Anti-CD43 antibody and use thereof for cancer treatment
Provided is an antibody for treating a cancer, more specifically, an anti-CD43 antibody binding to an extracellular domain of CD43, compositions for treating a cancer or inhibiting a cancer stem cell comprising the antibody as an active ingredient, and methods for screening an agent of inhibiting a cancer stem cell.
1. A method of treating a cancer or inhibiting a cancer stem cell, comprising administering a pharmaceutically effective amount of an anti-CD43 antibody or an antigen-binding fragment thereof to a subject in need of treating the cancer or inhibiting a cancer stem cell, wherein the anti-CD43 antibody or the antigen-binding fragment thereof comprises:
a CDR1H of SEQ ID NO: 111,
a CDR2H of SEQ ID NO: 114,
a CDR3H of SEQ ID NO: 118,
a CDR1L of SEQ ID NO: 119,
a CDR2L of SEQ ID NO: 122, 123, or 124, and
a CDR3L of SEQ ID NO: 125.
2. The method of claim 1 , wherein the anti-CD43 antibody or an antigen-binding fragment thereof comprises:
a CDR1H of SEQ ID NO: 111,
a CDR2H of SEQ ID NO: 114,
a CDR3H of SEQ ID NO: 118,
a CDR1L of SEQ ID NO: 119,
a CDR2L of SEQ ID NO: 124, and
a CDR3L of SEQ ID NO: 125.
3. The method of claim 1 , wherein the cancer is a hematopoietic malignancy.
4. The method of claim 3 , wherein the hematopoietic malignancy is acute myeloid leukemia, acute lymphoblastic leukemia, acute monocytic leukemia, Hodgkin's lymphoma, or non-Hodgkin's lymphoma.
5. The method of claim 1 , wherein the cancer is a solid cancer.
6. The method of claim 5 , wherein the solid cancer is gastric cancer, breast cancer, lung cancer, colon cancer, liver cancer, gallbladder cancer, renal cancer, pancreatic cancer, thyroid cancer, prostatic cancer, ovarian cancer, cervical cancer, or bladder cancer.
7. The method of claim 1 , wherein the cancer stem cell is a cancer stem cell in hematopoietic malignancy or solid cancer.
8. The method of claim 1 , wherein the anti-CD43 antibody or the antigen-binding fragment thereof is administered together with a cytotoxic material.
9. The method of claim 8 , wherein the cytotoxic material is at least one selected from the group consisting of ricin, saporin, gelonin, momordin, debouganin, diphtheria toxin, pseudomonas toxin, radioisotopes, duocarmycin, monomethyl auristatin E (MMAE), monomethyl auristatin F (MMAF), N2′-deacetyl-N2′-(3-mercapto-1-oxopropyl)maytansine (DM1), and pyrrolobenzodiazepine (PBD) dimer.