Protease activated cytokines
Provided herein are chimeric nucleic acid sequences encoding chimeric polypeptides. Also provided herein are chimeric polypeptides. Further provided herein are methods of treating a subject with or at risk of developing a cancer. The methods comprise selecting a subject with or at risk of developing a cancer, and administering to the subject an effective amount of the chimeric polypeptides provided herein.
1. A method of treating a subject with a cancer, the method comprising:
(a) selecting a subject with cancer; and
(b) administering to the subject an effective amount of a chimeric polypeptide, wherein the chimeric polypeptide comprises (i) a first polypeptide comprising an interleukin-2 (IL-2) polypeptide or a fragment of an IL-2 polypeptide; (ii) a second polypeptide comprising a protease-cleavable sequence; and (ii) a third polypeptide comprising a blocking polypeptide, wherein the blocking polypeptide blocks the activity of the IL-2 polypeptide or fragment of the IL-2 polypeptide, wherein the protease cleavable sequence is cleaved by PSA or a matrix metalloproteinase (MMP), wherein the cancer is selected from the group consisting of prostate cancer, lung cancer, colon cancer, breast cancer and skin cancer and wherein the chimeric polypeptide is selected from the group consisting of SEQ ID NO: 31; SEQ ID NO: 32; SEQ ID NO: 33; SEQ ID NO: 34; SEQ ID NO: 35; SEQ ID NO: 36; SEQ ID NO: 37; SEQ ID NO: 38; SEQ ID NO: 39; SEQ ID NO: 40; SEQ ID NO: 41; SEQ ID NO: 42; SEQ ID NO: 43; SEQ ID NO: 44; SEQ ID NO: 45; SEQ ID NO: 46; SEQ ID NO: 47; SEQ ID NO: 48; SEQ ID NO: 49; SEQ ID NO: 50; a chimeric polypeptide comprising SEQ ID NO: 45, wherein amino acids 154-171 of SEQ ID NO: 45 are replaced with amino acids 170-201 of SEQ ID NO: 38; and a chimeric polypeptide comprising SEQ ID NO: 48, wherein amino acids 154-176 of SEQ ID NO: 48 are replaced with amino acids 170-201 of SEQ ID NO: 38.
2. The method of claim 1 , wherein the blocking polypeptide is an alpha chain of the IL-2 receptor (IL-2Rα).
3. The method of claim 1 , wherein the chimeric polypeptide further comprises a histidine tag.
4. The method of claim 1 , wherein the chimeric polypeptide comprises a linker sequence.
5. The method of claim 4 , wherein the linker sequence is selected from the group consisting of GGGGS (SEQ ID NO:6), GSGSGS (SEQ ID NO:7), and G(SGGG) 2 SGGT (SEQ ID NO:8).
6. The method of claim 1 , wherein the MMP is matrix metalloproteinase 2 (MMP2) or matrix metalloproteinase 9 (MMP9).