Human monoclonal antibodies to Fucosyl-GM1 and methods for using anti-Fucosyl-GM1 antibodies
View Patent ↗The present disclosure provides isolated monoclonal antibodies, particularly human monoclonal antibodies that specifically bind to Fucosyl-GM1 with high affinity. Nucleic acid molecules encoding the antibodies of this disclosure, expression vectors, host cells and methods for expressing the antibodies of this disclosure are also provided. Immunoconjugates, bispecific molecules and pharmaceutical compositions comprising the antibodies of this disclosure are also provided. This disclosure also provides methods for detecting Fucosyl-GM1, as well as methods for treating various diseases, including cancer, using anti-Fucosyl-GM1 antibodies.
1. A method of treating a disease characterized by growth of tumor cells expressing Fucosyl-GM1, comprising administering to a subject a human monoclonal antibody that specifically binds to Fucosyl-GM1, or antigen-binding portion thereof, in an amount effective to treat the disease, wherein the human monoclonal antibody or antigen binding portion thereof cross-competes for binding to Fucosyl-GM1 with an antibody comprising:
(a) a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 4; and
(b) a light chain variable region comprising the amino acid sequence of SEQ ID NO: 10.
2. The method of claim 1 , wherein the disease is cancer.
3. The method of claim 2 , wherein the cancer is lung cancer.
4. The method of claim 3 , wherein the lung cancer is small cell lung cancer.
5. The method of claim 3 , wherein the lung cancer is non-small cell lung cancer.
6. The method of claim 1 , wherein the subject is human.
7. The method of claim 1 , wherein the antibody, or antigen-binding portion thereof, comprises:
(a) a heavy chain variable region CDR1 domain comprising SEQ ID NO:16;
(b) a heavy chain variable region CDR2 domain comprising SEQ ID NO:22;
(c) a heavy chain variable region CDR3 domain comprising SEQ ID NO:28;
(d) a light chain variable region CDR1 domain comprising SEQ ID NO:34;
(e) a light chain variable region CDR2 domain comprising SEQ ID NO:40; and
(f) a light chain variable region CDR3 domain comprising SEQ ID NO:46.
8. The method of claim 7 , wherein the antibody, or antigen-binding portion thereof, comprises:
(a) a heavy chain variable region comprising the amino acid sequence of SEQ ID NO:4; and
(b) a light chain variable region comprising the amino acid sequence of SEQ ID NO:10.
9. The method of claim 1 , wherein the antibody is a human antibody.
10. The method of claim 1 , wherein the antibody is a chimeric antibody or a humanized antibody.
11. The method of claim 1 , wherein the antibody is a full-length antibody of an IgG1 isotype or an IgG4 isotype.
12. The method of claim 1 , wherein the antibody is nonfucosylated.
13. The method of claim 1 , wherein the antibody or antigen-binding portion thereof, is linked to a therapeutic agent.
14. The method of claim 13 , wherein the therapeutic agent is a cytotoxin or a radioactive agent.
15. The method of claim 1 , wherein the antibody is administered by a route selected from subcutaneously, intravenously, intramuscularly, intradermally, and intraperitoneally.
16. The method of claim 1 , further comprising administering to the subject a second anti-neoplastic agent.