Claims for Patent: 7,955,809

Summary for Patent: 7,955,809

Title:	Method for measuring human megalin
Abstract:	This invention provides a method for measuring human megalin that can be performed in a simpler manner within a shorter period of time than is possible with conventional techniques, and that can also quantify human megalin. This invention also provides a method that enables diagnosis of functional diseases, which are specific to cells, tissues, or organs, in a site-directed manner at an early stage. Measurement of human megalin enables detection of a disease in an organ in which megalin expression is observed.
Inventor(s):	Ogasawara; Shinya (Niigata, JP), Miura; Shuhei (Niigata, JP), Saito; Akihiko (Niigata, JP), Takeda; Tetsuro (Niigata, JP)
Assignee:	Niigata University (Niigata, JP) Denka Seiken Co., Ltd. (Tokyo, JP)
Application Number:	12/293,992
Patent Claims:	1. A method for detecting a renal disease in which megalin expression is observed by measuring human megalin in a urine sample, comprising: (i) allowing the sample to react with a first ligand that is capable of binding to human megalin and that is bound to a solid support, (ii) allowing the sample to react with the second ligand, wherein the second ligand is capable of binding to human megalin, and then (iii) measuring the level of human megalin in the sample by measuring the amount of the complex formed between the first ligand, the human megalin and the second ligand, wherein an increased level of human megalin indicates a renal disease that is selected from the group consisting of nephritis, tubular renal disorder, and nephropathy. 2. The method according to claim wherein step (i) and step (ii) are carried out sequentially. 3. The method according to claim 1, wherein step (i) and step (ii) are carried out concurrently. 4. The method according to claim 1, wherein the first ligand and the second ligand are both antibodies. 5. The method according to claim 1, wherein the first ligand is lectin, which is specific to a sugar chain of human megalin, and the second ligand is an antibody. 6. The method according to claim 1, wherein the first ligand is an antibody and the second ligand is lectin, which is specific to a sugar chain of human megalin. 7. The method according to claim 1, wherein the first ligand is selected from the group consisting of: vitamin-binding protein, which is transcobalamin-vitamin B.sub.12, vitamin-D-binding protein, or retinol-binding protein; lipoprotein, which is apolipoprotein B, apolipoprotein E, apolipoprotein J/clusterin, or apolipoprotein H; hormone, which is parathyroid hormone (PTH), insulin, epithelial growth factor (EGF), prolactin, leptin, or thyroglobulin, a receptor of any thereof, or a receptor of such hormone; immune or stress response-associated protein, which is immunoglobulin light chain, purple acid phosphatase 1 (PAP-1), or .beta..sub.2-microglobulin; enzyme, which is plasminogen activator inhibitor-I (PAI-I), plasminogen activator inhibitor-I-urokinase (PAI-I-urokinase), plasminogen activator inhibitor-I-tissue plasminogen activator (PAI-I-tPA), prourokinase, lipoprotein lipase, plasminogen, .alpha.-amylase, .beta.-amylase, .alpha..sub.1-microglobulin, or lysozyme, an inhibitor of any thereof, or an inhibitor of such enzyme; drug or toxin, which is aminoglycoside, polymyxin aprotinin, or trichosantin; carrier protein, which is albumin, lactoferrin, hemoglobin, odorant-binding protein, transthyretin, or liver type fatty acid binding proteins (L-FABP); and receptor-associated protein (RAP), which is cytochrome-c, calcium (Ca.sup.2+), advanced glycation end products (AGE), cubilin, or Na.sup.+--H.sup.+ exchanger isoform 3 (NHE3) or binding fragment of such substance, and the second ligand is an antibody. 8. The method according to claim 1, wherein the first ligand is an antibody and the second ligand is selected from the group consisting of vitamin-binding protein, which is transcobalamin-vitamin B.sub.12, vitamin-D-binding protein, or retinol-binding protein; lipoprotein, which is apolipoprotein B, apolipoprotein E, apolipoprotein J/clusterin, or apolipoprotein H; hormone, which is parathyroid hormone (PTH), insulin, epithelial growth factor (EGF), prolactin, leptin, or thyroglobulin, a receptor of any thereof, or a receptor of such hormone; immune or stress response-associated protein, which is immunoglobulin light chain, purple acid phosphatase 1 (PAP-1), or .beta..sub.2-microglobulin; enzyme, which is plasminogen activator inhibitor-I (PAI-I), plasminogen activator inhibitor-I-urokinase (PAI-I-urokinase), plasminogen activator inhibitor-I-tissue plasminogen activator (PAI-I-tPA), prourokinase, lipoprotein lipase, plasminogen, .alpha.-amylase, .beta.-amylase, .alpha..sub.1-microglobulin, or lysozyme, an inhibitor of any thereof, or an inhibitor of such enzyme; drug or toxin, which is aminoglycoside, polymyxin B, aprotinin, or trichosantin; carrier protein, which is albumin, lactoferrin, hemoglobin, odorant-binding protein, transthyretin, or liver type fatty acid binding proteins (L-FABP); and receptor-associated protein (RAP), which is cytochrome-c, calcium (Ca.sup.2+), advanced glycation end products (AGE), cubilin, or Na.sup.+--H.sup.+ exchanger isoform 3 (NHE3) or binding fragment of such substance. 9. The method according to claim 1, wherein said renal disease is nephritis. 10. The method according to claim 1, wherein said renal disease is nephropathy. 11. The method according to claim 1, wherein said renal disease is renal tubular disorder.

Details for Patent 7,955,809

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Bayer Healthcare Pharmaceuticals Inc.	TRASYLOL	aprotinin	Injection	020304	12/29/1993		2026-03-28
Microbix Biosystems Inc.	KINLYTIC	urokinase	For Injection	021846	01/16/1978		2026-03-28
Nps Pharmaceuticals, Inc.	NATPARA	parathyroid hormone	For Injection	125511	01/23/2015		2026-03-28