Patent Application
20190328848
The present invention relates to the effect of plasminogen in the prevention and treatment of nephropathy, thereby providing a brand new therapeutic strategy for treating nephropathy and its related conditions caused by different reasons.
Nephropathy is a renal structural change and dysfunction caused by various reasons. Nephropathy causes injuries to a structure of a renal tissue, thereby affecting its function. Nephropathy can be primary, such as glomerulonephritis, chronic pyelonephritis, nephrotic syndrome, renal insufficiency, glomerular sclerosis, glomerular mesangial hyperplasia, tubulointerstitial lesions, renal tubular atrophy and the like caused by an infection, an inflammation, an allergic reaction, and the like; and can also be secondary to other diseases, for instance, nephropathy can be caused by ischemia, metabolic disorders such as a glucose metabolism disorder and a fat metabolism disorder, and other diseases such as tumors.
For instance, hypertension, diabetes mellitus, atherosclerosis, and other diseases are often accompanied by nephropathy. Hypertension is one of common chronic diseases, the main manifestation of which is increased systemic arterial pressure. If the blood pressure of hypertensive patients is not well controlled, complications are easily developed such as cerebral stroke, coronary heart disease, retinopathy, and a chronic kidney disease. In addition, prolonged hypertension can affect more and more tissues and organs. Therefore, we should strengthen and prevent hypertension and its complications, so as to reduce the harm of hypertension[1].
Diabetic nephropathy (DN) is a common and important complication of diabetes mellitus, and is a major cause of mortality and disability in diabetic patients. If the diagnosis and treatment is not timely, when DN develops to end-stage renal disease, only dialysis or even kidney transplantation will be adopted. The main pathological features of DN in an early stage are glomerular hypertrophy, thickening of glomerular and tubular basement membrane, and progressive accumulation of extracellular matrix in the mesangial area; and those in a later stage are glomerular and tubulointerstitial fibrosis. Early clinical manifestations comprise a reduced glomerular filtration rate, followed by microalbuminuria, an elevated arterial blood pressure, proteinuria, and fluid retention, ultimately leading to renal failure[2].
Diabetic nephropathy is a diabetic microvascular complication, the development of which is related to factors such as hyperglycemia and oxidative stress, wherein hyperglycemia is an important factor in the production of microalbuminuria[3]. Microalbuminuria may predict the progression of diabetic nephropathy. Diabetic atherosclerosis is a macrovascular complication of diabetes mellitus, which is closely related to hyperglycemia, vascular endothelial dysfunction, insulin resistance, and other factors. Recent studies have found that proteinuria is closely related to atherosclerosis[4].
In developed countries, diabetic nephropathy and hypertensive renal arteriolosclerosis have become the main causes of a chronic kidney disease. In China, these two diseases still rank behind primary glomerulonephritis in various causes, but there is a significant uptrend in recent years.
Systemic allergic diseases, such as systemic sclerosis, systemic lupus erythematosus, systemic vasculitis, anaphylactoid purpura, polymyositis, and thrombotic mlcroangiopathy, often affect the kidneys.
Most drugs and their metabolites are excreted by the kidneys, and thus the incidence of a drug-induced renal injury is very high. Studies have shown that the incidence of drug-induced acute tubular necrosis (ATN) or acute interstitial nephritis (AIN) is up to 18.3%, and the incidence of an antibiotic-induced renal injury is up to 36%[5].
Anti-infective drugs, such as aminoglycoside antibiotics, are widely used to treat Grain-negative bacterial infections, but nephrotoxicity limits their clinical application[6].
The antiviral agent, aciclovir (ACV), is a cyclic analogue of deoxyguanosine against herpes virus. Parenteral administration of large doses of aciclovir can cause acute renal failure (ARF) in 10% to 48% of patients, which may be caused by renal obstruction due to aciclovir deposition in renal tubules, toxic immune response or hypersensitivity reaction, etc.[7] Adedovir (ADV) and cidofovir (CDV), as nucleoside analogues, are commonly used clinically to treat hepatitis B and AIDS. When nephrotoxicity occurs, it is usually manifested as tubular necrosis and interstitial fibrosis [8].
An immunosuppressive agent, such as cyclosporine A (CsA), is widely used in organ transplantation and treatment of an autoimmune disease as an immunosuppressive agent. It has been reported that about 30% of patients treated with CsA develop moderate to severe renal dysfunction. The mechanism of a renal injury comprises ischemia due to renal vasoconstriction and an endothelial cell injury, and the direct toxic effect of CsA on renal tubular epithelial cells[9].
Anti-tumor drugs, such as cisplatin (Cis) as a cell proliferation inhibitor, are widely used in the treatment of testicular cancer, ovarian cancer, prostate cancer, lung cancer, bone cancer, head and neck cancer, and other solid tumors. Cis has a high anti-tumor efficiency, but it also has dose-dependent nephrotoxicity, etc.[10], which is substantially manifested as azotemia, polyuria and renal failure, characterized by injuries of the glomeruli and renal tubules.
A non-steroidal anti-inflammatory drug, such as acetylsalicylic acid (ASA), is the most widely used antipyretic and analgesic anti-inflammatory drug in the world. The dose used for antipyretic and analgesic purposes rarely causes adverse reactions; however, the long-term heavy drug use can easily lead to side effects, the manifestations of which are escape of potassium ions from renal tubular cells due to decoupling of oxidative phosphorylation, resulting in potassium deficiency and excessive excretion of uric acid in urine, and in the case of a greater injury, interstitial nephritis, renal papillary necrosis, and renal hypofunction may occur
Aristolochic acid (AA) as an active component of a natural product is a nephrotoxin derived from plants of Aristolochiaceae, and is the cause of the well-known aristolochic acid nephropathy (AAN)[12]. AA induces a renal injury mainly at sites of renal tubules, results in cell apoptosis or death, and inhibits the proliferation of renal interstitial fibroblasts, leading to renal tubular atrophy and oligo-cellular interstitial fibrosis.
Diuretics are drugs that increase urine output by inhibiting the reabsorption of water and electrolytes in renal tubules. All kinds of diuretics have potential nephrotoxicity, and might cause a renal injury after application. The nephrotoxicity caused by diuretics is related to the cytotoxicity, immune response, an allergic reaction, a metabolism disorder and other adverse reactions caused by such kinds of drugs, and the diuretics should be avoided to be used in combination with nephrotoxic drugs to prevent aggravation of the renal injury. In addition, there are a variety of drugs that can cause a renal injury, for instance, sulfonamides often cause the formation of sulfonamide crystals blocking the ureter and thus cause obstructive nephropathy[13]. Hypolipidemic drugs such as statins can cause rhabdomyolysis, which in turn leads to tubular necrosis[14].
Nephropathy will cause partial or total loss of renal function in a later stage, which is a pathological state leading to renal failure. Renal failure can be divided into acute renal failure and chronic renal failure. The condition of acute renal failure progresses rapidly, and generally due to insufficient supply of blood in the kidney, impaired renal function caused by obstruction due to a certain factor, or a toxin-induced renal injury, acute renal failure occurs. Chronic renal failure is mainly caused by long-term nephropathy, and as time goes on and the disease progresses, the renal function gradually declines, leading to the occurrence of renal failure.
Chronic renal failure refers to slow progressive renal function impairment caused by various kidney diseases, ultimately causing uremia and complete loss of renal function, and leading to a series of clinical symptoms as well as a clinical syndrome composed of a biochemical endocrine disorder and other metabolism disorders; and the interval from primary onset to start of renal failure may be several years to more than a decade.
Uremia is the end stage of chronic renal failure. Chronic renal failure is a result of renal injury and progressive deterioration caused by various causes. Common basic diseases comprise primary glomerulonephritis, tubulointerstitial nephritis, diabetic nephropathy, etc. Its clinical manifestations are mainly renal hypofunction, metabolic waste retention, water, electrolyte and acid-base imbalance, and thus failure of maintaining stability of the environment in the body. Chronic renal failure can be divided into four stages according to the degree of renal function impairment: compensatory stage of renal insufficiency, decompensatory stage of renal insufficiency, renal failure stage, and uremia stage.
In an early stage of chronic renal insufficiency, only the symptoms of primary diseases are observed clinically, and only a decrease in creatinine clearance can be observed in an examination. In patients in the compensatory stage of uremia, renal function often deteriorates abruptly under stress, accompanied by water, electrolyte and acid-base metabolism disorder, protein, glucose, fat and vitamin metabolism disorders, loss of appetite or dyspepsia; in the case of condition aggravated, anorexia, nausea, vomiting or diarrhea and other gastrointestinal symptoms, and other early symptoms of uremia may occur, clinically known as reversible uremia. Once the stress factors are removed, renal function can often be restored to the compensatory stage. If the condition progresses to a point where the “intact” nephron is unable to meet the minimum requirements of the body, uremic symptoms will gradually appear even without stress factors, and are manifested as systemic symptoms such as a water and electrolyte metabolism disorder, accumulation of metabolites in the body, etc., and moderate symptoms of the cardiovascular system, respiratory system, and blood system.
The drug therapies of chronic renal insufficiency mainly focuses on three aspects: relieving symptoms, delaying disease progression, and preventing and treating complications, specifically for instance, correction of acidosis as well as water and electrolyte disorder, treatment of hypertension, prevention and treatment of infections, treatment of hyperlipemia, and treatment of complications of the cardiovascular, respiratory, and blood systems, as well as alternative dialysis treatment for uremia at the same time, such as hemodialysis or peritoneal dialysis, or kidney transplantation.
“Acute renal injury (AKI)” is a new term proposed in recent years, which is used to replace the acute renal failure (ARF) used for many years, and has been widely recognized. It is a common clinical syndrome, which is substantially manifested by rapid decrease of renal function and accumulation of metabolic wastes. The incidence of AKI is high and is increasing year by year. It has been reported in foreign countries that the incidence of AKI has increased from 0.65‰ to 5‰ in the past decade, and the incidence of AKI requiring dialysis is 0.295‰[15-15]. The incidence of AKI in inpatients is 1.9%, and can be up to 60% in intensive care units[17]. Currently, there is no specific drug for AKI treatment, and renal replacement therapy is required for severe patients[18]. The prognosis of AKI is also not optimistic. The ATN and RENAL studies[19-20] reported that the mortality rates of AKI in critically ill patients were 53.0% and 44.7%, respectively, and the surviving patients were also prone to develop to chronic nephropathy and even to end-stage nephropathy[21]. Therefore, AKI has attracted more and more attention from clinicians.
For a renal tissue injury caused by various reasons, people have been eager to find more effective therapeutic drugs. The studies of the present invention found that plasminogen can promote repair of an injured renal tissue and recovery of renal function, and can further inhibit apoptosis of an injured renal tissue and reduce its fibrosis. Therefore, plasminogen is expected to become a novel drug for treating kidney diseases.
The present invention relates to the following items:
In one aspect, the present invention relates to: Item 1. A method for preventing and/or treating a drug-induced renal tissue injury and its related conditions in a subject, comprising administering an effective amount of plasminogen to the subject.
Item 2. The method of item 1, wherein the drug is a nephrotoxic drug.
Item 3. The method of item 1 or 2, wherein the drug is a renal excretory drug.
Item 4. The method of any of items 1 to 3, wherein the drug comprises a chemotherapeutic drug, an antihypertensive drug, a hypolipidemic drug, a hypoglycemic drug, a nonsteroid anti-inflammatory drug, an antibiotic drug, and an antiviral drug.
Item 5. The method of any one of items 1 to 4, wherein the plasminogen promotes repair of an injured renal tissue.
Item 6. The method of any one of items 1 to 5, wherein the plasminogen alleviates fibrosis of the injured renal tissue.
Item 7. The method of any one of items 1 to 6, wherein the plasminogen alleviates apoptosis of the injured renal tissue.
Item 8. The method of any one of items 1 to 7, wherein the drug-induced renal tissue injury in the subject is an acute renal tissue injury.
Item 9. The method of any one of items 1 to 7, wherein the drug-induced renal tissue injury in a subject is a chronic renal tissue injury.
Item 10. The method of any one of items 1 to 9, wherein the plasminogen promotes recovery of renal function.
In another aspect, the present invention relates to: Item 11. A method for protecting a subject's kidney from drug-induced injury or alleviating the drug-induced injury to the kidney, comprising administering an effective amount of plasminogen to the subject before, simultaneously with, and/or after administration of the drug.
In another aspect, the present invention relates to: Item 12. A method for preventing and/or treating a nephropathy-induced renal tissue injury and its related conditions in a subject, comprising administering an effective amount of plasminogen to the subject.
Item 13. The method of item 13, wherein the drug is cisplatin.
Item 14. The method of item 12 or 13, wherein the renal tissue injury comprises a renal tissue injury caused by nephropathy due to an infection, an inflammation, an allergic reaction, autoimmunity, ischemia, microangiopathy, a thrombus, a trauma, a radiation injury, a glucose metabolic disorder, an electrolyte disorder, a fat metabolism disorder, and tumors.
Item 15. The method of any one of items 12 to 14, wherein the nephropathy is nephropathy caused by a systemic disease selected from: hypertension, diabetes mellitus, atherosclerosis, systemic sclerosis, systemic lupus erythematosus, hyperlipemia, non-Hodgkin's lymphoma, multiple myeloma, systemic vasculitis, anaphylactoid purpura, polymyositis, and thrombotic microangiopathies.
Item 16. The method of any one of items 12 to 15, wherein the nephropathy is a chronic kidney disease.
Item 17. The method of any one of items 12 to 16, wherein the chronic kidney disease is chronic glomerulonephritis, chronic pyelonephritis, nephrotic syndrome, renal insufficiency or uremia.
Item 18. The method of item 17, wherein the chronic kidney disease is glomerular sclerosis, glomerular mesangial hyperplasia; tubulointerstitial lesions, renal interstitial fibrosis, and renal tubular atrophy.
Item 19. The method of any one of items 12 to 18, wherein the chronic kidney disease is a drug-induced chronic renal injury.
Item 20. The method of item 19, wherein the chronic kidney disease is a chronic renal injury induced by a chemotherapeutic drug, an antihypertensive drug, a hypolipidemic drug, a hypoglycemic drug, a nonsteroid anti-inflammatory drug, an antibiotic drug, and an antiviral drug.
Item 21. The method of item 20, wherein the chemotherapeutic drug is cisplatin.
Item 22. The method of any one of items 12 to 15, wherein the nephropathy is an acute kidney disease.
Item 23. The method of any one of items 12 to 15, wherein the acute kidney disease is acute glomerulonephritis, acute pyelonephritis, an acute renal injury, acute renal failure, acute renal insufficiency, and acute tubular necrosis.
Item 24. The method of item 22 or 23, wherein the acute renal injury is an acute renal injury induced by a chemotherapeutic drug.
In another aspect, the present invention relates to: Item 25. A method for preventing and/or treating a chronic renal injury, comprising administering a prophylactically and/or therapeutically effective amount of plasminogen to a subject.
Item 26. The method of item 25, wherein the chronic renal injury is a renal tissue injury caused by a chronic kidney disease.
Item 27. The method of item 26, wherein the chronic kidney disease is chronic glomerulonephritis, chronic pyelonephritis, nephrotic syndrome, renal insufficiency, or uremia.
Item 28. The method of item 26, wherein the chronic kidney disease is glomerular sclerosis, glomerular mesangial hyperplasia, tubulointerstitial lesions, renal interstitial fibrosis, renal failure, and renal tubular atrophy.
Item 29. The method of any one of items 25 to 28, wherein the chronic renal injury is a renal tissue injury accompanied by a systemic disease.
Item 30. The method of item 29, wherein the systemic disease is selected from: hypertension, diabetes mellitus, atherosclerosis, systemic sclerosis, systemic lupus erythematosus, hyperlipemia, non-Hodgkin's lymphoma, multiple myeloma, systemic vasculitis, anaphylactoid purpura, polymyositis, and thrombotic microangiopathies.
Item 31. The method of item 30, wherein the systemic disease is systemic sclerosis.
Item 32. The method of any one of items 1 to 31, wherein the plasminogen can promote repair of an injured renal tissue.
Item 33. The method of any one of items 1 to 31, wherein the plasminogen can reduce fibrosis of the injured renal tissue.
Item 34. The method of any one of items 1 to 31, wherein the plasminogen can promote expression of apoptosis inhibitory protein Bcl-2 and inhibit apoptosis in a renal tissue.
Item 35. The method of any one of items 1 to 31, wherein the plasminogen can promote recovery of renal function.
Item 36. The method of item 35, wherein the plasminogen can promote clearance of urea nitrogen and/or creatinine by the kidney.
In another aspect, the present invention relates to: Item 37. A method for preventing and/or treating an acute renal injury, comprising administering a prophylactically and/or therapeutically effective amount of plasminogen to a subject in a need thereof.
Item 38. The method of item 37, wherein the acute renal injury is acute glomerulonephritis, acute pyelonephritis, acute renal failure, acute renal insufficiency, and acute tubular necrosis.
Item 39. The method of item 37 or 38, wherein the acute renal injury is an acute renal injury induced by a chemotherapeutic drug.
Item 40. The method of item 39, wherein the chemotherapeutic drug is cisplatin.
Item 41. The method of any one of items 37 to 40, wherein the plasminogen can reduce fibrosis of the injured renal tissue.
Item 42. The method of any one of items 37 to 40, wherein the plasminogen can promote expression of apoptosis inhibitory protein Bcl-2 and inhibit apoptosis in a renal tissue.
Item 43. The method of any one of items 37 to 40, wherein the plasminogen can promote recovery of renal function.
Item 44. The method of item 43, wherein the plasminogen can promote clearance of urea nitrogen and/or creatinine by the kidney.
In another aspect, the present invention relates to: Item 45. A method for preventing and/or treating a renal tissue injury related condition, comprising administering a prophylactically and/or therapeutically effective amount of plasminogen to a subject in a need thereof.
Item 46. The method of item 45, wherein the renal tissue injury related condition is selected from: hematuria, proteinuria, cylindruria, decreased glomerular filtration rate, oliguria, anuria, metabolite retention, water, electrolyte and acid-base imbalance, renal fibrosis, renal failure, and uremia.
Item 47. The method of any one of items 1 to 46, wherein the plasminogen has at least 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98% or 99% sequence identity with SEQ ID No. 2, 6, 8, 10 or 12, and still has the plasminogen activity.
Item 48. The method of any one of items 1 to 47, wherein the plasminogen is a protein that has 1-100, 1-90, 1-80, 1-70, 1-60, 1-50, 1-45, 1-40, 1-35, 1-30, 1-25, 1-20, 1-15, 1-10, 1-5, 1-4, 1-3, 1-2 or 1 amino acid added, deleted and/or substituted in SEQ ID No. 2, 6, 8, 10 or 12, and still has the plasminogen activity.
Item 49. The method of any one of items 1 to 48, wherein the plasminogen is a protein that comprises a plasminogen active fragment and still has the plasminogen activity.
Item 50. The method of any one of items 1 to 49, wherein the plasminogen is selected from Glu-plasminogen, Lys-plasminogen, mini-plasminogen, micro-plasminogen, delta-plasminogen or their variants that retain the plasminogen activity.
Item 51. The method of any one of items 1 to 50, wherein the plasminogen is administered in combination with one or more drugs selected from an antihypertensive drug, a hypolipidemic drug, an antibiotic drug, an anticoagulant drug, a thrombolytic drug, a diuretic drug, an anti-tumor drug, a hypoglycemic drug, a non-steroidal anti-inflammatory drug, an immunomodulatory drug, an anti-infective drug, an antiviral drug, a hormone, and an active ingredient of a natural product.
Item 52. The method of any one of items 1 to 51, wherein the plasminogen is a natural or synthetic human plasminogen, or a variant or fragment thereof that still retains the plasminogen activity.
Item 53. The method of any one of items 1 to 51, wherein the plasminogen is an ortholog of human plasminogen from a primate or a rodent, or a variant or fragment thereof that still retains the plasminogen activity.
Item 54. The method of any one of items 1 to 53, wherein the amino acids of the plasminogen are as shown in SEQ ID No. 2, 6, 8, 10 or 12.
Item 55. The method of any one of items 1 to 54, wherein the plasminogen is a natural human plasminogen.
Item 56. The method of any one of items 1 to 55, wherein the subject is a human.
Item 57. The method of any one of items 1 to 26, wherein the subject has a lack or deficiency of plasminogen.
Item 58. The method of item 57, wherein the lack or deficiency is congenital, secondary and/or local.
In another aspect, the present invention relates to: Item 59. A plasminogen for use in the method of any one of items 1 to 58.
In another aspect, the present invention relates to: Item 60. A pharmaceutical composition, comprising a pharmaceutically acceptable carrier and the plasminogen for use in the method of any one of items 1 to 58.
In another aspect, the present invention relates to: Item 61. A preventive or therapeutic kit comprising: (i) the plasminogen for use in the method of any one of items 1 to 58, and (ii) a means for delivering the plasminogen to the subject.
Item 62. The kit of item 61, wherein the means is a syringe or a vial.
Item 63. The kit of item 61 or 62, further comprising a label or an instruction for use indicating the administration of the plasminogen to the subject to implement the method of any one of items 1 to 58.
In another aspect, the present invention relates to: Item 64. An article of manufacture, comprising:
a container comprising a label; and
(i) the plasminogen for use in the method of any one of items 1 to 58 or a pharmaceutical composition comprising the plasminogen, wherein the label indicates the administration of the plasminogen or the composition to the subject to implement the method of any one of items 1 to 58.
Item 65. The kit of any one of items 61 to 63 or the article of manufacture of item 64, further comprising one or more additional means or containers containing other drugs.
Item 66. The kit or the article of manufacture of item 65, wherein the other drugs are selected from a group of: a hypolipidemic drug, an anti-platelet drug, an antihypertensive drug, a vasodilator, a hypoglycemic drug, an anticoagulant drug, a thrombolytic drug, a hepatoprotective drug, an anti-arrhythmia drug, a cardiotonic drug, a diuretic drug, an anti-infective drug, an antiviral drug, an immunomodulatory drug, an inflammatory regulatory drug, an anti-tumor drug, a hormone drug, and thyroxine.
The present invention further relates to the use of plasminogen for implementing the method of any one of items 1 to 58.
The present invention further relates to the use of plasminogen in the preparation of a medicament, a pharmaceutical composition, an article of manufacture, and a kit for the method of any one of items 1 to 58.
The present invention further relates to the following items:
In one aspect, the present invention relates to: Item 1. A method for preventing or treating a renal tissue injury in a subject, comprising administering an effective amount of plasminogen to the subject, wherein the subject has a risk of the renal tissue injury, is suspected of having the renal tissue injury or suffers from the renal tissue injury.
Item 2. The method of item 1, wherein the renal tissue injury comprises a renal tissue injury caused by an infection, an inflammation, an allergic reaction, autoimmunity, ischemia, a thrombus, a trauma, a radiation injury, a glucose metabolic disorder, a fat metabolism disorder, and a cancer.
Item 3. The method of item 1 or 2, wherein the renal tissue injury is a renal tissue injury caused by a systemic disease selected from hypertension, diabetes mellitus, atherosclerosis, systemic sclerosis, systemic lupus erythematosus, hyperlipemia, non-Hodgkin's lymphoma, multiple myeloma, systemic vasculitis, anaphylactoid purpura, polymyositis, and thrombotic microangiopathies.
Item 4. The method of item 1 or 2, wherein the renal tissue injury is a renal tissue injury caused by a chronic kidney disease.
Item 5. The method of item 4, wherein the chronic kidney disease is chronic glomerulonephritis, chronic pyelonephritis, nephrotic syndrome, renal insufficiency, renal failure or uremia.
Item 6. The method of item 1 or 2, wherein the chronic kidney disease is a drug-induced chronic renal injury.
Item 7. The method of item 6, wherein the drug comprises a chemotherapeutic drug, an antihypertensive drug, a hypolipidemic drug, a hypoglycemic drug, a nonsteroid anti-inflammatory drug, an antibiotic drug, and an antiviral drug.
Item 8. The method of item 7, wherein the drug is a chemotherapeutic drug, in particular cisplatin.
In another aspect, the present invention relates to: Item 9. A method for preventing or treating an acute renal tissue injury in a subject, comprising administering an effective amount of plasminogen to the subject to protect the renal tissues.
Item 10. The method of item 9, wherein the plasminogen alleviates apoptosis in a renal tissue caused by an acute renal tissue injury.
Item 11. The method of item 9 or 10, wherein the plasminogen promotes repair of an injured renal tissue.
Item 12. The method of any one of items 9 to 11, wherein the plasminogen alleviates fibrosis of the injured renal tissue.
Item 13. The method of any one of items 9 to 12, wherein the plasminogen promotes recovery of renal function.
Item 14. The method of any one of items 1 to 13, wherein the renal injury is acute glomerulonephritis, acute pyelonephritis, an acute renal injury, acute renal failure, acute renal insufficiency, and acute tubular necrosis.
Item 15. The method of items 1 to 13, wherein the acute renal injury is an acute renal injury induced by a chemotherapeutic drug.
In another aspect, the present invention relates to: Item 16. A method for preventing or treating a chronic renal tissue injury in a subject, comprising administering an effective amount of plasminogen to the subject to protect the renal tissues.
Item 17. The method of item 16, wherein the plasminogen alleviates apoptosis in a renal tissue.
Item 18. The method of item 16 or 17, wherein the plasminogen promotes repair of an injured renal tissue.
Item 19. The method of any one of items 16 to 18, wherein the plasminogen alleviates fibrosis of the injured renal tissue.
Item 20. The method of any one of items 16 to 19, wherein the plasminogen promotes recovery of renal function.
Item 21. The method of any one of items 16 to 20, wherein the chronic renal injury is a renal tissue injury caused by a chronic renal tissue disease.
Item 22. The method of any one of items 16 to 20, wherein the chronic renal injury is a renal tissue injury elicited or accompanied by other diseases.
Item 23. The method of item 22, wherein the other diseases comprise hypertension, diabetes mellitus, atherosclerosis, hyperlipemia, hepatitis, hepatic cirrhosis, coronary heart disease, angina pectoris, and myocardial infarction.
Item 24. The method of item 23, wherein the other diseases are hypertension, diabetes mellitus, atherosclerosis, and hyperlipemia.
In another aspect, the present invention relates to: Item 25. A method for preventing or treating a lipid deposition-induced renal tissue injury in a subject, comprising administering an effective amount of plasminogen to the subject.
Item 26. The method of item 25, wherein the lipid deposition is induced by hyperlipemia caused by abnormal fat or glucose metabolism in the subject.
In another aspect, the present invention relates to: Item 27. A method for preventing or treating a renal tissue injury elicited or accompanied by diabetes mellitus in a subject, comprising administering an effective amount of plasminogen to the subject.
In another aspect, the present invention relates to: Item 28. A method for preventing or treating a renal tissue injury elicited or accompanied by hyperlipemia in a subject, comprising administering an effective amount of plasminogen to the subject.
In another aspect, the present invention relates to: Item 29. A method for preventing or treating a renal tissue injury elicited or accompanied by atherosclerosis in a subject, comprising administering an effective amount of plasminogen to the subject.
In another aspect, the present invention relates to: Item 30. A method for preventing or treating an ischemic renal tissue injury in a subject, comprising administering an effective amount of plasminogen to the subject.
Item 31. The method of item 30, wherein the plasminogen alleviates apoptosis in a renal tissue.
Item 32. The method of item 30 or 31, wherein the plasminogen promotes repair of an injured renal tissue.
Item 33. The method of any one of items 30 to 32, wherein the plasminogen alleviates fibrosis of the injured renal tissue.
Item 34. The method of any one of items 30 to 33, wherein the plasminogen promotes recovery of renal function.
Item 35. The method of any one of items 30 to 34, wherein the ischemia is caused by stenosis of a vascular lumen.
Item 36. The method of any one of items 30 to 34, wherein the ischemia is caused by a thrombus blocking a blood vessel.
Item 37. The method of item 35 or 36, wherein the ischemia is caused by hypertension, diabetes mellitus, atherosclerosis, and a heart disease.
In another aspect, the present invention relates to: Item 38. A method for preventing or treating a renal tissue injury induced by ischemic reperfusion in a subject, comprising administering an effective amount of plasminogen to the subject.
In another aspect, the present invention relates to: Item 39. A method for preventing or treating a renal tissue injury induced by an autoimmune response in a subject, comprising administering an effective amount of plasminogen to the subject.
Item 40. The method of item 39, wherein the renal tissue injury induced by an autoimmune response is caused by systemic sclerosis.
In another aspect, the present invention relates to: Item 41. A method for preventing or treating an inflammation-induced renal tissue injury in a subject, comprising administering an effective amount of plasminogen to the subject.
Item 42. The method of item 41, wherein the inflammation is an acute and chronic renal parenchymal inflammation or renal interstitial inflammation.
Item 43. The method of item 42, wherein the plasminogen alleviates apoptosis in a renal tissue.
Item 44. The method of item 42 or 43, wherein the plasminogen promotes repair of an injured renal tissue.
Item 45. The method of any one of items 41 to 44, wherein the plasminogen alleviates fibrosis of the injured renal tissue.
Item 46. The method of any one of items 41 to 45, wherein the plasminogen promotes recovery of renal function.
Item 47. The method of any one of items 1 to 46, wherein the plasminogen has at least 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98% or 99% sequence identity with SEQ ID No. 2, 6, 8, 10 or 12, and still has the plasminogen activity.
Item 48. The method of any one of items 1 to 47, wherein the plasminogen is a protein that has 1-100, 1-90, 1-80, 1-70, 1-60, 1-50, 1-45, 1-40, 1-35, 1-30, 1-25, 1-20, 1-15, 1-10, 1-5, 1-4, 1-3, 1-2 or 1 amino acid added, deleted and/or substituted in SEQ ID No. 2, 6, 8, 10 or 12, and still has the plasminogen activity.
Item 49. The method of any one of items 1 to 48, wherein the plasminogen is a protein that comprises a plasminogen active fragment and still has the plasminogen activity.
Item 50. The method of any one of items 1 to 49, wherein the plasminogen is selected from Glu-plasminogen, Lys-plasminogen, mini-plasminogen, micro-plasminogen, delta-plasminogen or their variants that retain the plasminogen activity.
Item 51. The method of any one of items 1 to 50, wherein the plasminogen is administered in combination with one or more drugs selected from an antihypertensive drug, a hypolipidemic drug, an antibiotic drug, an anticoagulant drug, a thrombolytic drug, a diuretic drug, an anti-tumor drug, a hypoglycemic drug, a non-steroidal anti-inflammatory drug, an immunomodulatory drug, an anti-infective drug, an antiviral drug, a hormone, and an active ingredient of a natural product.
Item 52. The method of any one of items 1 to 51, wherein the plasminogen is a natural or synthetic human plasminogen, or a variant or fragment thereof that still retains the plasminogen activity.
Item 53. The method of any one of items 1 to 51, wherein the plasminogen is an ortholog of human plasminogen from a primate or a rodent, or a variant or fragment thereof that still retains the plasminogen activity.
Item 54. The method of any one of items 1 to 53, wherein the amino acids of the plasminogen are as shown in SEQ ID No. 2, 6, 8, 10 or 12.
Item 55. The method of any one of items 1 to 54, wherein the plasminogen is a natural human plasminogen.
Item 56. The method of any one of items 1 to 55, wherein the subject is a human.
Item 57. The method of any one of items 1 to 26, wherein the subject has a lack or deficiency of plasminogen.
Item 58. The method of item 57, wherein the lack or deficiency is congenital, secondary and/or local.
In another aspect, the present invention relates to: Item 59. A plasminogen for use in the method of any one of items 1 to 58.
In another aspect, the present invention relates to: Item 60. A pharmaceutical composition, comprising a pharmaceutically acceptable carrier and the plasminogen for use in the method of any one of items 1 to 58.
In another aspect, the present invention relates to: Item 61. A preventive or therapeutic kit comprising: (i) the plasminogen for use in the method of any one of items 1 to 58, and (ii) a means for delivering the plasminogen to the subject.
Item 62. The kit of item 61, wherein the means is a syringe or a vial.
Item 63. The kit of item 61 or 62, further comprising a label or an instruction for use indicating the administration of the plasminogen to the subject to implement the method of any one of items 1 to 58.
In another aspect, the present invention relates to: Item 64. An article of manufacture, comprising:
a container comprising a label; and
(i) the plasminogen for use in the method of any one of items 1 to 58 or a pharmaceutical composition comprising the plasminogen, wherein the label indicates the administration of the plasminogen or the composition to the subject to implement the method of any one of items 1 to 58.
Item 65. The kit of any one of items 61 to 63 or the article of manufacture of item 64, further comprising one or more additional means or containers containing other drugs.
Item 66. The kit or the article of manufacture of item 65, wherein the other drugs are selected from a group of: a hypolipidemic drug, an anti-platelet drug, an antihypertensive drug, a vasodilator, a hypoglycemic drug, an anticoagulant drug, a thrombolytic drug, a hepatoprotective drug, an anti-arrhythmia drug, a cardiotonic drug, a diuretic drug, an anti-infective drug, an antiviral drug, an immunomodulatory drug, an inflammatory regulatory drug, an anti-tumor drug, a hormone drug, and thyroxine.
The present invention further relates to the use of plasminogen for implementing the method of any one of items 1 to 58.
The present invention further relates to the use of plasminogen in the preparation of a medicament, a pharmaceutical composition, an article of manufacture, and a kit for the method of any one of items 1 to 58.
In some embodiments of the above-mentioned method, the plasminogen is administered by systemic or topical route, preferably by the following routes:
intravenous, intramuscular, and subcutaneous administration of plasminogen for treatment. In some embodiments of the above-mentioned method, the plasminogen is administered in combination with a suitable polypeptide carrier or stabilizer. In some embodiments of the above-mentioned method, the plasminogen is administered at a dosage of 0.0001-2000 mg/kg, 0.001-800 mg/kg, 0.01-600 mg/kg, 0.1-400 mg/kg, 1-200 mg/kg, 1-100 mg/kg or 10-100 mg/kg (by per kg of body weight) or 0.0001-2000 mg/cm2, 0.001-800 mg/cm2, 0.01-600 mg/cm2, 0.1-400 mg/cm2, 1-200 mg/cm2, 1-100 mg/cm2 or 10-100 mg/cm2 (by per square centimeter of body surface area) daily, preferably the dosage is repeated at least once, preferably the dosage is administered at least daily.
The present invention explicitly encompasses all the combinations of technical features belonging to the embodiments of the present invention, and these combined technical solutions have been explicitly disclosed in the present application, as if the above-mentioned technical solutions were individually and explicitly disclosed. In addition, the present invention also explicitly encompasses all the combinations between various embodiments and elements thereof, and the combined technical solutions are explicitly disclosed herein.
“Nephropathy” is renal structural changes and dysfunction caused by various causes.
“Plasmin” is a very important enzyme that exists in the blood and can hydrolyze fibrin clots into fibrin degradation products and D-dimers. “Plasminogen” is the zymogenic form of plasmin, and based on the sequence in the swiss prot and calculated from the amino acid sequence (SEQ ID No. 4) of the natural human plasminogen containing a signal peptide, is a glycoprotein composed of 810 amino acids, which has a molecular weight of about 92 kD and is synthesized mainly in the liver and capable of circulating in the blood; and the cDNA sequence encoding this amino acid sequence is as shown in SEQ ID No. 3. Full-length plasminogen contains seven domains: a C-terminal serine protease domain, an N-terminal Pan Apple (PAp) domain and five Kringle domains (Kringles 1-5). Referring to the sequence in the swiss prot, the signal peptide comprises residues Metl-Gly19, PAp comprises residues Glu20-Va198, Kringle 1 comprises residues Cys103-Cys181, Kringle 2 comprises residues Glu184-Cys262, Kringle 3 comprises residues Cys275-Cys352, Kringle 4 comprises residues Cys377-Cys454, and Kringle 5 comprises residues Cys481-Cys560. According to the NCBI data, the serine protease domain comprises residues Val581-Arg804.
Glu-plasminogen is a natural full-length plasminogen and is composed of 791 amino acids (without a signal peptide of 19 amino acids); the cDNA sequence encoding this sequence is as shown in SEQ ID No. 1; and the amino acid sequence is as shown in SEQ ID No. 2. In vivo, Lys-plasminogen, which is formed by hydrolysis of amino acids at positions 76-77 of Glu-plasminogen, is also present, as shown in SEQ ID No.6; and the cDNA sequence encoding this amino acid sequence is as shown in SEQ ID No.5. δ-plasminogen is a fragment of full-length plasminogen that lacks the structure of Kringle 2-Kringle 5 and contains only Kringle 1 and the serine protease domain[22, 23]. The amino acid sequence (SEQ ID No. 8) of δ-plasminogen has been reported in the literature[23], and the cDNA sequence encoding this amino acid sequence is as shown in SEQ ID No. 7. Mini-plasminogen is composed of Kringle 5 and the serine protease domain, and has been reported in the literature to comprise residues Val443-Asn791 (with the Glu residue of the Glu-plasminogen sequence that does not contain a signal peptide as the starting amino acid)[24]; the amino acid sequence is as shown in SEQ ID No. 10; and the cDNA sequence encoding this amino acid sequence is as shown in SEQ ID No. 9. Micro-plasminogen comprises only the serine protease domain, the amino acid sequence of which has been reported in the literature to comprise residues Ala543-Asn791 (with the Glu residue of the Glu-plasminogen sequence that does not contain a signal peptide as the starting amino acid)[25], and the sequence of which has been also reported in patent document CN 102154253 A to comprise residues Lys531-Asn791 (with the Glu residue of the Glu-plasminogen sequence that does not contain a signal peptide as the starting amino acid) (the sequence in this patent application refers to the patent document CN 102154253 A); the amino acid sequence is as shown in SEQ ID No. 12; and the cDNA sequence encoding this amino acid sequence is as shown in SEQ ID No. 11.
In the present invention, “plasmin” is used interchangeably with “fibrinolysin” and “fibrinoclase”, and the terms have the same meaning; and “plasminogen” is used interchangeably with “plasminogen” and “fibrinoclase zymogen”, and the terms have the same meaning.
In the present application, the meaning of “lack” in plasminogen is that the content or activity of plasminogen in the body of a subject is lower than that of a normal person, which is low enough to affect the normal physiological function of the subject; and the meaning of “deficiency” in plasminogen is that the content or activity of plasminogen in the body of a subject is significantly lower than that of a normal person, or even the activity or expression is extremely small, and only through exogenous supply can the normal physiological function be maintained.
Those skilled in the art can understand that all the technical solutions of the plasminogen of the present invention are suitable for plasmin. Therefore, the technical solutions described in the present invention cover plasminogen and plasmin.
In the course of circulation, plasminogen is in a closed, inactive conformation, but when bound to thrombi or cell surfaces, it is converted into an active plasmin in an open conformation under the mediation of a plasminogen activator (PA). The active plasmin can further hydrolyze the fibrin clots to fibrin degradation products and D-dimers, thereby dissolving the thrombi. The PAp domain of plasminogen comprises an important determinant that maintains plasminogen in an inactive, closed conformation, and the KR domain is capable of binding to lysine residues present on receptors and substrates. A variety of enzymes that can serve as plasminogen activators are known, including: tissue plasminogen activator (tPA), urokinase plasminogen activator (uPA), kallikrein, coagulation factor XII (Hagmann factor), and the like.
“Plasminogen active fragment” refers to an active fragment in the plasminogen protein that is capable of binding to a target sequence in a substrate and exerting the proteolytic function. The technical solutions of the present invention involving plasminogen encompass technical solutions in which plasminogen is replaced with a plasminogen active fragment. The plasminogen active fragment of the present invention is a protein comprising a serine protease domain of plasminogen. Preferably, the plasminogen active fragment of the present invention comprises SEQ ID No.14, or an amino acid sequence having an amino acid sequence identity of at least 80%, 90%, 95%, 96%, 97%, 98% or 99% with SEQ ID No.14. Therefore, plasminogen of the present invention comprises a protein containing the plasminogen active fragment and still having the plasminogen activity.
At present, methods for determining plasminogen and its activity in blood include: detection of tissue plasminogen activator activity (t-PAA), detection of tissue plasminogen activator antigen (t-PAAg) in plasma, detection of tissue plasminogen activity (plgA) in plasma, detection of tissue plasminogen antigen (plgAg) in plasma, detection of activity of the inhibitor of tissue plasminogen activators in plasma, detection of inhibitor antigens of tissue plasminogen activators in plasma and detection of plasmin-anti-plasmin (PAP) complex in plasma. The most commonly used detection method is the chromogenic substrate method: streptokinase (SK) and a chromogenic substrate are added to a test plasma, the plasminogen in the test plasma is converted into plasmin by the action of SK, the plasmin acts on the chromogenic substrate, and then it is determined that the increase in absorbance is directly proportional to plasminogen activity using a spectrophotometer. In addition, plasminogen activity in blood can also be determined by immunochemistry, gel electrophoresis, immunonephelometry, radioimmuno-diffusion and the like.
“Orthologues or orthologs” refer to homologs between different species, including both protein homologs and DNA homologs, and are also known as orthologous homologs and vertical homologs. The term specifically refers to proteins or genes that have evolved from the same ancestral gene in different species. The plasminogen of the present invention includes human natural plasminogen, and also includes orthologues or orthologs of plasminogens derived from different species and having plasminogen activity.
“Conservatively substituted variant” refers to one in which a given amino acid residue is changed without altering the overall conformation and function of the protein or enzyme, including, but not limited to, replacing an amino acid in the amino acid sequence of the parent protein by an amino acid with similar properties (such as acidity, alkalinity, hydrophobicity, etc.). Amino acids with similar properties are well known. For example, arginine, histidine and lysine are hydrophilic basic amino acids and are interchangeable. Similarly, isoleucine is a hydrophobic amino acid that can be replaced by leucine, methionine or valine. Therefore, the similarity of two proteins or amino acid sequences with similar functions may be different. For example, the similarity (identity) is 70%-99% based on the MEGALIGN algorithm. “Conservatively substituted variant” also includes a polypeptide or enzyme having amino acid identity of 60% or more, preferably 75% or more, more preferably 85% or more, even more preferably 90% or more as determined by the BLAST or FASTA algorithm, and having the same or substantially similar properties or functions as the natural or parent protein or enzyme.
“Isolated” plasminogen refers to the plasminogen protein that is isolated and/or recovered from its natural environment. In some embodiments, the plasminogen will be purified (1) to a purity of greater than 90%, greater than 95% or greater than 98% (by weight), as determined by the Lowry method, such as more than 99% (by weight); (2) to a degree sufficiently to obtain at least 15 residues of the N-terminal or internal amino acid sequence using a spinning cup sequenator; or (3) to homogeneity, which is determined by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) under reducing or non-reducing conditions using Coomassie blue or silver staining. Isolated plasminogen also includes plasminogen prepared from recombinant cells by bioengineering techniques and separated by at least one purification step.
The terms “polypeptide”, “peptide” and “protein” are used interchangeably herein and refer to polymeric forms of amino acids of any length, which may include genetically encoded and non-genetically encoded amino acids, chemically or biochemically modified or derivatized amino acids, and polypeptides having modified peptide backbones. The term includes fusion proteins, including, but not limited to, fusion proteins having heterologous amino acid sequences, fusions having heterologous and homologous leader sequences (with or without N-terminal methionine residues); and the like.
The “percent amino acid sequence identity (%)” with respect to the reference polypeptide sequence is defined as the percentage of amino acid residues in the candidate sequence identical to the amino acid residues in the reference polypeptide sequence when a gap is introduced as necessary to achieve maximal percent sequence identity and no conservative substitutions are considered as part of sequence identity. The comparison for purposes of determining percent amino acid sequence identity can be achieved in a variety of ways within the skill in the art, for example using publicly available computer softwares, such as BLAST, BLAST-2, ALIGN or Megalign (DNASTAR) software. Those skilled in the art can determine appropriate parameters for aligning sequences, including any algorithm needed to achieve the maximum comparison over the full length of the sequences being compared. However, for purposes of the present invention, the percent amino acid sequence identity value is generated using the sequence comparison computer program ALIGN-2.
In the case of comparing amino acid sequences using ALIGN-2, the % amino acid sequence identity of a given amino acid sequence A relative to a given amino acid sequence B (or may be expressed as a given amino acid sequence A having or containing a certain % amino acid sequence identity relative to, with or for a given amino acid sequence B) is calculated as follows:
fraction X/Y×100
wherein X is the number of identically matched amino acid residues scored by the sequence alignment program ALIGN-2 in the alignment of A and B using the program, and wherein Y is the total number of amino acid residues in B. It will be appreciated that where the length of amino acid sequence A is not equal to the length of amino acid sequence B, the % amino acid sequence identity of A relative to B will not be equal to the % amino acid sequence identity of B relative to A. Unless specifically stated otherwise, all the % amino acid sequence identity values used herein are obtained using the ALIGN-2 computer program as described in the previous paragraph.
As used herein, the terms “treatment” and “treating” refer to obtaining a desired pharmacological and/or physiologic effect. The effect may be complete or partial prevention of a disease or its symptoms and/or partial or complete cure of the disease and/or its symptoms, and includes: (a) prevention of the disease from developing in a subject that may have a predisposition to the disease but has not been diagnosed as having the disease; (b) suppression of the disease, i.e., blocking its formation; and (c) alleviation of the disease and/or its symptoms, i.e., eliminating the disease and/or its symptoms.
The terms “individual”, “subject” and “patient” are used interchangeably herein and refer to mammals, including, but not limited to, murine (rats and mice), non-human primates, humans, dogs, cats, hoofed animals (e.g., horses, cattle, sheep, pigs, goats) and so on.
“Therapeutically effective amount” or “effective amount” refers to an amount of plasminogen sufficient to achieve the prevention and/or treatment of a disease when administered to a mammal or another subject to treat the disease. The “therapeutically effective amount” will vary depending on the plasminogen used, the severity of the disease and/or its symptoms, as well as the age, body weight of the subject to be treated, and the like.
2. Preparation of the Plasminogen of the Present Invention
Plasminogen can be isolated and purified from nature for further therapeutic uses, and can also be synthesized by standard chemical peptide synthesis techniques. When chemically synthesized, a polypeptide can be subjected to liquid or solid phase synthesis. Solid phase polypeptide synthesis (SPPS) is a method suitable for chemical synthesis of plasminogen, in which the C-terminal amino acid of a sequence is attached to an insoluble support, followed by the sequential addition of the remaining amino acids in the sequence. Various forms of SPPS, such as Fmoc and Boc, can be used to synthesize plasminogen. Techniques for solid phase synthesis are described in Barany and Solid-Phase Peptide Synthesis; pp. 3-284 in The Peptides: Analysis, Synthesis, Biology. Vol. 2: Special Methods in Peptide Synthesis, Part A., Merrifield, et al. J. Am. Chem. Soc., 85: 2149-2156 (1963); Stewart et al. Solid Phase Peptide Synthesis, 2nd ed. Pierce Chem. Co., Rockford, Ill. (1984); and Ganesan A. 2006 Mini Rev. Med Chem. 6:3-10 and Camarero JA et al. 2005 Protein Pept Lett. 12:723-8. Briefly, small insoluble porous beads are treated with a functional unit on which a peptide chain is constructed. After repeated cycles of coupling/deprotection, the attached solid phase free N-terminal amine is coupled to a single N-protected amino acid unit. This unit is then deprotected to expose a new N-terminal amine that can be attached to another amino acid. The peptide remains immobilized on the solid phase before it is cut off.
Standard recombinant methods can be used to produce the plasminogen of the present invention. For example, a nucleic acid encoding plasminogen is inserted into an expression vector, so that it is operably linked to a regulatory sequence in the expression vector. Expression regulatory sequence includes, but is not limited to, promoters (e.g., naturally associated or heterologous promoters), signal sequences, enhancer elements and transcription termination sequences. Expression regulation can be a eukaryotic promoter system in a vector that is capable of transforming or transfecting eukaryotic host cells (e.g., COS or CHO cells). Once the vector is incorporated into a suitable host, the host is maintained under conditions suitable for high-level expression of the nucleotide sequence and collection and purification of plasminogen.
A suitable expression vector is usually replicated in a host organism as an episome or as an integral part of the host chromosomal DNA. In general, an expression vector contains a selective marker (e.g., ampicillin resistance, hygromycin resistance, tetracycline resistance, kanamycin resistance or neomycin resistance) to facilitate detection of those exogenous cells transformed with a desired DNA sequence.
Escherichia coli is an example of prokaryotic host cells that can be used to clone a polynucleotide encoding the subject antibody. Other microbial hosts suitable for use include Bacillus, for example, Bacillus subtilis and other species of Enterobacteriaceae (such as Salmonella spp. and Serratia spp.), and various Pseudomonas spp. In these prokaryotic hosts, expression vectors can also be generated which will typically contain an expression control sequence (e.g., origin of replication) that is compatible with the host cell. In addition, there will be many well-known promoters, such as the lactose promoter system, the tryptophan (trp) promoter system, the β-lactamase promoter system or the promoter system from phage lambda. Optionally in the case of manipulation of a gene sequence, a promoter will usually control expression, and has a ribosome binding site sequence and the like to initiate and complete transcription and translation.
Other microorganisms, such as yeast, can also be used for expression. Saccharomyces (e.g., S. cerevisiae) and Pichia are examples of suitable yeast host cells, in which a suitable vector has an expression control sequence (e.g., promoter), an origin of replication, a termination sequence and the like, as required. A typical promoter comprises 3-phosphoglycerate kinase and other glycolytic enzymes. Inducible yeast promoters specifically include promoters derived from alcohol dehydrogenase, isocytochrome C, and enzymes responsible for maltose and galactose utilization.
In addition to microorganisms, mammalian cells (e.g., mammalian cells cultured in cell culture in vitro) can also be used to express and generate the plasminogen of the present invention (e.g., a polynucleotide encoding a subject anti-Tau antibody). See Winnacker, From Genes to Clones, VCH Publishers, N.Y., N.Y. (1987). Suitable mammalian host cells include CHO cell lines, various Cos cell lines, HeLa cells, myeloma cell lines and transformed B cells or hybridomas. Expression vectors for these cells may comprise an expression control sequence, such as an origin of replication, promoter and enhancer (Queen et al. Immunol. Rev. 89:49 (1986)), as well as necessary processing information sites, such as a ribosome binding site, RNA splice site, polyadenylation site and transcription terminator sequence. Examples of suitable expression control sequences are promoters derived from white immunoglobulin gene, SV40, adenovirus, bovine papilloma virus, cytomegalovirus and the like. See Co et al. J. Immunol. 148:1149 (1992).
Once synthesized (chemically or recombinantly), the plasminogen of the present invention can be purified according to standard procedures in the art, including ammonium sulfate precipitation, affinity column, column chromatography, high performance liquid chromatography (HPLC), gel electrophoresis and the like. The plasminogen is substantially pure, e.g., at least about 80% to 85% pure, at least about 85% to 90% pure, at least about 90% to 95% pure, or 98% to 99% pure or purer, for example free of contaminants such as cell debris, macromolecules other than the subject antibody and the like.
3. Pharmaceutical Formulations
A therapeutic formulation can be prepared by mixing plasminogen of a desired purity with an optional pharmaceutical carrier, excipient or stabilizer (Remington's Pharmaceutical Sciences, 16th edition, Osol, A. ed. (1980)) to form a lyophilized preparation or an aqueous solution. Acceptable carriers, excipients and stabilizers are non-toxic to the recipient at the dosages and concentrations employed, and include buffers, such as phosphates, citrates and other organic acids; antioxidants, including ascorbic acid and methionine; preservatives (e.g., octadecyl dimethyl benzyl ammonium chloride; hexane chloride diamine; benzalkonium chloride and benzethonium chloride; phenol, butanol or benzyl alcohol; alkyl p-hydroxybenzoates, such as methyl or propyl p-hydroxybenzoate; catechol; resorcinol; cyclohexanol; 3-pentanol; and in-cresol); low molecular weight polypeptides (less than about 10 residues); proteins, such as serum albumin, gelatin or immunoglobulins; hydrophilic polymers, such as polyvinylpyrrolidone; amino acids, such as glycine, glutamine, asparagine, histidine, arginine or lysine; monosaccharides, disaccharides and other carbohydrates, including glucose, mannose or dextrins; chelating agents, such as EDTA; sugars, such as sucrose, mannitol, fucose or sorbitol; salt-forming counterions, such as sodium; metal complexes (e.g., zinc-protein complexes); and/or non-ionic surfactants, such as TWEEN™, PLURONICS™ or polyethylene glycol (PEG). Preferred lyophilized anti-VEGF antibody formulations are described in WO 97/04801, which is incorporated herein by reference.
The formulations of the invention may also comprise one or more active compounds required for the particular condition to be treated, preferably those that are complementary in activity and have no side effects with one another, for example anti-hypertensive drugs, anti-arrhythmic drugs, drugs for treating diabetes mellitus, and the like.
The plasminogen of the present invention may be encapsulated in microcapsules prepared by techniques such as coacervation or interfacial polymerization, for example, it may be incorporated in a colloid drug delivery system (e.g., liposomes, albumin microspheres, microemulsions, nanoparticles and nanocapsules), or incorporated in hydroxymethylcellulose or gel-microcapsules and poly-(methyl methacrylate) microcapsules in macroemulsions. These techniques are disclosed in Remington's Pharmaceutical Sciences, 16th edition, Osol, A. Ed. (1980).
The plasminogen of the present invention for in vivo administration must be sterile. This can be easily achieved by filtration through a sterile filtration membrane before or after freeze drying and reconstitution.
The plasminogen of the present invention can be prepared into a sustained-release preparation. Suitable examples of sustained-release preparations include solid hydrophobic polymer semi-permeable matrices having a shape and containing glycoproteins, such as films or microcapsules. Examples of sustained-release matrices include polyesters, hydrogels (e.g., poly(2-hydroxyethyl-methacrylate)) (Langer et al. J. Biomed. Mater. Res., 15:
167-277 (1981); and Langer, Chem. Tech., 12:98-105 (1982)), or poly(vinyl alcohol), polylactides (US Patent 3773919, and EP 58, 481), copolymer of L-glutamic acid and □ ethyl-L-glutamic acid (Sidman et al. Biopolymers 22:547(1983)), nondegradable ethylene-vinyl acetate (Langer et al. supra), or degradable lactic acid-glycolic acid copolymers such as Lupron Depot™ (injectable microspheres composed of lactic acid-glycolic acid copolymer and leuprolide acetate), and poly D-(−)-3-hydroxybutyric acid. Polymers, such as ethylene-vinyl acetate and lactic acid-glycolic acid, are able to persistently release molecules for 100 days or longer, while some hydrogels release proteins for a shorter period of time. A rational strategy for protein stabilization can be designed based on relevant mechanisms. For example, if the aggregation mechanism is discovered to be formation of an intermolecular S—S bond through thio-disulfide interchange, stability is achieved by modifying sulfhydryl residues, lyophilizing from acidic solutions, controlling moisture content, using appropriate additives, and developing specific polymer matrix compositions.
4. Administration and Dosage
The pharmaceutical composition of the present invention is administered in different ways, for example by intravenous, intraperitoneal, subcutaneous, intracranial, intrathecal, intraarterial (e.g., via carotid), intramuscular, intranasal, topical or intradermal administration or spinal cord or brain delivery. An aerosol preparation, such as a nasal spray preparation, comprises purified aqueous or other solutions of the active agent along with a preservative and isotonic agent. Such preparations are adjusted to a pH and isotonic state compatible with the nasal mucosa.
In some cases, the plasminogen pharmaceutical composition of the present invention may be modified or formulated in such a manner to provide its ability to cross the blood-brain barrier. Such plasminogen compositions is administered to an individual suffering from thrombosis and/or a thrombosis-related disease via a variety of enteral and parenteral routes of administration, including oral, intravenous and the like.
Preparations for parenteral administration include sterile aqueous or non-aqueous solutions, suspensions and emulsions. Examples of non-aqueous solvents are propylene glycol, polyethylene glycol, vegetable oils such as olive oil, and injectable organic esters such as ethyl oleate. Aqueous carriers include water, and alcoholic/aqueous solutions, emulsions or suspensions, including saline and buffered media. Parenteral vehicles include sodium chloride solution, Ringer's dextrose, dextrose and sodium chloride, or fixed oils. Intravenous vehicles include liquid and nutrient supplements, electrolyte supplements and the like. Preservatives and other additives may also be present, for example, such as antimicrobial agents, antioxidants, chelating agents and inert gases.
In some embodiments, the plasminogen of the invention is formulated with an agent that promotes the plasminogen to cross the blood-brain barrier. In some cases, the plasminogen of the present invention is fused directly or via a linker to a carrier molecule, peptide or protein that promotes the fusion to cross the blood brain barrier. In some embodiments, the plasminogen of the present invention is fused to a polypeptide that binds to an endogenous blood-brain barrier (BBB) receptor. The polypeptide that is linked to plasminogen and binds to an endogenous BBB receptor promotes the fusion to cross the BBB. Suitable polypeptides that bind to endogenous BBB receptors include antibodies (e.g., monoclonal antibodies) or antigen-binding fragments thereof that specifically bind to endogenous BBB receptors. Suitable endogenous BBB receptors include, but are not limited to, insulin receptors. In some cases, antibodies are encapsulated in liposomes. See, for example, US Patent Publication No. 2009/0156498.
The medical staff will determine the dosage regimen based on various clinical factors. As is well known in the medical field, the dosage of any patient depends on a variety of factors, including the patient's size, body surface area, age, the specific compound to be administered, sex, frequency and route of administration, overall health and other drugs administered simultaneously. The dosage range of the pharmaceutical composition comprising plasminogen of the present invention may be, for example, about 0.0001 to 2000 mg/kg, or about 0.001 to 500 mg/kg (such as 0.02 mg/kg, 0.25 mg/kg, 0.5 mg/kg, 0.75 mg/kg, 10 mg/kg and 50 mg/kg) of the subject's body weight daily. For example, the dosage may be 1 mg/kg body weight or 50 mg/kg body weight, or in the range of 1 mg/kg-50 mg/kg, or at least 1 mg/kg. Dosages above or below this exemplary range are also contemplated, especially considering the above factors. The intermediate dosages in the above range are also included in the scope of the present invention. A subject may be administered with such dosages daily, every other day, weekly or based on any other schedule determined by empirical analysis. An exemplary dosage schedule includes 1-10 mg/kg for consecutive days. During administration of the drug of the present invention, the therapeutic effect and safety of thrombosis and a thrombosis-related disease are required to be assessed real-timely and regularly.
5. Treatment Efficacy
One embodiment of the present invention relates to the judgment of treatment efficacy and treatment safety after treating a subject with plasminogen. Clinically, the methods for judging treatment efficacy include, but are not limited to, detection of the following indexes to assess renal function: serum creatinine level, creatinine clearance, 24-hour urinary protein excretion rate (UAER), glomerular filtration rate, urinary albumin/creatinine ratio, albumin secretion rate, renal biopsy, etc. For example, the glomerular filtration rate can indicate glomerular hyperfiltration and hyperperfusion, indicating the degree of relief of the early symptoms of diabetic nephropathy. The glomerular filtration rate is the volume of filtrate produced per minute by the kidneys and can be determined by a variety of methods, such as measurement of urinary clearance of filtration markers, such as glycans, iothalamates or iohexols. A more commonly used method can be estimating glomerular filtration rate by determining creatinine (a protein produced by muscle and released into the blood) clearance. The creatinine clearance (usually expressed in milliliters per minute) can be determined by comparing the level of creatinine collected in the urine with the level of creatinine in the blood over a given time (e.g., 12 or 24 hours). The typical creatinine clearance in adult males is approximately 97-137 ml/min, and that in adult females is approximately 88-128 ml/min. The creatinine clearance is directly proportional to urinary creatinine excretion and inversely proportional to serum creatinine concentration.
Creatinine clearance/glomerular filtration rate or urinary albumin excretion rate is usually used as the main efficacy assessment index. Furthermore, other secondary indexes can be added to assess the efficacy of the drug of the present invention on related complications, for example, detection of triglyceride, total cholesterol, low-density lipoprotein and the like is added to assess blood lipid changes; detection of systolic blood pressure and diastolic blood pressure before and after treatment is added to assess the degree of relief of hypertension; and so on.
6. Articles of Manufacture or Kits
One embodiment of the present invention relates to an article of manufacture or a kit comprising plasminogen of the present invention useful in the treatment of diabetic nephropathy. The article preferably includes a container, label or package insert. Suitable containers include bottles, vials, syringes and the like. The container can be made of various materials, such as glass or plastic. The container contains a composition that is effective to treat the disease or condition of the present invention and has a sterile access (for example, the container may be an intravenous solution bag or vial containing a plug that can be pierced by a hypodermic injection needle). At least one active agent in the composition is plasminogen. The label on or attached to the container indicates that the composition is used to treat the diabetic nephropathy of the present invention and diabetic nephropathy-related diseases. The article may further comprise a second container containing a pharmaceutically acceptable buffer, such as phosphate buffered saline, Ringer's solution and glucose solution. It may further comprise other substances required from a commercial and user perspective, including other buffers, diluents, filters, needles and syringes. In addition, the article comprises a package insert with instructions for use, including, for example, instructions to direct a user of the composition to administer to a patient the plasminogen composition and other drugs for treating an accompanying disease.
Ten healthy 8-9-week-old male C57 mice were randomly divided into two groups, five mice in each of the control group administered with vehicle PBS and the group administered with plasminogen. After the grouping was completed, a chemotherapy-induced injury model was established by single intraperitoneal injection of cisplatin at 10 mg/Kg body weight[33]. After the model was established, mice in the group administered with plasminogen were administered with plasminogen at a dose of 1 mg/0.1 mL/mouse/day via the tail vein, and an equal volume of PBS was administered to mice in the control group administered with vehicle PBS in the same manner. The day when the experiment began was Day 0, and the mice were weighed and grouped. The mice were injected with cisplatin intraperitoneally from day 1 for model establishment. Plasminogen or vehicle PBS was administered to the mice within 3 hours after completion of model establishment, and the administration period was 7 days. Mice were sacrificed on Day 8, and kidneys were fixed in 10% neutral formalin fixative for 24-48 hours. The fixed kidney tissues were paraffin-embedded after dehydration with alcohol gradient and permeabilization with xylene. The thickness of the tissue sections was 4 pm. The sections were dewaxed and rehydrated and washed with water once. The sections were repaired with citric acid for 30 minutes, and gently rinsed with water after cooling at room temperature for 10 minutes. The tissues were circled with a PAP pen, incubated with 3% hydrogen peroxide for 15 minutes, and washed with 0.01M PBS twice for 5 minutes each time. The sections were blocked with 5% normal goat serum (Vector laboratories, Inc., USA) for 30 minutes, and after the time was up, the goat serum liquid was discarded. Goat anti-mouse IgM (HRP) antibody (Abcam) was added to the sections dropwise, incubated for 1 hour at room temperature and washed with PBS twice for 5 minutes each time. The sections were developed with a DAB kit (Vector laboratories, Inc., USA). After washed with water three times, the sections were counterstained with hematoxylin for 30 seconds and flushed with running water for 5 minutes. After dehydration with a gradient, permeabilization and sealing, the sections were observed under an optical microscope at 200×.
IgM antibodies play an important role during the clearance of apoptotic and necrotic cells, and the local level of IgM antibodies at the injury site in tissues and organs are positively correlated with the degree of injury[29,30]. Therefore, detection of local level of IgM antibodies in tissues and organs can reflect the injury of the tissues and organs.
The results showed that the IgM-positive expression in the group administered with plasminogen (
Ten healthy 8-9-week-old male C57 mice were randomly divided into two groups, five mice in each of the control group administered with vehicle PBS and the group administered with plasminogen. After the grouping was completed, a chemotherapy-induced injury model was established by single intraperitoneal injection of cisplatin at 10 mg/Kg body weight[33]. After the model was established, mice in the group administered with plasminogen were administered with plasminogen at a dose of 1 mg/0 1 mL/mouse/day via tail vein injection, and an equal volume of PBS was administered to mice in the control group administered with vehicle PBS via tail vein injection. The day when the experiment began was Day 0, and the mice were weighed and grouped. The mice were injected with cisplatin intraperitoneally from day 1 for model establishment. Plasminogen or vehicle PBS was administered to the mice within 3 hours after completion of model establishment, and the administration period was 7 days. The mice were sacrificed on Day 8. The kidneys were fixed in 4% paraformaldehyde fixative for 24 hours. The fixed kidney tissues were paraffin-embedded after dehydration with alcohol gradient and permeabilization with xylene. The thickness of the tissue sections was 4 μm. The sections were dewaxed and rehydrated and washed with water once. The tissues were circled with a PAP pen, incubated with 3% hydrogen peroxide for 15 minutes, and washed with 0.01M PBS twice for 5 minutes each time. The sections were blocked with 5% normal goat serum (Vector laboratories, Inc., USA) for 30 minutes, and after the time was up, the goat serum liquid was discarded. Rabbit anti-mouse IV collagen antibody (Abcam) was added to the sections dropwise, incubated at 4° C. overnight, and washed with TBS twice for 5 minutes each time. The sections were incubated with a secondary antibody, goat anti-rabbit IgG (HRP) antibody (Abcam), for 1 hour at room temperature and washed with TBS twice for 5 minutes each time. The sections were developed with a DAB kit (Vector laboratories, Inc., USA). After washing with water three times, the sections were counterstained with hematoxylin for 30 seconds, returned to blue with running water for 5 minutes, and washed with TBS once. After dehydration with a gradient, permeabilization and sealing, the sections were observed under an optical microscope at 200×.
The results showed that the renal type IV collagen-positive expression in the control group administered with vehicle PBS (
Twenty 8- to 9-week-old PLG−/− mice and six PLG−/− mice were taken. PLG+/+ mice were randomly divided into two groups, 10 mice in each of the group administered with plasminogen and the control group administered with vehicle PBS. Mice in the group administered with plasminogen, the control group administered with vehicle PBS, and the PLG−/− group were fed with a 0.25% purine diet (Nantong TROPHIC) every day to establish the chronic renal injury model[26]. The day of model establishment was recorded as Day 1, and administration began at the same time. Mice in the group administered with plasminogen were administered with plasminogen at a dose of 1 mg/0.1 mL/mouse/day via the tail vein, and an equal volume of PBS was administered to mice in the control group administered with vehicle PBS in the same manner, both lasting for 10 consecutive days for model establishment. PLG−/− mice were not treated. The mice were sacrificed on Day 11. The kidneys were fixed in 4% paraformaldehyde for 24 hours. The fixed kidneys were paraffin-embedded after dehydration with alcohol gradient and permeabilization with xylene. The tissue sections were 3 μm thick. The sections were dewaxed and rehydrated, stained with hematoxylin and eosin (HE staining), differentiated with 1% hydrochloric acid in alcohol, and returned to blue with ammonia water. The sections were dehydrated with alcohol gradient, permeabilized with xylene, sealed with a neutral gum, and observed under an optical microscope at 200× (
The results showed that kidneys of PLG−/− mice (
Twelve 8- to 9-week-old male PLG+/+ mice and six PLG−/− mice were taken. PLG+/+ mice were randomly divided into two groups, 6 mice in each of the group administered with plasminogen and the control group administered with vehicle PBS. The modelling method for the chronic renal injury model was the same as described in Example 1. The day of model establishment was recorded as Day 1, and administration began at the same time. Mice in the group administered with plasminogen were administered with plasminogen at a dose of 1 mg/0.1 mL/mouse/day via the tail vein, and an equal volume of PBS was administered to mice in the control group administered with vehicle PBS in the same manner, both lasting for 10 consecutive days for model establishment. PLG−/− mice were not treated. The mice were sacrificed on Day 11. The kidneys were fixed in 4% paraformaldehyde for 24 hours. The fixed kidneys were paraffin-embedded after dehydration with alcohol gradient and permeabilization with xylene. The tissue sections was 3 μm thick. The sections were dewaxed and rehydrated and washed with water once. After stained with 0.1% Sirius red for 60 min, the sections were flushed with running water. After stained with hematoxylin for 1 min, the sections were flushed with running water, differentiated with 1% hydrochloric acid in alcohol and returned to blue with ammonia water, flushed with running water, dried and sealed. The sections were observed under an optical microscope at 200×.
Sirius red staining allows for long-lasting staining of collagen. As a special staining method for pathological sections, Sirius red staining can show the collagen tissue specifically.
The results showed that the collagen deposition in the group administered with plasminogen (
Eighteen 8- to 9-week-old male PLG+/+ mice were randomly divided into three groups, 6 mice in each of the blank control group, the group administered with plasminogen, and the control group administered with vehicle PBS. The modelling method for the chronic renal injury model was the same as described in Example 1. The day of model establishment was recorded as Day 1, and administration began at the same time. The blank control group was fed with a normal maintenance diet. Mice in the group administered with plasminogen were administered with plasminogen at a dose of 1 mg/0.1 mL/mouse/day via the tail vein, and an equal volume of PBS was administered to mice in the control group administered with vehicle PBS in the same manner, both lasting for 10 consecutive days for model establishment. Mice in the blank control group received no treatment. The day of model establishment and administration was recorded as Day 1. The mice were sacrificed on Day 11. The kidneys were fixed in 4% paraformaldehyde for 24 hours. The fixed kidneys were paraffin-embedded after dehydration with alcohol gradient and permeabilization with xylene. The thickness of the tissue sections was 3 μm. The sections were dewaxed and rehydrated and washed with water once. The tissues were circled with a PAP pen, incubated with 3% hydrogen peroxide for 15 minutes, and washed with 0.01M PBS twice for 5 minutes each time. The sections were blocked with 5% normal goat serum (Vector laboratories, Inc., USA) for 30 minutes, and after the time was up, the goat serum liquid was discarded. Rabbit anti-mouse Bcl-2 antibody (Abcam) was added to the sections dropwise, incubated at 4° C. overnight, and washed with 0.01 M PBS twice for 5 minutes each time. The sections were incubated with a secondary antibody, goat anti-rabbit IgG (HRP) antibody (Abcam), for 1 hour at room temperature and washed with 0.01 M PBS twice for 5 minutes each time. The sections were developed with a DAB kit (Vector laboratories, Inc., USA). After washed with water three times, the sections were counterstained with hematoxylin for 30 seconds and flushed with running water for 5 minutes. After dehydration with alcohol gradient, permeabilization with xylenehe, and sealing with a neutral gum, the sections were observed under an optical microscope at 200×.
Bcl-2 is an apoptosis inhibitory protein, and its expression will be down-regulated under the action of an apoptosis stimulating factor[27, 28]. The Bcl-2 immunohistochemical results showed that the renal Bcl-2-positive staining of the group administered with plasminogen (
Eighteen 8- to 9-week-old male PLG mice were randomly divided into three groups, 6 mice in each of the blank control group, the group administered with plasminogen, and the control group administered with vehicle PBS. The modelling method for the chronic renal injury model was the same as described in Example 1. The day of model establishment was recorded as Day 1, and administration began at the same time. The blank control group was fed with a normal maintenance diet. Mice in the group administered with plasminogen were administered with plasminogen at a dose of 1 mg/0.1 mL/mouse/day via the tail vein, and an equal volume of PBS was administered to mice in the control group administered with vehicle PBS in the same manner, both lasting for 10 consecutive days for model establishment. The blank control group received no treatment. The mice were sacrificed on Day 11. The kidneys were fixed in 4% paraformaldehyde for 24 hours. The fixed kidneys were paraffin-embedded after dehydration with alcohol gradient and permeabilization with xylene. The thickness of the tissue sections was 3 μm. The sections were dewaxed and rehydrated and washed with water once. The tissues were circled with a PAP pen, incubated with 3% hydrogen peroxide for 15 minutes, and washed with 0.01M PBS twice for 5 minutes each time. The sections were blocked with 5% normal goat serum (Vector laboratories, Inc., USA) for 30 minutes, and after the time was up, the goat serum liquid was discarded. Goat anti-mouse IgM (HRP) antibody (Abcam) was added to the sections dropwise, incubated for 1 hour at room temperature and washed with PBS twice for 5 minutes each time. The sections were developed with a DAB kit (Vector laboratories, Inc., USA). After washed with water three times, the sections were counterstained with hematoxylin for 30 seconds and flushed with running water for 5 minutes. After dehydration with a gradient, permeabilization and sealing, the sections were observed under an optical microscope at 200×.
IgM antibodies play an important role during the clearance of apoptotic and necrotic cells, and the local level of IgM antibodies in damaged tissues and organs is positively correlated with the degree of injury[29,30]. Therefore, detection of local level of IgM antibodies in tissues and organs can reflect the extent of injury of the tissues and organs.
The results showed that the renal IgM-positive staining of mice in the group administered with plasminogen (
Twelve 8- to 9-week-old male PLG mice and six PLG−/− mice were taken. PLG mice were randomly divided into two groups, 6 mice in each of the group administered with plasminogen and the control group administered with vehicle PBS. The modelling method for the chronic renal injury model was the same as described in Example 1. The day of model establishment was recorded as Day 1, and administration began at the same time. Both model establishment and administration lasted for a period of 4 days. The blank control group was fed with a normal maintenance diet. Mice in the group administered with plasminogen were administered with plasminogen at a dose of 1 mg/0 1 mL/mouse/day via the tail vein, and an equal volume of PBS was administered to mice in the control group administered with vehicle PBS in the same manner. PLG−/− mice received no treatment. The mice were sacrificed on Day 5. The kidneys were fixed in 4% paraformaldehyde for 24 hours. The fixed kidneys were paraffin-embedded after dehydration with alcohol gradient and permeabilization with xylene. The thickness of the tissue sections was 3 μm. The sections were dewaxed and rehydrated and washed with water once. The tissues were circled with a PAP pen, incubated with 3% hydrogen peroxide for 15 minutes, and washed with 0.01M PBS twice for 5 minutes each time. The sections were blocked with 5% normal goat serum (Vector laboratories, Inc., USA) for 30 minutes, and after the time was up, the goat serum liquid was discarded. Rabbit anti-mouse fibrin antibody (Abcam) was added to the sections dropwise, incubated at 4° C. overnight, and washed with PBS twice for 5 minutes each time. The sections were incubated with a secondary antibody, goat anti-rabbit IgG (HRP) antibody (Abcam), for 1 hour at room temperature and washed with PBS twice for 5 minutes each time. The sections were developed with a DAB kit (Vector laboratories, Inc., USA). After washed with water three times, the sections were counterstained with hematoxylin for 30 seconds and flushed with running water for 5 minutes. After dehydration with a gradient, permeabilization and sealing, the sections were observed under an optical microscope at 200×.
Fibrinogen is the precursor of fibrin, and in the presence of tissue injury, as a stress response to the body's injury, fibrinogen is hydrolyzed into fibrin and deposited at the injury site[31,32]. Therefore, the local fibrin level at the injury site can be used as a sign of the degree of injury.
The results showed that the renal fibrin-positive staining in the control group administered with vehicle PBS (
Ten 24- to 25-week-old male db/db mice were randomly divided into two groups, five in the control group administered with vehicle PBS and five in the group administered with plasminogen, respectively. The mice were weighed and grouped on the day when the experiment began, i.e. Day 0. Plasminogen or PBS was administered from day 1 for 31 consecutive days. Mice in the group administered with plasminogen were injected with plasminogen at a dose of 2 mg/0.2 mL/mouse/day via the tail vein, and an equal volume of PBS was administered to mice in the control group administered with vehicle PBS via the tail vein. The mice were sacrificed after administration of plasminogen for 31 days. The kidney tissues were fixed in 4% paraformaldehyde fixative for 24 hours. The fixed kidney tissues were paraffin-embedded after dehydration with alcohol gradient and permeabilization with xylene. The thickness of the tissue sections was 4 μm. The sections were dewaxed and rehydrated and washed with water once. The tissues were circled with a PAP pen, incubated with 3% hydrogen peroxide for 15 minutes, and washed with 0.01M PBS twice for 5 minutes each time. The sections were blocked with 5% normal goat serum (Vector laboratories, Inc., USA) for 30 minutes, and after the time was up, the goat serum liquid was discarded. Rabbit polyclonal antibody (Abcam) against IV collagen was added to the sections dropwise, incubated at 4° C. overnight, and washed with TBS twice for 5 minutes each time. The sections were incubated with a secondary antibody, goat anti-rabbit IgG (HRP) antibody (Abcam), for 1 hour at room temperature and washed with TBS twice. The sections were developed with a DAB kit (Vector laboratories, Inc., USA). After washed with water three times, the sections were counterstained with hematoxylin for 30 seconds and flushed with running water for 5 minutes. After gradient dehydration, permeabilization and sealing, the sections were observed under an optical microscope at 200×.
Diabetic nephropathy is a chronic complication of diabetes mellitus, and glomerular sclerosis and renal interstitial fibrosis are typical pathological changes[34]. The experimental results of the present invention showed that the positive staining of IV collagen in the group administered with plasminogen (
Ten 26-week-old male db/db mice were randomly divided into two groups, 5 mice in each of the control group administered with vehicle PBS and the group administered with plasminogen. The mice were weighed and grouped on the day when the experiment began, i.e. Day 0. Plasminogen or PBS was administered from day 1 for 35 consecutive days. Mice in the group administered with plasminogen were injected with plasminogen at a dose of 2 mg/0.2 mL/mouse/day via the tail vein, and an equal volume of PBS was administered to mice in the control group administered with vehicle PBS via the tail vein. The mice were sacrificed on Day 36. The kidney tissues were fixed in 4% paraformaldehyde fixative for 24 hours. The fixed kidney tissues were paraffin-embedded after dehydration with alcohol gradient and permeabilization with xylene. The thickness of the tissue sections was 4 μm. The sections were dewaxed and rehydrated and then put into a potassium dichromate solution overnight. The sections were stained with iron hematocylin for 3 to 5 minutes, and flushed with running water. The sections were differentiated with 1% hydrochloric acid in alcohol, treated with ammonia water for 1 second, and rinsed with water. The sections were stained in ponceau acid fuchsin fluid for 8 minutes, and rinsed rapidly in water. The sections were treated with 1% phosphomolybdic acid aqueous solution for about 2 minutes, and counterstained with aniline blue solution for 6 minutes. The sections were rinsed with 1% glacial acetic acid for about 1 minute. The sections were sealed after dehydration with absolute ethanol, and permeabilization with xylene, and were observed under an optical microscope at 200×.
Masson staining can reveal tissue fibrosis. The results showed that in the control group administered with vehicle PBS (
Ten 12-week-old male C57 mice were weighed and then randomly divided into two groups, 5 mice in each of the control group administered with vehicle PBS and the group administered with plasminogen. All mice were injected with bleomycin subcutaneously at a dose of 0.1 mg/0.1 mL/mouse/day to induce systemic sclerosis[35], and plasminogen or PBS was administered on the same day and this day was recorded as Day 1. The administration lasted for 21 consecutive days. Mice in the group administered with plasminogen were injected with plasminogen at a dose of 1 mg/0.1 mL/mouse/day via the tail vein, and an equal volume of PBS was administered to mice in the control group administered with vehicle PBS via the tail vein. The mice were sacrificed on Day 22. The kidneys were fixed in 4% paraformaldehyde fixative for 24 hours. The fixed kidneys were paraffin-embedded after dehydration with alcohol gradient and permeabilization with xylene. The tissue sections was 3 μm thick. The sections were dewaxed and rehydrated and washed with water once. After stained with 0.1% Sirius red in saturated picric acid for 30 min, the sections were flushed with running water for 2 min. After stained with hematoxylin for 1 min, the sections were flushed with running water, differentiated with 1% hydrochloric acid in alcohol, returned to blue with ammonia water, flushed with running water, dried and sealed with a neutral gum. The sections were observed under an optical microscope at 200×.
The results showed that in the bleomycin-induced systemic sclerosis mouse model, the collagen fibrosis in the kidney in the control group administered with vehicle PBS (
Ten 8- to 9-week-old PLG+/+ mice and six PLG−/− mice were taken. The modelling method for the chronic renal injury model was the same as described in Example 1. The day of model establishment was recorded as Day 1. The model establishment lasted for a period of 10 days. On Day 11, the blood was collected from removed eyeballs, and centrifuged to obtain a supernatant, which was detected for the concentration of urea nitrogen in the serum. The content of urea nitrogen was detected using a urea nitrogen detection kit (Nanjing Jiancheng Bioengineering Institute, Cat# C013-2) according to the method of the urea nitrogen detection kit.
The results showed that the concentration of urea nitrogen in sera in the PLG+/+ group was remarkably lower than that in the PLG−/− group, and the statistical difference was significant (
Twenty 8- to 9-week-old PLG+/+ mice and six PLG−/− mice were taken. PLG+/+ mice were randomly divided into two groups, 10 mice in each of the group administered with plasminogen and the control group administered with vehicle PBS. The modelling method for the chronic renal injury model was the same as described in Example 1. The day of model establishment was recorded as Day 1, and administration began at the same time, for an administration period of 4 days. Mice in the group administered with plasminogen were administered with plasminogen at a dose of 1 mg/0.1 mL/mouse/day via the tail vein, and an equal volume of PBS was administered to mice in the control group administered with vehicle PBS via the tail vein. PLG−/− mice received no treatment. On Day 5, the blood was collected from removed eyeballs, and centrifuged to obtain a supernatant, which was detected for the concentration of creatinine in the serum. The serum creatinine concentration was detected using a creatinine detection kit (Nanjing Jiancheng Bioengineering Institute, Cat# C011-2) according to the method of the detection kit.
The results showed that the concentration of creatinine in sera of mice in each of the control group administered with vehicle PBS and the group administered with plasminogen was remarkably lower than that in the PLG−/− group, and the statistical difference was significant. In addition, the concentration of creatinine in sera in the group administered with plasminogen was remarkably lower than that in the control group administered with vehicle PBS (
Nine 7-week-old male C57 mice were randomly divided into two groups, 5 mice in the group administered with plasminogen, and 4 mice in the control group administered with vehicle PBS. All mice received a single intraperitoneal injection of a folate (sigma A7876) solution at 250 mg/kg body weight to induce an acute renal injury[36]. Folate was dissolved in 0.3 mol/L NaHCO3. The day of model establishment was recorded as Day 1, and plasminogen or vehicle PBS was administered at the same time. Mice in the group administered with plasminogen were administered with plasminogen at a dose of 1 mg/0.1 mL/mouse/day via the tail vein, and an equal volume of PBS was administered to mice in the control group administered with vehicle PBS via the tail vein, both lasting for 7 days. On Day 8, the blood was collected from removed eyeballs, and centrifuged to obtain a supernatant, which was detected for the concentration of urea nitrogen in the serum. The content of urea nitrogen was detected using a urea nitrogen detection kit (Nanjing Jiancheng Bioengineering Institute, Cat# C013-2) according to the method of the urea nitrogen detection kit.
The results showed that the concentration of urea nitrogen in sera in the group administered with plasminogen was remarkably lower than that in the control group administered with vehicle PBS, and the statistical difference was nearly significant (P=0.06) (
Sixteen 9-week-old male C57 mice were fed with a 3% cholesterol high-fat diet (Nantong TROPHIC) for 4 weeks to induce hyperlipemia[37,38]. This model was designated as the 3% cholesterol hyperlipemia model. The model mice continued to be fed with the 3% cholesterol high-fat diet. Another five male C57 mice of the same week age were taken as the blank control group, and were fed with a normal maintenance diet during the experiment. 50 μL of blood was taken from each mouse three days before administration, and the total cholesterol was detected. The model mice were randomly divided into two groups based on the total cholesterol concentration and the body weight, i.e., the group administered with plasminogen, and the control group administered with vehicle PBS, 8 mice in each group. The first day of administration was recorded as Day 1. Mice in the group administered with plasminogen were injected with human plasminogen at a dose of 1 mg/0.1 mL/mouse/day via the tail vein, and an equal volume of PBS was administered to mice in the control group administered with vehicle PBS via the tail vein, both lasting for 30 days. The mice were sacrificed on Day 31. The kidneys were fixed in 4% paraformaldehyde for 24 to 48 hours, then sedimented in 15% and 30% sucrose at 4° C. overnight, respectively, and embedded in OCT. The frozen sections were 8 μm thick, stained with oil red O for 15 min, differentiated with 75% ethanol for 5 s, followed by nuclear staining with hematoxylin for 30 s, and sealing with glycerine and gelatin. The sections were observed under an optical microscope at 400×.
Oil red O staining can show lipid deposition and reflect the extent of lipid deposition[37]. The results showed that the fat deposition in kidney (indicated by arrow) of mice in the group administered with plasminogen (
Fifteen 7-week-old male C57 mice were randomly divided into three groups, 3 mice in the blank control group, 7 mice in the group administered with plasminogen, and 5 mice in the control group administered with vehicle PBS. Mice in the group administered with plasminogen and the control group administered with vehicle PBS received a single intraperitoneal injection of a folate (sigma A7876) solution at 250 mg/kg body weight to induce the acute renal injury model[36]. Mice in the blank control group received a single intraperitoneal injection of NaHCO3 solution of corresponding volume. Folate was dissolved in 0.3 mol/L NaHCO3 solution. The day of model establishment was recorded as Day 1, and plasminogen or vehicle PBS was administered at the same time. Mice in the group administered with plasminogen were administered with plasminogen at a dose of 1 mg/0.1 mL/mouse/day via the tail vein, and an equal volume of PBS was administered to mice in the control group administered with vehicle PBS via the tail vein, both lasting for 7 days. The mice were sacrificed on Day 8. The kidneys were fixed in 4% paraformaldehyde for 24 hours. The tissue sections were 3 μm thick. The sections were dewaxed and rehydrated, stained with hematoxylin and eosin (HE staining), differentiated with 1% hydrochloric acid in alcohol, and returned to blue with ammonia water. The sections were dehydrated with alcohol gradient, permeabilized with xylene, sealed with a neutral gum, and observed under an optical microscope at 200×.
The results showed that in the blank control group (
Twelve 7-week-old male C57 mice were randomly divided into two groups, 7 mice in the group administered with plasminogen, and 5 mice in the control group administered with vehicle PBS. All mice received a single intraperitoneal injection of a folate (sigma A7876) solution at 250 mg/kg body weight to induce an acute renal injury[36]. Folate was dissolved in 0.3 mol/L NaHCO3. The day of model establishment was recorded as Day 1, and plasminogen or vehicle PBS was administered at the same time. Mice in the group administered with plasminogen were administered with plasminogen at a dose of 1 mg/0.1 mL/mouse/day via the tail vein, and an equal volume of PBS was administered to mice in the control group administered with vehicle PBS via the tail vein, both lasting for 7 days. The mice were sacrificed on Day 8. The kidneys were fixed in 4% paraformaldehyde for 24 hours. The fixed kidneys were paraffin-embedded after dehydration with alcohol gradient and permeabilization with xylene. The thickness of the tissue sections was 3 μm. The sections were dewaxed and rehydrated and washed with water once. The tissues were circled with a PAP pen, incubated with 3% hydrogen peroxide for 15 minutes, and washed with 0.01M PBS twice for 5 minutes each time. The sections were blocked with 5% normal goat serum (Vector laboratories, Inc., USA) for 30 minutes, and after the time was up, the goat serum liquid was discarded. Rabbit anti-mouse Bcl-2 antibody (Abcam) was added to the sections dropwise, incubated at 4° C. overnight, and washed with 0.01 M PBS twice for 5 minutes each time. The sections were incubated with a secondary antibody, goat anti-rabbit IgG (HRP) antibody (Abcam), for 1 hour at room temperature and washed with 0.01 M PBS twice for 5 minutes each time. The sections were developed with a DAB kit (Vector laboratories, Inc., USA). After washed with water three times, the sections were counterstained with hematoxylin for 30 seconds and flushed with running water for 5 minutes. After dehydration with alcohol gradient, permeabilization with xylenehe, and sealing with a neutral gum, the sections were observed under an optical microscope at 200×.
The Bcl-2 immunohistochemical results showed that the renal Bcl-2-positive staining in the group administered with plasminogen (
Twelve 7-week-old male C57 mice were randomly divided into two groups, 7 mice in the group administered with plasminogen, and 5 mice in the control group administered with vehicle PBS. All mice received a single intraperitoneal injection of a folate (sigma A7876) solution at 250 mg/kg body weight to induce an acute renal injury[36]. Folate was dissolved in 0.3 mol/L NaHCO3 solution. The day of model establishment was recorded as Day 1, and plasminogen or vehicle PBS was administered at the same time. Mice in the group administered with plasminogen were administered with plasminogen at a dose of 1 mg/0.1 mL/mouse/day via the tail vein, and an equal volume of PBS was administered to mice in the control group administered with vehicle PBS via the tail vein, both lasting for 7 days. The mice were sacrificed on Day 8. The kidneys were fixed in 4% paraformaldehyde for 24 hours. The fixed kidneys were paraffin-embedded after dehydration with alcohol gradient and permeabilization with xylene. The thickness of the tissue sections was 3 μm. The sections were dewaxed and rehydrated and washed with water once. The tissues were circled with a PAP pen, incubated with 3% hydrogen peroxide for 15 minutes, and washed with 0.01M PBS twice for 5 minutes each time. The sections were blocked with 5% normal goat serum (Vector laboratories, Inc., USA) for 30 minutes, and after the time was up, the goat serum liquid was discarded. Goat anti-mouse IgM (HRP) antibody (Abcam) was added to the sections dropwise, incubated for 1 hour at room temperature and washed with PBS twice for 5 minutes each time. The sections were developed with a DAB kit (Vector laboratories, Inc., USA). After washed with water three times, the sections were counterstained with hematoxylin for 30 seconds and flushed with running water for 5 minutes. After dehydration with a gradient, permeabilization and sealing, the sections were observed under an optical microscope at 200×.
The results showed that the renal IgM-positive staining of mice in the group administered with plasminogen (
Sixteen 9-week-old male C57 mice were fed with a 3% cholesterol high-fat diet (Nantong TROPHIC) for 4 weeks to induce hyperlipemia[37,38]. This model was designated as the 3% cholesterol hyperlipemia model. The model mice continued to be fed with the 3% cholesterol high-fat diet. Another five male C57 mice of the same week age were taken as the blank control group, and were fed with a normal maintenance diet during the experiment. 50 μL of blood was taken from each mouse three days before administration, and the total cholesterol was detected. The model mice were randomly divided into two groups based on the total cholesterol concentration and the body weight, i.e., the group administered with plasminogen, and the control group administered with vehicle PBS, 8 mice in each group. The first day of administration was recorded as Day 1. Mice in the group administered with plasminogen were injected with human plasminogen at a dose of 1 mg/0.1 mL/mouse/day via the tail vein, and an equal volume of PBS was administered to mice in the control group administered with vehicle PBS via the tail vein. The mice were administered for 30 days. After the mice were administered on day 30, the mice were sacrificed on Day 31. The kidneys were fixed in 4% paraformaldehyde for 24 to 48 hours. The fixed tissues were paraffin-embedded after dehydration with alcohol gradient and permeabilization with xylene. The sections was 3 μm thick. The sections were dewaxed and rehydrated and washed with water once. After stained with 0.1% Sirius red in saturated picric acid for 30 min, the sections were flushed with running water for 2 min. After stained with hematoxylin for 1 min, the sections were flushed with running water, differentiated with 1% hydrochloric acid in alcohol, returned to blue with ammonia water, flushed with running water, dried and sealed with a neutral gum. The sections were observed under an optical microscope at 200×.
The results showed that the collagen deposition in kidney (indicated by arrow) in the group administered with plasminogen (
Nine 7- to 9-week-old male PLG+/+ mice were randomly divided into three groups, 3 mice in each of the sham operation group, the group administered with plasminogen, and the control group administered with vehicle PBS. All mice were anesthetized by intraperitoneal injection of pentobarbital sodium at 50 mg/kg body weight. Incisions were made in the abdomens of the mice in the group administered with plasminogen and the control group administered with vehicle PBS for the exposure of kidneys, bilateral arteries and veins were isolated and clamped by vascular clamps, then the kidney were moved back into the abdominal cavity, and the wound was closed for 45 min. After the time was up, the kidneys were exposed again, the vascular clamps were removed, the renal situations were observed, and the wounds were sutured after confirmation of reperfusion. In the sham operation group, an incisions was made in the abdomen for the exposure of the kidney only without ischemic treatment, and the wounds were sutured after the time was up[39]. After the operation was completed, each mouse received an intraperitoneal injection of 1 mL of normal saline at 37° C. The body temperature were kept at 36.5° C. to 38° C. during the operation. The day of model establishment was recorded as Day 1, and plasminogen or vehicle PBS was administered at the same time. Mice in the group administered with plasminogen were administered with plasminogen at a dose of 1 mg/0.1 mL/mouse/day via the tail vein, and an equal volume of PBS was administered to mice in the control group administered with vehicle PBS via the tail vein, both lasting for 7 days. Sham-operated mice received no injection treatment The mice were sacrificed on Day 8. The kidneys were fixed in 4% paraformaldehyde for 24 hours. The tissue sections were 3 μm thick. The sections were dewaxed and rehydrated, stained with hematoxylin and eosin (HE staining), differentiated with 1% hydrochloric acid in alcohol, and returned to blue with ammonia water. The sections were dehydrated with alcohol gradient, permeabilized with xylene, sealed with a neutral gum, and observed under an optical microscope at 200×.
The results showed that in the sham operation group (
[1] James L. Pirkle, MD1 and Barry I. Freedman, MD. Hypertension and chronic kidney disease: controversies in pathogenesis and treatment, Minerva UrolNefrol. 2013 March ; 65(1): 37-50.
[2] Nguyen D C A, Touyz R M. A new look at the renin-angiotensin system-focusing on the vascular system [J] . Peptides, 2011,32 (10) : 2141-2150.
[3] Kimoto E, Shoji T. Shinohara K, et al. Regional arterialstiffness inpatient with type 2 diabetes and chronic kidney disease [J]. J Am Soc Nephrol, 2006, 17(8):2245-2252.
[4] Mogensen C E, DamsgaardEm, Frland A, et al, Microalbuminuria in non-insulin depedent diabetes [J]. Clin Nephrol. 1992, 38(1):28-39.
[5] Choudhury D, Ahmed Z. Drug-associated renal dysfunction and injury [J]. Nat Clin PractNephrol, 2006, 2: 80-91.
[6] Colares V S, Oliveira R B, Abdulkader R C. Nephrotoxicity of vancomycin in patients with normal serum creatinine [J]. Nephrol Dial Transplant, 2006, 21: 3608.
[7] Izzedine H, Launay-Vacher V, Deray G. Antiviral drug-induced nephrotoxicity [J]. Am J Kidney Dis, 2005, 45: 804-817.
[8] Uwai Y, Ida H, Tsuji Y, et al. Renal transport of adefovir, cidofovir, and tenofovir by SLC22A family members (hOAT1, hOAT3, and hOCT2) [J]. Pharm Res, 2007, 24: 811-815.
[9] Servais H, Ortiz A, Devuyst O, et al. Renal cell apoptosis induced by nephrotoxic drugs: cellular and molecular mechanisms and potential approaches to modulation [J]. Apoptosis, 2008, 13: 11-32.
[10] Taguchi T, Nazneen A, Abid M R, et al. Cisplatin-associated nephrotoxicity and pathological events [J]. ContribNephrol, 2005, 148: 107-121.
[11] Harirforoosh S, Jamali F. Renal adverse effects of nonsteroidal anti-inflammatory drugs [J]. Expert Opin Drug Saf, 2009, 8: 669-681.
[12] Lincoln T. Toxicology: danger in the diet [J]. Nature, 2007,448: 148.
[13] Guitard J, Kamar N, Mouzin M, et al. Sulfadiazine-related obstructive urinary tract lithiasis: an unusual cause of acute renal failure after kidney transplantation [J]. Clin Nephrol, 2005, 63: 405-407.
[14] Boucher B J. Renal failure and rhabdomyolysis associated with sitagliptin and simvastatin use. But what about the amiodarone? [J]. Diabet Med, 2009, 26: 192-193.
[15] Hsu C Y, McCulloch C E, Fan D, et al. Community-based incidence of acute renal failure [J]. Kidney Int, 2007, 72(2): 208-212.
[16] Liangos O, Wald R, O'Bell J W, et al. Epidemiology and outcomes of acute renal failure in hospitalized patients: a national survey [J]. Clin J Am Soc Nephrol, 2006, 1(1): 43-51.
[17] Hoste E A, Clermont G, Kersten A, et al. RIFLE criteria for acute kidney injury are associated with hospital mortality in critically ill patients: a cohort analysis [J]. Crit Care, 2006, 10(3): R73.
[18] Zhang L, Yang Y Y, Fu P. The development and problems of continuous renal replacement therapy [J]. Chin J Pract Inter Med, 2011, 31(4):301-304. [19] RENAL Replacement Therapy Study Investigators, Bellomo R, Cass A, et al. Intensity of continuous renal-replacement therapy in critically ill patients [J]. N Engl J Med, 2009, 361(17): 1627-1638.
[20] VA/NIH Acute Renal Failure Trial Network, Palevsky P M, Zhang J H, et al. Intensity of renal support in critically ill patients with acute kidney injury [J]. N Engl J Med, 2008, 359(1): 7-20.
[21] Coca S G, Yusuf B, Shlipak M G, et al. Long-term risk of mortality and other adverse outcomes after acute kidney injury: a systematic review and meta-analysis [J]. Am J Kidney Dis, 2009, 53(6): 961-973.
[22] Marder V J, Novokhatny V. Direct fibrinolytic agents: biochemical attributes, preclinical foundation and clinical potential [J]. Journal of Thrombosis and Haemostasis, 2010, 8(3): 433-444.
[23] Hunt J A, Petteway Jr S R, Scuderi P, et al. Simplified recombinant plasmin: production and functional comparison of a novel thrombolytic molecule with plasma-derived plasmin [J]. ThrombHaemost, 2008, 100(3): 413-419.
[24]Sottrup-Jensen L, Claeys H, Zajdel M, et al. The primary structure of human plasminogen: Isolation of two lysine-binding fragments and one “mini”-plasminogen (MW, 38,000) by elastase-catalyzed-specific limited proteolysis [J]. Progress in chemical fibrinolysis and thrombolysis, 1978, 3: 191-209.
[25]Nagai N, Demarsin E, Van Hoef B, et al. Recombinant human microplasmin: production and potential therapeutic properties [J]. Journal of Thrombosis and Haemostasis, 2003, 1(2): 307-313.
[26] CristhianeFaveroAguiar,CristianeNaffah-de-Souza, Angela Castoldi et al. Administration of α-Galactosylceramide Improves Adenine-Induced Renal Injury. Mol Med. 2015 Jun. 18;21:553-62.
[27] Moungjaroen J, Nimmannit U, Callery P S, Wang L, Azad N, Lipipun V, Chanvorachote P, Rojanasakul Y (2006). Reactive oxygen species mediate caspase activation and apoptosis induced by lipoic acid in human lung epithelial cancer cells through Bcl-2 downregulation. J Pharmacol Exp Ther 319, 1062-1069.
[28] Wang L, Chanvorachote P, Toledo D, Stehlik C, Mercer R R, Castranova V, Rojanasakul Y (2008). Peroxide is a key mediator of Bcl-2 down-regulation and apoptosis induction by cisplatinin human lung cancer cells. Mol Pharmacol 73, 119-127.
[29] Zhang M, Takahashi K, Alicot E M, Vorup-Jensen T, Kessler B, et al. (2006) Activation of the lectin pathway by natural IgM in a model of ischemia/reperfusion injury. J Immunol 177: 4727-4734.
[30] Kim S J, Gershov D, Ma X, Brot N, Elkon K B (2002) I-PLA2 Activation during Apoptosis Promotes the Exposure of Membrane LysophosphatidylcholineLeading to Binding by Natural Immunoglobulin M Antibodies and Complement Activation. The Journal of Experimental Medicine 196: 655-665.
[31] Dimitrios Davalos, Katerina Akassoglou. Fibrinogen as a key regulator of inflammation in disease. Seminars in Immunopathology, 2012. 34(1):43-62.
[32] Valvi D, Mannino D M, Mullerova H, et al.Fibrinogen, chronic obstructive pulmonary disease (COPD) and outcomes in two United States cohorts. Int J Chron Obstruct Pulmon Dis 2012;7:173-82.
[33] Blanca Humanes, AlbertoLazaro, Sonia Camano et al. Cilastatin protects against cisplatin-induced nephrotoxicity without compromising its anticancer efficiency in rats. Kidney Int. 2012 September;82(6):652-63.
[34] Donnelly S M, Zhou X P, Hu ang J T et al. Prevention of early glomerulopathy with tolrestat in the streptozotocin-induced diabetic rat. Biochem Cell Biol. 1996;74(3):355-62.
[35] Yosuke Kanno, En Shu, Hiroyuki Kanoh and Mariko Seishima. The Antifibrotic Effect of a2AP Neutralization in Systemic Sclerosis Dermal Fibroblasts and Mouse Models of Systemic Sclerosis. Journal of Investigative Dermatology (2016) 136, 762e769
[36] Szczypka M S, Westover A J, Clouthier S G et al. Rare incorporation of bone marrow-derived cells into kidney after folic acid-induced injury. Stem Cells. 2005;23(1):44-54.
[37] Dominika Nackiewicz, Paromita Dey, Barbara Szczerba et al Inhibitor of differentiation 3, a transcription factor regulates hyperlipidemia associated kidney disease. Nephron Exp Nephrol. 2014; 126(3): 141-147.
[38] Ming Gul, Yu Zhang., Shengjie Fan et al. Extracts of RhizomaPolygonatiOdorati Prevent High-Fat Diet-Induced Metabolic Disorders in C57BL/6 Mice. PLoS ONE 8(11): e81724.
[39] Li Yang, Craig R. Brooks,Sheng Xiao et al. KIM-1-mediated phagocytosis reduces acute injuryto the kidney. J Clin Invest. 2015 April;125(4):1620-36.
| Number | Date | Country | Kind |
|---|---|---|---|
| PCT/CN2016/110169 | Dec 2016 | CN | national |
| PCT/CN2016/110174 | Dec 2016 | CN | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CN2017/089059 | 6/19/2017 | WO | 00 |
