Anti-tumor therapeutic agents based on B7h receptor ligands
Novel anti-tumor agents comprising at least one ligand of the B7h receptor, wherein the ligand of receptor B7h is loaded in a biocompatible micro- or nano-carrier and is able of binding to receptor B7h and triggering receptor B7h activity.
1. A method of treatment comprising administering to a subject in need thereof suffering from an established tumor a composition comprising an active agent loaded into or onto a biocompatible micro-or nano-carrier, wherein the active agent consists of a ligand of receptor B7h, wherein the ligand loaded into or onto the biocompatible micro-or nano-carrier is capable of exerting cell toxicity in an in vitro B16-F10 cell viability assay, and wherein the ligand comprises
a) a human ICOS protein having the amino acid sequence as set forth in SEQ ID No.: 1 or a B7h binding portion thereof;
b) a human ICOS extracellular domain having the amino acid sequence as set forth in SEQ ID No.: 2 or a B7h binding portion thereof; or
c) a polypeptide having at least 95% sequence identity to the amino acid sequence of the human ICOS protein or B7h binding portion thereof according to a) or to the amino acid sequence of the human ICOS extracellular domain or B7h binding portion thereof according to b), wherein the polypeptide is capable of binding to receptor B7h.
2. The method according to claim 1 , wherein the ligand is hyperglycosylated or conjugated to mannose residues.
3. The method according to claim 1 , wherein the ligand loaded into or onto a biocompatible micro-or nano-carrier is administered by injection or infusion.
4. The method according to claim 1 , wherein the ligand is fused or conjugated to a stabilizing molecule.
5. The method according to claim 4 , wherein the stabilizing molecule is selected from: a human Fc antibody domain, polyethylene glycols, poly-L-lysine citramide, styrenemaleic acid anhydride, and polyhydroxypropylmetacrylamide.
6. The method according to claim 1 , wherein the ligand comprises the amino acid sequence as set forth in SEQ ID No.: 3.
7. The method according to claim 1 , wherein the biocompatible micro-or nano-carrier is selected from micro-or nano-particles, micro-or nano-capsules, micro-or nano-vesicles, micro-or nano-bubbles, nanoemulsions, nanosuspensions, nanohydrogels, micelles, dendrimers, quantum dots, liposomes, and carbon derivatives.
8. The method according to claim 7 , wherein the micro-or nano-particles are made of cyclodextrin polymer, poly (lactide-co-glycolic acid), polycaprolactone, (PCL), polylactic acid (PLA), poly (glycolide), chitosan, alginate, starch, collagen, albumin, silica or metal.
9. The method according to claim 7 , wherein the micro-or nano-particles are made of cyclodextrin polymer or poly (lactide-co-glycolic acid).
10. The method according to claim 9 , wherein the tumor is melanoma or glioblastoma.
11. A method of treatment comprising administering to a subject in need thereof suffering from an established tumor a pharmaceutical composition comprising an active agent loaded into or onto a biocompatible micro-or nano-carrier, wherein the active agent consists of a ligand of receptor B7h, wherein the ligand loaded into or onto a biocompatible micro-or nano-carrier is capable of exerting cell toxicity in an in vitro B16-F10 cell viability assay, and wherein the ligand comprises
a) a human ICOS protein having the amino acid sequence as set forth in SEQ ID No.: 1 or a B7h binding portion thereof;
b) a human ICOS extracellular domain having the amino acid sequence as set forth in SEQ ID No.: 2 or a B7h binding portion thereof; or
c) a polypeptide having at least 95% sequence identity to the amino acid sequence of the human ICOS protein or B7h binding portion thereof according to a) or to the amino acid sequence of the human ICOS extracellular domain or B7h binding portion thereof according to b), wherein the polypeptide is capable of binding to receptor B7h.
12. The method according to claim 11 , wherein the ligand is fused or conjugated to a stabilizing molecule.
13. The method according to claim 11 , wherein the ligand comprises an amino acid sequence as set forth in SEQ ID No.: 3.
14. The method according to claim 11 , wherein the biocompatible micro-or nano-carrier is selected from micro-or nano-particles, micro-or nano-capsules, micro-or nano-vesicles, micro-or nano-bubbles, nanoemulsions, nanosuspensions, nanohydrogels, micelles, dendrimers, quantum dots, liposomes, and carbon derivatives.
15. The method according to claim 11 , wherein the micro-or nano-particles are made of cyclodextrin polymer or poly (lactide-co-glycolic acid).
16. The method according to claim 15 , wherein the tumor is melanoma or glioblastoma.
17. A method of inhibiting tumor angiogenesis comprising administering to a subject in need thereof suffering from a tumor a ligand of receptor B7h, wherein the ligand of B7h receptor has been loaded into or onto a biocompatible micro-or nano-carrier, wherein the ligand loaded into or onto the biocompatible micro-or nano-carrier is capable of exerting cell toxicity in an in vitro B16-F10 cell viability assay, and wherein the ligand comprises
a) a human ICOS protein having the amino acid sequence as set forth in SEQ ID No.: 1 or a B7h binding portion thereof;
b) a human ICOS extracellular domain having the amino acid sequence as set forth in SEQ ID No.: 2 or a B7h binding portion thereof; or
c) a polypeptide having at least 95% sequence identity to the amino acid sequence of the human ICOS protein or B7h binding portion thereof according to a) or to the amino acid sequence of the human ICOS extracellular domain or B7h binding portion thereof according to b), wherein the polypeptide is capable of binding to receptor B7h.
18. The method according to claim 17 , wherein the ligand is fused or conjugated to a stabilizing molecule selected from the group consisting of: a human Fc antibody domain, polyethylene glycols, poly-L-lysine citramide, styrenemaleic acid anhydride, and polyhydroxypropylmetacrylamide.
19. The method according to claim 17 , wherein the ligand comprises the amino acid sequence as set forth in SEQ ID No.: 3.
20. The method according to claim 17 , wherein the micro-or nano-particles are made of cyclodextrin polymer, poly (lactide-co-glycolic acid), polycaprolactone, (PCL), polylactic acid (PLA), poly (glycolide), chitosan, alginate, starch, collagen, albumin, silica or metal.
21. The method according to claim 17 , wherein the tumor is melanoma or glioblastoma.