Isoform-selective TGFB1 inhibitors and use thereof
Disclosed herein are monoclonal antibodies and antigen-binding fragments thereof capable of selectively inhibiting TGFβ1 with high potency. Related compositions, methods and therapeutic use are also disclosed.
1. A method of treating a cancer in a subject, the method comprising a step of administering to the subject an antibody, or an antigen-binding fragment thereof, that binds pro-transforming growth factor beta 1 (proTGFβ1), wherein the antibody comprises:
a heavy chain complementary determining region 1 (H-CDR1) having an amino acid sequence set forth in SEQ ID NO: 107;
a heavy chain complementary determining region 2 (H-CDR2) having an amino acid sequence set forth in SEQ ID NO: 103;
a heavy chain complementary determining region 3 (H-CDR3) having an amino acid sequence set forth in SEQ ID NO: 6;
a light chain complementary determining region 1 (L-CDR1) having an amino acid sequence set forth in SEQ ID NO: 105;
a light chain complementary determining region 2 (L-CDR2) having an amino acid sequence set forth in SEQ ID NO: 106; and,
a light chain complementary determining region 3 (L-CDR3) having an amino acid sequence set forth in SEQ ID NO: 12,
thereby treating the cancer in the subject.
2. The method of claim 1 , wherein the subject previously received checkpoint blockade therapy (CBT) and was poorly responsive to the CBT.
3. The method of claim 1 , wherein the cancer is a type of cancer with statistically low response rates to CBT characterized by a response rate of under 25%.
4. The method of claim 1 , wherein the subject has not previously received CBT.
5. The method of claim 1 , wherein the cancer has primary resistance to checkpoint blockade therapy (CBT), and wherein the antibody, or antigen-binding fragment thereof, is administered to the subject in conjunction with a checkpoint inhibitor.
6. The method of claim 5 , wherein the antibody, or the antigen-binding fragment thereof, and the checkpoint inhibitor are administered to the subject sequentially or concurrently as a combination therapy.
7. The method of claim 1 , wherein the cancer is selected from the group consisting of: melanoma, adjuvant melanoma, renal cell carcinoma (RCC), bladder cancer, colorectal cancer (CRC), colon cancer, rectal cancer, anal cancer, breast cancer, triple negative breast cancer (TNBC), HER2-negative breast cancer, BRCA-mutated breast cancer, hematologic malignancies, non-small cell carcinoma, non-small cell lung cancer (NSCLC), small cell lung cancer (SCLC), extensive-stage small cell lung cancer (ES-SCLC), lymphoma (classical Hodgkin's and non-Hodgkin's), primary mediastinal large B-cell lymphoma (PMBCL), T-cell lymphoma, diffuse large B-cell lymphoma, histiocytic sarcoma, follicular dendritic cell sarcoma, interdigitating dendritic cell sarcoma, myeloma, chronic lymphocytic leukemia (CLL), acute myeloid leukemia (AML), small lymphocytic lymphoma (SLL), head and neck cancer, urothelial cancer, merkel cell carcinoma, merkel cell skin cancer, cancer with high microsatellite instability (MSI-H), cancer with mismatch repair deficiency (dMMR), mesothelioma, gastric cancer, gastroesophageal junction cancer (GEJ), gastric adenocarcinoma, neuroendocrine tumors, gastrointestinal stromal tumors (GIST), gastric cardia adenocarcinoma, renal cancer, biliary cancer, cholangiocarcinoma, pancreatic cancer, prostate cancer, adenocarcinoma, squamous cell carcinoma, non-squamous cell carcinoma, cutaneous squamous cell carcinoma (CSCC), ovarian cancer, endometrial cancer, fallopian tube cancer, cervical cancer, peritoneal cancer, stomach cancer, brain cancers, malignant glioma, glioblastoma, gliosarcoma, neuroblastoma, thyroid cancer, adrenocortical carcinoma, oral intraepithelial neoplasia, esophageal cancer, nasal cavity and paranasal sinus squamous cell carcinoma, nasopharynx carcinoma, salivary gland cancer, liver cancer, and hepatocellular cancer (HCC).
8. The method of claim 1 , wherein the antibody, or an antigen-binding fragment thereof, comprises a heavy chain variable domain that is at least 90% identical to the amino acid sequence of SEQ ID NO: 13 and a light chain variable domain that is at least 90% identical to the amino acid sequence of SEQ ID NO:15.
9. The method of claim 8 , wherein the antibody, or antigen-binding fragment thereof, comprises a heavy chain variable domain that is at least 95% identical to the amino acid sequence of SEQ ID NO: 13, and a light chain variable domain that is at least 95% identical to the amino acid sequence of SEQ ID NO:15.
10. The method of claim 1 , wherein the antibody, or the antigen-binding fragment thereof, is administered in combination with an anti-PD-1 antibody or an anti-PD-L1 antibodyat least one additional therapeutic.
11. A method of treating a cancer with primary resistance to checkpoint blockade therapy (CBT) in a subject, the method comprising:
administering to the subject an antibody, or an antigen-binding fragment thereof, that binds pro-transforming growth factor beta 1 (proTGFβ1), wherein the antibody comprises:
a heavy chain complementary determining region 1 (H-CDR1) having an amino acid sequence set forth in SEQ ID NO: 107;
a heavy chain complementary determining region 2 (H-CDR2) having an amino acid sequence set forth in SEQ ID NO: 103;
a heavy chain complementary determining region 3 (H-CDR3) having an amino acid sequence set forth in SEQ ID NO: 6;
a light chain complementary determining region 1 (L-CDR1) having an amino acid sequence set forth in SEQ ID NO: 105;
a light chain complementary determining region 2 (L-CDR2) having an amino acid sequence set forth in SEQ ID NO: 106; and,
a light chain complementary determining region 3 (L-CDR3) having an amino acid sequence set forth in SEQ ID NO: 12, and
administering to the subject an immune checkpoint inhibitor in an amount effective to treat the cancer, wherein the immune checkpoint inhibitor is an anti-programmed cell death protein 1 (PD-1) antibody or an anti-PD-L1 antibody.
12. The method of claim 11 , wherein the antibody, or an antigen-binding fragment thereof, comprises a heavy chain variable domain that is at least 90% identical to the amino acid sequence of SEQ ID NO:13, and a light chain variable domain that is at least 90% identical to the amino acid sequence of SEQ ID NO:15.
13. The method of claim 12 , wherein the antibody, or antigen-binding fragment thereof, comprises a heavy chain variable domain that is at least 95% identical to the amino acid sequence of SEQ ID NO:13, and a light chain variable domain that is at least 95% identical to the amino acid sequence of SEQ ID NO:15.