Cytokine fusion proteins
Provided are cytokine fusion proteins comprising a first cytokine fused to a second cytokine, for example, interleukin-2 (IL-2) or interferon-β (IFN-β) fused to the N-terminus of tumor necrosis factor-α (TNF-α), and related compositions and methods of use thereof for treating cancers, either as standalone agents or in combination with autologous tumor vaccines and/or immune checkpoint modulatory agents.
1. A cytokine fusion protein, comprising a first human cytokine fused to the N-terminus of a second human cytokine, wherein the first cytokine is IL-2 and wherein the second cytokine is TNF-α, wherein the human IL-2 comprises a C125S or C125A mutation and the human TNF-α has increased binding to TNFR1 relative to TNFR2 and B comprises at least one mutation selected from S86T and R32W, including combinations thereof, wherein the first and second cytokines are separated by a stable peptide linker, and wherein the cytokine fusion protein comprises:
(SEQ ID NO: 19)
IL-2(C125S)-(GGGGS)3-TNF-α (S86T);
or
(SEQ ID NO: 20)
IL2(C125A)-(GGGGS)2-TNF-α (S86T);
(SEQ ID NO: 21)
IL2(C125A)-(GGGGS)2-TNF-α (R32W);
(SEQ ID NO: 22)
IL2(C125A)-PAPAP-TNF-α (S86T);
(SEQ ID NO: 23)
IL2(C125A)-PAPAP-TNF-α (R32W);
(SEQ ID NO: 24)
IL2(C125A)-PAEAAAKEAAAKA-TNF-α (S86T);
(SEQ ID NO: 25)
IL2(C125A)-PAEAAAKEAAAKA-TNF-α (R32W);
IL-2(C125S)-(GGGGS)3-TNF-α (R31E, S86T);
or
(SEQ ID NO: 26)
IFN-β-(GGGGS)2-TNF-α.
an amino acid sequence that is at least 95% identical to a sequence selected from SEQ ID NOs: 19-25 and which has a cytokine signaling activity and anti-tumor activity.
2. The fusion protein of claim 1 , comprising, consisting, or consisting essentially of an amino acid sequence selected from SEQ ID NOs: 19-25 and which has a cytokine signaling activity and/or an anti-tumor activity.
3. A method of treating a cancer in a subject in need thereof, comprising administering to the subject a fusion protein of claim 1 .
4. The method of claim 3 , comprising administering the fusion protein to the subject in combination with an autologous tumor cell vaccine from the subject.
5. The method of claim 4 , comprising administering the fusion protein and the autologous tumor vaccine together in the same therapeutic or vaccine composition.
6. The method of claim 5 , comprising administering the fusion protein to the subject in combination with an immune checkpoint modulatory agent.
7. The method of claim 6 , comprising administering the fusion protein and the immune checkpoint modulatory agent together in the same therapeutic or vaccine composition.
8. The method of claim 3 , comprising administering the fusion protein to the subject in combination with an autologous tumor vaccine and an immune checkpoint modulatory agent.
9. The method of claim 8 , comprising administering the fusion protein, the autologous tumor vaccine, and the immune checkpoint modulatory agent together in the same therapeutic or vaccine composition.
10. The method of claim 3 , wherein the cancer is a primary cancer.
11. The method of claim 3 , wherein the cancer is a metastatic cancer.
12. The method of claim 3 , wherein the cancer is selected from one or more of melanoma (e.g., metastatic melanoma), pancreatic cancer, bone cancer, prostate cancer, small cell lung cancer, non-small cell lung cancer (NSCLC), mesothelioma, leukemia (e.g., lymphocytic leukemia, chronic myelogenous leukemia, acute myeloid leukemia, relapsed acute myeloid leukemia), lymphoma, hepatoma (hepatocellular carcinoma), sarcoma, B-cell malignancy, breast cancer, ovarian cancer, colorectal cancer, glioma, glioblastoma multiforme, meningioma, pituitary adenoma, vestibular schwannoma, primary CNS lymphoma, primitive neuroectodermal tumor (medulloblastoma), kidney cancer (e.g., renal cell carcinoma), bladder cancer, uterine cancer, esophageal cancer, brain cancer, head and neck cancers, cervical cancer, testicular cancer, thyroid cancer, and stomach cancer.
13. The method of claim 11 , wherein the metastatic cancer is selected from one or more of:
(a) a bladder cancer which has metastasized to the bone, liver, and/or lungs;
(b) a breast cancer which has metastasized to the bone, brain, liver, and/or lungs;
(c) a colorectal cancer which has metastasized to the liver, lungs, and/or peritoneum;
(d) a kidney cancer which has metastasized to the adrenal glands, bone, brain, liver, and/or lungs;
(e) a lung cancer which has metastasized to the adrenal glands, bone, brain, liver, and/or other lung sites;
(f) a melanoma which has metastasized to the bone, brain, liver, lung, and/or skin/muscle;
(g) a ovarian cancer which has metastasized to the liver, lung, and/or peritoneum;
(h) a pancreatic cancer which has metastasized to the liver, lung, and/or peritoneum;
(i) a prostate cancer which has metastasized to the adrenal glands, bone, liver, and/or lungs;
(j) a stomach cancer which has metastasized to the liver, lung, and/or peritoneum;
(l) a thyroid cancer which has metastasized to the bone, liver, and/or lungs; and
(m) a uterine cancer which has metastasized to the bone, liver, lung, peritoneum, and/or vagina.
14. The method of claim 3 , comprising administering the fusion protein or therapeutic or vaccine composition by subcutaneous, intravenous, intradermal, intra-tumoral, peri-tumoral, or intra-lymph node injection, including any combination thereof.