to claim 8 , in which the antibody or the proteolytic fragment thereof are combined with other anti-tenascin antibodies.
14. The kit according to claim 8 , wherein the antibody or the proteolytic fragment thereof are combined with other tumor-specific antibodies.
15. Container containing the antibody or the proteolytic fragment thereof according to claim 1 .
16. Combination comprising the antibody or the proteolytic fragment thereof according to claim 1 , and a second tenascin-specific antibody.
17. An isolated murine anti-human tenascin monoclonal antibody or a proteolytic fragment thereof comprising a light chain variable region of SEQ ID NO:2 and a heavy chain variable region of SEQ ID NO:4, wherein said light chain variable region and said heavy chain variable region are capable of binding to an antigenic epitope within the A (1-4) -D region of human tenascin.
18. An antibody or a fragment thereof according to claim 17 comprising a human constant region.
19. The kit according to claim 9 wherein in which said biotin DOTA
in vial 2 is the formula (I) compound
in which Q is a —(CH 2 )n—group, where n is a whole number from 4 to 12, in which case R′ is not present, or Q is selected from the group consisting of —(CH 2 ) a —CH(R′) b —(CH 2 ) b —, where a and b are independently whole numbers from 0 to n, wherein n is as defined above, R′ is as defined here below, or Q is cyclohexyl, phenyl, in which case R′ is a substituted on the cyclohexyl or phenyl ring;
R is hydrogen or -Λ where -Λ is a formula (II) macrocycle
where the various Y's which may be the same or different, are selected from the group consisting of hydrogen, straight or branched C 1 -C 4 alkyl, —(CH 2 ) m —COOH, where m is a whole number from 1 to 3, X is hydrogen, or the group —CH 2 —U, where U is selected from the group consisting or methyl, ethyl, and p-aminophenyl, or X is the group —(CHW) o -Z, where o is a whole number from 1 to 5, W is hydrogen, methyl or ethyl, Z is a 5- or 6- member heterocyclic group containing one or more heteroatoms selected from O, N—R 1 , where R 1 is hydrogen or straight or branched C 1 -C 4 alkyl, and S; or Z is selected from the group consisting of —NH 2 , —NH—C(═NH)—NH 2 , or —S—R 2 , where R 2 is straight or branched C 1 -C 4 alkyl;
p is the number 2 or 3;
R′ is selected from the group consisting of hydrogen, straight or branched C 1 -C 4 alkyl, —(CH 2 ) q -T, in which T is selected from the group consisting of —S—CH 3 , —OH, —COOH, and q is the number 1 or 2;
R″ has the same meanings as R′, upon the following conditions: if R is -Λ, R″ is hydrogen, if R is hydrogen, R″ is -Λ, or R and R″ are, respectively —(CH 2 ) r -Λ(for R), where r is a whole number from 4 to 12, and -Λ(for R′), Q being a —(CH 2 ) n — group, where n is a whole number from 4 to 12.