Composition for and Method of Treating Hepatic Tissue Injury
Compositions for and methods of treating liver injury are provided. Said compositions comprise MG53 or express MG53. Said compositions can be used for treating chronic or acute injured liver tissue and can be administered systemically, locally, or both.
1 ) A method of treating liver injury, the method comprising administering to a subject in need thereof an effective amount of MG53 in a dosage form.
2 ) The method of claim 1 , wherein the MG53 is exogenous MG53.
3 ) The method of claim 1 , wherein the dosage form a) releases or provides MG53; b) is a biological dosage form that releases MG53 or enables expression of MG53 followed by release of MG53; c) enables expression of MG53 followed by release of MG53; d) comprises exogenously added MG53; e) is an autologous serum dosage form comprising cells that express MG53; f) is autologous serum dosage form comprising a viral vector that causes cells to express MG53; g) is autologous blood serum comprising added exogenous MG53.
4 ) The method of claim 1 , wherein the MG53 is administered intramuscularly, intravenously, subcutaneously, orally, systemically, or a combination of two or more thereof.
5 ) The method of claim 1 , wherein the dosage form is selected from the group consisting of a liquid, solution, suspension, gel, cream, ointment, implant, explant, nanoparticle(s), and microparticle(s).
6 ) The method of claim 1 , wherein the dosage form is administered acutely, chronically, every other day, five times per week, four times per week, three times per week, two times per week, once daily, twice daily, one to four times daily, continuously, weekly, monthly, bimonthly, quarterly, semiannually, annually, or as frequently or infrequently as needed.
7 ) The method of claim 1 , wherein said injury is selected from the group consisting of an acute liver injury and chronic liver injury.
8 ) The method of claim 1 , wherein said injury is caused by one or more of liver preservation, liver perfusion, stroke, hypoxia, liver transplantation, ischemia, open heart surgery, blood clot, loss of blood circulation to the liver, drug-induced liver injury (DILI), cirrhosis of the liver, alcoholic liver disease, post-graft dysfunction, diabetes, fatty liver, hypercholesterolemia, cholestatic liver, DILI, hepatitis A, hepatitis B, hepatitis C, hepatitis D, hepatitis E, viral hepatitis, viral infection of the liver, Yellow Fever, American Plague, autoimmune hepatitis, or other such life-threatening (or end-stage) diseases.
9 ) A cotherapeutic or adjunctive method of treating injured liver tissue, the method comprising administering to a subject in need thereof an effective amount of MG53 and an effective amount of one or more other active ingredients, which are suitable for treating a liver disease, disorder, injury or condition.
10 ) The method of claim 9 , wherein the MG53 is exogenous MG53.
11 ) The method of claim 9 , wherein the MG53 is in a dosage form that a) releases or provides MG53; b) is a biological dosage form that releases MG53 or enables expression of MG53 followed by release of MG53; c) enables expression of MG53 followed by release of MG53; d) comprises exogenously added MG53; e) is an autologous serum dosage form comprising cells that express MG53; f) is autologous serum dosage form comprising a viral vector that causes cells to express MG53; g) is autologous blood serum comprising added exogenous MG53.
12 ) The method of claim 11 , wherein the dosage form is selected from the group consisting of a liquid, solution, suspension, gel, cream, ointment, implant, explant, nanoparticle(s), and microparticle(s).
13 ) The method of claim 11 , wherein the dosage form is administered acutely, chronically, every other day, five times per week, four times per week, three times per week, two times per week, once daily, twice daily, one to four times daily, continuously, weekly, monthly, bimonthly, quarterly, semiannually, annually, or as frequently or infrequently as needed.
14 ) The method of claim 9 , wherein the MG53 is administered intramuscularly, intravenously, subcutaneously, orally, systemically, or a combination of two or more thereof.
15 ) The method of claim 9 , wherein the injured liver tissue is caused by acute liver injury and chronic liver injury.
16 ) The method of claim 9 , wherein the injured liver tissue is caused by one or more of liver preservation, liver perfusion, stroke, hypoxia, liver transplantation, ischemia, open heart surgery, blood clot, loss of blood circulation to the liver, drug-induced liver injury (DILI), cirrhosis of the liver, alcoholic liver disease, post-graft dysfunction, diabetes, fatty liver, hypercholesterolemia, cholestatic liver, DILI, hepatitis A, hepatitis B, hepatitis C, hepatitis D, hepatitis E, viral hepatitis, viral infection of the liver, Yellow Fever, American Plague, autoimmune hepatitis, or other such life-threatening (or end-stage) diseases.
17 ) A method of preventing hepatic tissue injury, the method comprising administering to a subject at risk of developing said hepatic tissue injury an effective amount of exogenous MG53 in a dosage form.
18 ) The method of claim 17 , wherein the dosage form a) releases or provides MG53; b) is a biological dosage form that releases MG53 or enables expression of MG53 followed by release of MG53; c) enables expression of MG53 followed by release of MG53; d) comprises exogenously added MG53; e) is an autologous serum dosage form comprising cells that express MG53; f) is autologous serum dosage form comprising a viral vector that causes cells to express MG53; g) is autologous blood serum comprising added exogenous MG53.
19 ) The method of claim 17 , wherein the MG53 is administered intramuscularly, intravenously, subcutaneously, orally, systemically, or a combination of two or more thereof.
20 ) The method of claim 17 , wherein the dosage form is selected from the group consisting of a liquid, solution, suspension, gel, cream, ointment, implant, explant, nanoparticle(s), and microparticle(s).
21 ) The method of claim 17 , wherein the dosage form is administered acutely, chronically, every other day, five times per week, four times per week, three times per week, two times per week, once daily, twice daily, one to four times daily, continuously, weekly, monthly, bimonthly, quarterly, semiannually, annually, or as frequently or infrequently as needed.
22 ) The method of claim 17 , wherein said injury is caused by one or more of liver perfusion, stroke, hypoxia, liver transplantation, ischemia, open heart surgery, blood clot, loss of blood circulation to the liver, drug-induced liver injury (DILI), cirrhosis of the liver, alcoholic liver disease, post-graft dysfunction, diabetes, fatty liver, hypercholesterolemia, cholestatic liver, DILI, hepatitis A, hepatitis B, hepatitis C, hepatitis D, hepatitis E, viral hepatitis, viral infection of the liver, Yellow Fever, American Plague, autoimmune hepatitis, or other such life-threatening (or end-stage) diseases.