Anti-Siglec-9 antibodies and methods of use thereof
The present disclosure is generally directed to compositions that include antibodies, e.g., monoclonal, chimeric, humanized antibodies, antibody fragments, etc., that specifically bind one or more epitopes within a Siglec-9 protein, e.g., human Siglec-9 or a mammalian Siglec-9, and use of such compositions in preventing, reducing risk, or treating an individual in need thereof.
1. A method of detecting Siglec-9 in a sample, comprising contacting the sample with an anti-Siglec-9 antibody, and detecting antibody-bound Siglec-9 in the sample, wherein the antibody comprises a light chain variable domain comprising an HVR-L1 comprising the amino acid sequence of SEQ ID NO: 6, an HVR-L2 comprising the amino acid sequence of SEQ ID NO: 10, an HVR-L3 comprising the amino acid sequence of SEQ ID NO: 14, and a heavy chain variable domain comprising an HVR-H1 comprising the amino acid sequence of SEQ ID NO: 19, an HVR-H2 comprising the amino acid sequence of SEQ ID NO: 22, and an HVR-H3 comprising the amino acid sequence of SEQ ID NO: 26.
2. The method of claim 1 , wherein the antibody comprises:
(a) a light chain variable domain comprising a VL FR1 comprising the amino acid sequence of SEQ ID NO: 30, an HVR-L1 comprising the amino acid sequence of SEQ ID NO: 6, a VL FR2 comprising the amino acid sequence of SEQ ID NO: 35, an HVR-L2 comprising the amino acid sequence of SEQ ID NO: 10, a VL FR3 comprising the amino acid sequence of SEQ ID NO: 39, an HVR-L3 comprising the amino acid sequence of SEQ ID NO: 14, and a VL FR4 comprising the amino acid sequence of SEQ ID NO: 44; and a heavy chain variable domain comprising a VH FR1 comprising the amino acid sequence of SEQ ID NO: 47, an HVR-H1 comprising the amino acid sequence of SEQ ID NO: 19, a VH FR2 comprising the amino acid sequence of SEQ ID NO: 51, an HVR-H2 comprising the amino acid sequence of SEQ ID NO: 22, a VH FR3 comprising the amino acid sequence of SEQ ID NO: 54, an HVR-H3 comprising the amino acid sequence of SEQ ID NO: 26, and a VH FR4 comprising the amino acid sequence of SEQ ID NO: 58; or
(b) a light chain variable domain comprising the amino acid sequence of SEQ ID NO: 61 and a heavy chain variable domain comprising the amino acid sequence of SEQ ID NO: 116.
3. The method of claim 1 , wherein the antibody is a murine IgG1, IgG2A, or IgG2B antibody.
4. The method of claim 1 , wherein the antibody-bound Siglec-9 is detected by immunohistochemistry, immunofluorescence microscopy, immunocytochemistry, ELISA, FACS analysis, immunoprecipitation, or micropositron emission tomography.
5. The method of claim 1 , wherein the sample is a biopsy specimen.
6. The method of claim 1 , comprising detecting antibody-bound Siglec-9 on primary cells selected from dendritic cells, bone marrow-derived dendritic cells, monocytes, microglia, macrophages, neutrophils, and NK cells, osteoclasts, T cells, T helper cells, cytotoxic T cells, or granulocytes.
7. The method of claim 1 , Wherein the sample is obtained from a subject suffering from cancer.
8. The method of claim 7 , wherein the cancer is selected from bladder cancer, brain cancer, breast cancer, colon cancer, rectal cancer, endometrial cancer, kidney cancer, renal cell cancer, renal pelvis cancer, leukemia, lung cancer, melanoma, non-Hodgkin's lymphoma, pancreatic cancer, prostate cancer, ovarian cancer, fibrosarcoma, acute lymphoblastic leukemia (ALL), acute myeloid leukemia (AML), chronic lymphocytic leukemia (CLL), chronic myeloid leukemia (CML), and multiple myeloma.
9. The method of claim 1 , wherein the sample is a human sample.
10. A method of detecting Siglec-9 in a sample, comprising contacting the sample with an anti-Siglec-9 antibody, and detecting antibody-bound Siglec-9 in the sample, wherein the antibody comprises a VL comprising the amino acid sequence of SEQ ID NO: 61 and a VH comprising the amino acid sequence of SEQ ID NO: 116.
11. The method of claim 10 , wherein the antibody is a murine IgG1, IgG2A, or IgG2B antibody.
12. The method of claim 10 , wherein the antibody-bound Siglec-9 is detected by immunohistochemistry, immunofluorescence microscopy, immunocytochemistry, ELISA, FACS analysis, immunoprecipitation, or micropositron emission tomography.
13. The method of claim 10 , comprising detecting antibody-bound Siglec-9 on primary cells selected from dendritic cells, bone marrow-derived dendritic cells, monocytes, microglia, macrophages, neutrophils, and NK cells, osteoclasts, T cells, T helper cells, cytotoxic T cells, or granulocytes.
14. The method of claim 10 , wherein the sample is obtained from a subject suffering from cancer.
15. The method of claim 14 , wherein the cancer is selected from bladder cancer, brain cancer, breast cancer, colon cancer, rectal cancer, endometrial cancer, kidney cancer, renal cell cancer, renal pelvis cancer, leukemia, lung cancer, melanoma, non-Hodgkin's lymphoma, pancreatic cancer, prostate cancer, ovarian cancer, fibrosarcoma, acute lymphoblastic leukemia (ALL), acute myeloid leukemia (AML), chronic lymphocytic leukemia (CLL), chronic myeloid leukemia (CML), and multiple myeloma.
16. The method of claim 10 , wherein the sample is a human sample.