Antibodies which bind to epithelial membrane protein 2 (EMP2)
The present invention provides methods and compositions useful in the treatment or prevention of Chlamydia infections and cancer. The methods and compositions inhibit the entry of Chlamydia into a host cell expressing EMP2 by interfering with the interaction between the Chlamydia and EMP2. The methods and compositions target cancers which express or overexpress EMP2 nucleic acids and polypeptides by targeting EMP2.
1. An isolated antibody that competes for binding to the extracellular loop of human Epithelial Membrane Protein 2 (EMP2) (SEQ ID NO: 42) with an EMP2 inhibitor, wherein the antibody comprises a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region comprises three heavy chain complementary determining regions (HCDRs) and wherein the light chain variable region comprises three light chain variable regions (LCDRs), wherein:
the sequence of HCDR1 is EYPMH (SEQ ID NO: 15),
the sequence of HCDR2 is VISYDGEYQKYADSVKG (SEQ
ID NO: 17),
the sequence of HCDR3 is TINNGMDV (SEQ ID NO: 41),
the sequence of LCDR1 is RASQGIRNDLG (SEQ ID NO:
20),
the sequence of LCDR2 is GASSLQS (SEQ ID NO: 23),
and
the sequence of LCDR3 is LQDYNGWT (SEQ ID NO: 40).
2. The antibody of claim 1 , wherein the antibody is a monoclonal antibody, a humanized monoclonal antibody, a human antibody, a diabody, minibody, or triabody, a chimeric antibody, or a recombinant antibody.
3. The antibody of claim 1 , wherein the antibody is in an scFv, minibody, diabody, or triabody format.
4. The antibody of claim 1 , wherein the antibody is conjugated to a cytotoxic agent or a label.
5. A pharmaceutical composition comprising the antibody of claim 1 and a physiologically acceptable carrier.
6. An isolated antibody which binds to Epithelial Membrane Protein 2 (EMP2), wherein the antibody comprises a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region comprises three heavy chain complementary determining regions (HCDRs) and wherein the light chain variable region comprises three light chain complementary determining regions (LCDRs), wherein:
the sequence of HCDR1 is EYPMH (SEQ ID NO: 15),
the sequence of HCDR2 is VISYDGEYQKYADSVKG (SEQ
ID NO: 17),
the sequence of HCDR3 is TINNGMDV (SEQ ID NO: 41),
the sequence of LCDR1 is RASQGIRNDLG (SEQ ID NO:
20),
the sequence of LCDR2 is GASSLQS (SEQ ID NO: 23),
and
the sequence of LCDR3 is LQDYNGWT (SEQ ID NO: 40).
7. The antibody of claim 6 , wherein the antibody is a monoclonal antibody, a humanized monoclonal antibody, a human antibody, a diabody, minibody, or triabody, a chimeric antibody, or a recombinant antibody.
8. The antibody of claim 6 , wherein the antibody is in an scFv, minibody, diabody, or triabody format.
9. The antibody of claim 6 , wherein the antibody is conjugated to a cytotoxic agent or a label.
10. A pharmaceutical composition comprising the antibody of claim 6 and a physiologically acceptable carrier.