Antibodies directed to the deletion mutants of epidermal growth factor receptor and uses thereof
The present invention relates to novel antibodies, particularly antibodies directed against deletion mutants of epidermal growth factor receptor and particularly to the type III deletion mutant, EGFRvIII. The invention also relates to human monoclonal antibodies directed against deletion mutants of epidermal growth factor receptor and particularly to EGFRvIII. Diagnostic and therapeutic formulations of such antibodies, and immunoconjugates thereof, are also provided.
1. A method of inhibiting cell proliferation associated with the expression of EGFRvIII that comprises the amino acid sequence of SEQ ID NO: 56, said method comprising treating cells expressing EGFRvIII with an effective amount of an antibody, wherein said antibody binds to LEEKKGNYVVTDHC (SEQ ID NO: 56) of EGFRvIII and wherein the antibody is
a) an antibody comprising a heavy chain variable region amino acid sequence of SEQ ID NO: 142 and a light chain variable region amino acid sequence of SEQ ID NO: 144,
b) an antibody comprising a heavy chain variable region amino acid sequence of SEQ ID NO: 2 and a light chain variable region amino acid sequence of SEQ ID NO: 19,
c) an antibody comprising a heavy chain variable region amino acid sequence of SEQ ID NO: 4 and a light chain variable region amino acid sequence of SEQ ID NO: 20,
d) an antibody comprising a heavy chain variable region amino acid sequence of SEQ ID NO: 5 and a light chain variable region amino acid sequence of SEQ ID NO: 21,
e) an antibody comprising a heavy chain variable region amino acid sequence of SEQ ID NO: 7 and a light chain variable region amino acid sequence of SEQ ID NO: 23,
f) an antibody comprising a heavy chain variable region amino acid sequence of SEQ ID NO: 9 and a light chain variable region amino acid sequence of SEQ ID NO: 26,
g) an antibody comprising a heavy chain variable region amino acid sequence of SEQ ID NO: 10 and a light chain variable region amino acid sequence of SEQ ID NO: 25,
h) an antibody comprising a heavy chain variable region amino acid sequence of SEQ ID NO: 12 and a light chain variable region amino acid sequence of SEQ ID NO: 28,
b) an antibody comprising a heavy chain variable region amino acid sequence of SEQ ID NO: 13 and a light chain variable region amino acid sequence of SEQ ID NO: 29,
j) an antibody comprising a heavy chain variable region amino acid sequence of SEQ ID NO: 15 and a light chain variable region amino acid sequence of SEQ ID NO: 33,
k) an antibody comprising a heavy chain variable region amino acid sequence of SEQ ID NO: 16 and a light chain variable region amino acid sequence of SEQ ID NO: 31, or
l) an antibody comprising a heavy chain variable region amino acid sequence of SEQ ID NO: 17 and a light chain variable region amino acid sequence of SEQ ID NO: 32.
2. The method of claim 1 , wherein the method is performed in vivo.
3. The method of claim 1 , wherein the method is performed on mammal.
4. The method of claim 3 , wherein the mammal is a human.
5. The method of claim 3 , wherein the mammal suffers from a cancer involving epithelial cell proliferation associated with the expression of EGFRvIII.
6. The method of claim 5 , wherein the cancer comprises a lung, colon, gastric, renal, prostate, breast, glioblastoma or ovarian carcinoma.
7. A method of inhibiting cell proliferation associated with the expression of EGFRvIII, that comprises the amino acid sequence of SEQ ID NO: 56, said method comprising treating cells expressing EGFRvIII with an effective amount of an isolated antibody that binds to LEEKKGNYVVTDHC (SEQ ID NO: 56) of EGFRvIII, wherein the antibody is
(a) an antibody comprising a heavy chain polypeptide comprising the following complementarity determining regions (CDRs): a heavy chain CDR1 that is a CDR1 in SEQ ID NO: 142; a heavy chain CDR2 that is a CDR2 in SEQ ID NO: 142; a heavy chain CDR3 that is a CDR3 in SEQ ID NO: 142; and a light chain polypeptide comprising the following CDRs: a light chain CDR1that is a CDR1 in SEQ ID NO: 144; a light chain CDR2 that is a CDR2 in SEQ ID NO: 144; and a light chain CDR3 that is a CDR3 in SEQ ID NO: 144,
(b) an antibody comprising a heavy chain polypeptide comprising the following complementarity determining regions (CDRs): a heavy chain CDR1 that is a CDR1 in SEQ ID NO: 2; a heavy chain CDR2 that is a CDR2 in SEQ ID NO: 2; a heavy chain CDR3 that is a CDR3 in SEQ ID NO: 2; and a light chain polypeptide comprising the following CDRs: a light chain CDR1 that is a CDR1 in SEQ ID NO: 19; a light chain CDR2 that is a CDR2 in SEQ ID NO: 19; and a light chain CDR3 that is a CDR3 in SEQ ID NO: 19,
(c) an antibody comprising a heavy chain polypeptide comprising the following complementarity determining regions (CDRs): a heavy chain CDR1 that is a CDR1 in SEQ ID NO: 4; a heavy chain CDR2 that is a CDR2 in SEQ ID NO: 4; a heavy chain CDR3 that is a CDR3 in SEQ ID NO: 4; and a light chain polypeptide comprising the following CDRs: a light chain CDR1that is a CDR1 in SEQ ID NO: 20; a light chain CDR2 that is a CDR2 in SEQ ID NO: 20; and a light chain CDR3 that is a CDR3 in SEQ ID NO: 20,
(d) an antibody comprising a heavy chain polypeptide comprising the following complementarity determining regions (CDRs): a heavy chain CDR1 that is a CDR1 in SEQ ID NO: 5; a heavy chain CDR2 that is a CDR2 in SEQ ID NO: 5; a heavy chain CDR3 that is a CDR3 in SEQ ID NO: 5; and a light chain polypeptide comprising the following CDRs: a light chain CDR1that is a CDR1 in SEQ ID NO: 21; a light chain CDR2 that is a CDR2 in SEQ ID NO: 21; and a light chain CDR3 that is a CDR3 in SEQ ID NO: 21,
(e) an antibody comprising a heavy chain polypeptide comprising the following complementarity determining regions (CDRs): a heavy chain CDR1 that is a CDR1 in SEQ ID NO: 7; a heavy chain CDR2 that is a CDR2 in SEQ ID NO: 7; a heavy chain CDR3 that is a CDR3 in SEQ ID NO: 7; and a light chain polypeptide comprising the following CDRs: a light chain CDR1that is a CDR1 in SEQ ID NO: 23; a light chain CDR2 that is a CDR2 in SEQ ID NO: 23; and a light chain CDR3 that is a CDR3 in SEQ ID NO: 23,
(f) an antibody comprising a heavy chain polypeptide comprising the following complementarity determining regions (CDRs): a heavy chain CDR1 that is a CDR1 in SEQ ID NO: 9; a heavy chain CDR2 that is a CDR2 in SEQ ID NO: 9; a heavy chain CDR3 that is a CDR3 in SEQ ID NO: 9; and a light chain polypeptide comprising the following CDRs: a light chain CDR1that is a CDR1 in SEQ ID NO: 26; a light chain CDR2 that is a CDR2 in SEQ ID NO: 26; and a light chain CDR3 that is a CDR3 in SEQ ID NO: 26,
(g) an antibody comprising a heavy chain polypeptide comprising the following complementarity determining regions (CDRs): a heavy chain CDR1 that is a CDR1 in SEQ ID NO: 10; a heavy chain CDR2 that is a CDR2 in SEQ ID NO: 10; a heavy chain CDR3 that is a CDR3 in SEQ ID NO: 25; and a light chain polypeptide comprising the following CDRs: a light chain CDR1that is a CDR1 in SEQ ID NO: 25; a light chain CDR2 that is a CDR2 in SEQ ID NO: 25; and a light chain CDR3 that is a CDR3 in SEQ ID NO: 25,
(h) an antibody comprising a heavy chain polypeptide comprising the following complementarity determining regions (CDRs): a heavy chain CDR1 that is a CDR1 in SEQ ID NO: 12; a heavy chain CDR2 that is a CDR2 in SEQ ID NO: 12; a heavy chain CDR3 that is a CDR3 in SEQ ID NO: 12; and a light chain polypeptide comprising the following CDRs: a light chain CDR1that is a CDR1 in SEQ ID NO: 28; a light chain CDR2 that is a CDR2 in SEQ ID NO: 28; and a light chain CDR3 that is a CDR3 in SEQ ID NO: 28,
(i) an antibody comprising a heavy chain polypeptide comprising the following complementarity determining regions (CDRs): a heavy chain CDR1 that is a CDR1 in SEQ ID NO: 13; a heavy chain CDR2 that is a CDR2 in SEQ ID NO: 13; a heavy chain CDR3 that is a CDR3 in SEQ ID NO: 13; and a light chain polypeptide comprising the following CDRs: a light chain CDR1that is a CDR1 in SEQ ID NO: 29; a light chain CDR2 that is a CDR2 in SEQ ID NO: 29; and a light chain CDR3 that is a CDR3 in SEQ ID NO: 29,
(j) an antibody comprising a heavy chain polypeptide comprising the following complementarity determining regions (CDRs): a heavy chain CDR1 that is a CDR1 in SEQ ID NO: 15; a heavy chain CDR2 that is a CDR2 in SEQ ID NO: 15; a heavy chain CDR3 that is a CDR3 in SEQ ID NO: 15; and a light chain polypeptide comprising the following CDRs: a light chain CDR1that is a CDR1 in SEQ ID NO: 33; a light chain CDR2 that is a CDR2 in SEQ ID NO: 33; and a light chain CDR3 that is a CDR3 in SEQ ID NO: 33,
(k) an antibody comprising a heavy chain polypeptide comprising the following complementarity determining regions (CDRs): a heavy chain CDR1 that is a CDR1 in SEQ ID NO: 16; a heavy chain CDR2 that is a CDR2 in SEQ ID NO: 16; a heavy chain CDR3 that is a CDR3 in SEQ ID NO: 16; and a light chain polypeptide comprising the following CDRs: a light chain CDR1that is a CDR1 in SEQ ID NO: 31; a light chain CDR2 that is a CDR2 in SEQ ID NO: 31; and a light chain CDR3 that is a CDR3 in SEQ ID NO: 31,
(l) an antibody comprising a heavy chain polypeptide comprising the following complementarity determining regions (CDRs): a heavy chain CDR1 that is a CDR1 in SEQ ID NO: 17; a heavy chain CDR2 that is a CDR2 in SEQ ID NO: 17; a heavy chain CDR3 that is a CDR3 in SEQ ID NO: 17; and a light chain polypeptide comprising the following CDRs: a light chain CDR1that is a CDR1 in SEQ ID NO: 32; a light chain CDR2 that is a CDR2 in SEQ ID NO: 32; and a light chain CDR3 that is a CDR3 in SEQ ID NO: 32.
8. The method of claim 7 , wherein the method is performed in vivo.
9. The method of claim 7 , wherein the method is performed on mammal.
10. The method of claim 9 , wherein the mammal is a human.
11. The method of claim 9 , wherein the mammal suffers from a cancer involving epithelial cell proliferation associated with the expression of EGFRvIII.
12. The method of claim 11 , wherein the cancer comprises a lung, colon, gastric, renal, prostate, breast, glioblastoma or ovarian carcinoma.
13. A method of inhibiting cell proliferation associated with the expression of EGFRvIII that comprises the amino acid sequence of SEQ ID NO: 56, said method comprising treating cells expressing EGFRvIII with an effective amount of an isolated antibody that binds to EGFRvIII, wherein the antibody is
a) an antibody comprising a heavy chain polypeptide comprising the following complementarity determining regions (CDRs): a heavy chain CDR1 that is a CDR1 in SEQ ID NO: 142; a heavy chain CDR2 that is a CDR2 in SEQ ID NO: 142; a heavy chain CDR3 that is a CDR3 in SEQ ID NO: 142; and a light polypeptide comprising the following CDRs: a light chain CDR1 that is a CDR1 in SEQ ID NO: 144; a light chain CDR2 that is a CDR2 in SEQ ID NO: 144; and a light chain CDR3 that is a CDR3 in SEQ ID NO: 144,
b) an antibody comprising a heavy chain polypeptide comprising the following complementarity determining regions (CDRs): a heavy chain CDR1 that is a CDR1 in SEQ ID NO: 2; a heavy chain CDR2 that is a CDR2 in SEQ ID NO: 2; a heavy chain CDR3 that is a CDR3 in SEQ ID NO: 2; and a light polypeptide comprising the following CDRs: a light chain CDR1 that is a CDR1 in SEQ ID NO: 19; a light chain CDR2 that is a CDR2 in SEQ ID NO: 19; and a light chain CDR3 that is a CDR3 in SEQ ID NO: 19,
c) an antibody comprising a heavy chain polypeptide comprising the following complementarity determining regions (CDRs): a heavy chain CDR1 that is a CDR1 in SEQ ID NO: 4; a heavy chain CDR2 that is a CDR2 in SEQ ID NO: 4; a heavy chain CDR3 that is a CDR3 in SEQ ID NO: 4; and a light polypeptide comprising the following CDRs: a light chain CDR1 that is a CDR1 in SEQ ID NO: 20; a light chain CDR2 that is a CDR2 in SEQ ID NO: 20; and a light chain CDR3 that is a CDR3 in SEQ ID NO: 20,
d) an antibody comprising a heavy chain polypeptide comprising the following complementarity determining regions (CDRs): a heavy chain CDR1 that is a CDR1 in SEQ ID NO: 5; a heavy chain CDR2 that is a CDR2 in SEQ ID NO: 5; a heavy chain CDR3 that is a CDR3 in SEQ ID NO: 5; and a light polypeptide comprising the following CDRs: a light chain CDR1 that is a CDR1 in SEQ ID NO: 21; a light chain CDR2 that is a CDR2 in SEQ ID NO: 21; and a light chain CDR3 that is a CDR3 in SEQ ID NO: 21,
e) an antibody comprising a heavy chain polypeptide comprising the following complementarity determining regions (CDRs): a heavy chain CDR1 that is a CDR1 in SEQ ID NO: 7; a heavy chain CDR2 that is a CDR2 in SEQ ID NO: 7; a heavy chain CDR3 that is a CDR3 in SEQ ID NO: 7; and a light polypeptide comprising the following CDRs: a light chain CDR1 that is a CDR1 in SEQ ID NO: 23; a light chain CDR2 that is a CDR2 in SEQ ID NO: 23; and a light chain CDR3 that is a CDR3 in SEQ ID NO: 23,
f) an antibody comprising a heavy chain polypeptide comprising the following complementarity determining regions (CDRs): a heavy chain CDR1 that is a CDR1 in SEQ ID NO: 9; a heavy chain CDR2 that is a CDR2 in SEQ ID NO: 9; a heavy chain CDR3 that is a CDR3 in SEQ ID NO: 9; and a light polypeptide comprising the following CDRs: a light chain CDR1 that is a CDR1 in SEQ ID NO: 26; a light chain CDR2 that is a CDR2 in SEQ ID NO: 26; and a light chain CDR3 that is a CDR3 in SEQ ID NO: 26,
g) an antibody comprising a heavy chain polypeptide comprising the following complementarity determining regions (CDRs): a heavy chain CDR1 that is a CDR1 in SEQ ID NO: 10; a heavy chain CDR2 that is a CDR2 in SEQ ID NO: 10; a heavy chain CDR3 that is a CDR3 in SEQ ID NO: 10; and a light polypeptide comprising the following CDRs: a light chain CDR1 that is a CDR1 in SEQ ID NO: 25; a light chain CDR2 that is a CDR2 in SEQ ID NO: 25; and a light chain CDR3 that is a CDR3 in SEQ ID NO: 25,
h) an antibody comprising a heavy chain polypeptide comprising the following complementarity determining regions (CDRs): a heavy chain CDR1 that is a CDR1 in SEQ ID NO: 12; a heavy chain CDR2 that is a CDR2 in SEQ ID NO: 12; a heavy chain CDR3 that is a CDR3 in SEQ ID NO: 12; and a light polypeptide comprising the following CDRs: a light chain CDR1 that is a CDR1 in SEQ ID NO: 28; a light chain CDR2 that is a CDR2 in SEQ ID NO: 28; and a light chain CDR3 that is a CDR3 in SEQ ID NO: 28,
i) an antibody comprising a heavy chain polypeptide comprising the following complementarity determining regions (CDRs): a heavy chain CDR1 that is a CDR1 in SEQ ID NO: 13; a heavy chain CDR2 that is a CDR2 in SEQ ID NO: 13; a heavy chain CDR3 that is a CDR3 in SEQ ID NO: 13; and a light polypeptide comprising the following CDRs: a light chain CDR1 that is a CDR1 in SEQ ID NO: 29; a light chain CDR2 that is a CDR2 in SEQ ID NO: 29; and a light chain CDR3 that is a CDR3 in SEQ ID NO: 29,
j) an antibody comprising a heavy chain polypeptide comprising the following complementarity determining regions (CDRs): a heavy chain CDR1 that is a CDR1 in SEQ ID NO: 15; a heavy chain CDR2 that is a CDR2 in SEQ ID NO: 15; a heavy chain CDR3 that is a CDR3 in SEQ ID NO: 15; and a light polypeptide comprising the following CDRs: a light chain CDR1 that is a CDR1 in SEQ ID NO: 33; a light chain CDR2 that is a CDR2 in SEQ ID NO: 33; and a light chain CDR3 that is a CDR3 in SEQ ID NO: 33,
k) an antibody comprising a heavy chain polypeptide comprising the following complementarity determining regions (CDRs): a heavy chain CDR1 that is a CDR1 in SEQ ID NO: 16; a heavy chain CDR2 that is a CDR2 in SEQ ID NO: 16; a heavy chain CDR3 that is a CDR3 in SEQ ID NO: 16; and a light polypeptide comprising the following CDRs: a light chain CDR1 that is a CDR1 in SEQ ID NO: 31; a light chain CDR2 that is a CDR2 in SEQ ID NO: 31; and a light chain CDR3 that is a CDR3 in SEQ ID NO: 31,
l) an antibody comprising a heavy chain polypeptide comprising the following complementarity determining regions (CDRs): a heavy chain CDR1 that is a CDR1 in SEQ ID NO: 17; a heavy chain CDR2 that is a CDR2 in SEQ ID NO: 17; a heavy chain CDR3 that is a CDR3 in SEQ ID NO: 17; and a light polypeptide comprising the following CDRs: a light chain CDR1 that is a CDR1 in SEQ ID NO: 32; a light chain CDR2 that is a CDR2 in SEQ ID NO: 32; and a light chain CDR3 that is a CDR3 in SEQ ID NO: 32,
wherein each CDR is defined in accordance with the CDR definition of Kabat or Chothia.
14. The method of claim 13 , wherein each CDR is defined in accordance with the CDR definition of Kabat.
15. The method of claim 13 , wherein each CDR is defined in accordance with the CDR definition of Chothia.
16. The method of claim 13 , wherein the antibody comprises a heavy chain polypeptide comprising the following complementarity determining regions (CDRs): a heavy chain CDR1 that is a CDR1 in SEQ ID NO: 2; a heavy chain CDR2 that is a CDR2 in SEQ ID NO: 2; a heavy chain CDR3 that is a CDR3 in SEQ ID NO: 2; and a light chain polypeptide comprising the following CDRs: a light chain CDR1 that is a CDR1 in SEQ ID NO: 19; a light chain CDR2 that is a CDR2 in SEQ ID NO: 19; and a light chain CDR3 that is a CDR3 in SEQ ID NO: 19.
17. The method of claim 16 , wherein the method is performed in vivo.
18. The method of claim 16 , wherein the method is performed on mammal.
19. The method of claim 16 , wherein the mammal is a human.
20. The method of claim 16 , wherein the mammal suffers from a cancer involving epithelial cell proliferation associated with the expression of EGFRvIII.
21. The method of claim 16 , wherein the cancer comprises a lung, colon, gastric, renal, prostate, breast, glioblastoma or ovarian carcinoma.
22. A method of inhibiting cell proliferation associated with the expression of EGFRvIII that comprises the amino acid sequence of SEQ ID NO: 56, said method, comprising treating cells expressing EGFRvIII with an effective amount of an isolated antibody that binds to LEEKKGNYVVTDHC (SEQ ID NO: 56) of EGFRvIII and wherein the antibody comprises:
a heavy chain polypeptide, wherein CDR3 of the heavy chain polypeptide comprises the amino acid sequence in SEQ ID NO: 112, wherein CDR2 of the heavy chain polypeptide comprises the amino acid sequence in SEQ ID NO: 110, and wherein CDR1 of the heavy chain polypeptide comprises the amino acid sequence in SEQ ID NO: 108; and
a light chain polypeptide, wherein CDR3 of the heavy chain polypeptide comprises the amino acid sequence in SEQ ID NO: 105, wherein CDR2 of the light chain polypeptide comprises the amino acid sequence in SEQ ID NO: 103, and wherein CDR1 of the light chain polypeptide comprises the amino acid sequence in SEQ ID NO: 101.
23. The method of claim 1 , wherein the antibody comprises a heavy chain variable region amino acid sequence of SEQ ID NO: 2 and a light chain variable region amino acid sequence of SEQ ID NO: 19.
24. The method of claim 7 , wherein the antibody comprises a heavy chain polypeptide comprising the following complementarity determining regions (CDRs): a heavy chain CDR1 that is a CDR1 in SEQ ID NO: 2; a heavy chain CDR2 that is a CDR2 in SEQ ID NO: 2; a heavy chain CDR3 that is a CDR3 in SEQ ID NO: 2; and a light chain polypeptide comprising the following CDRs: a light chain CDR1 that is a CDR1 in SEQ ID NO: 19; a light chain CDR2 that is a CDR2 in SEQ ID NO: 19; and a light chain CDR3 that is a CDR3 in SEQ ID NO: 19.
25. The method of claim 1 , wherein the antibody comprises a heavy chain variable region amino acid sequence of SEQ ID NO: 142 and a light chain variable region amino acid sequence of SEQ ID NO: 144.
26. The method of claim 7 , wherein the antibody comprises a heavy chain polypeptide comprising the following complementarity determining regions (CDRs): a heavy chain CDR1 that is a CDR1 in SEQ ID NO: 142; a heavy chain CDR2 that is a CDR2 in SEQ ID NO: 142; a heavy chain CDR3 that is a CDR3 in SEQ ID NO: 142; and a light chain polypeptide comprising the following CDRs: a light chain CDR1 that is a CDR1 in SEQ ID NO: 144; a light chain CDR2 that is a CDR2 in SEQ ID NO: 144; and a light chain CDR3 that is a CDR3 in SEQ ID NO: 144.