US2014314712A1PendingUtilityA1

Fusion protein comprising an interleukin 4 and interleukin

Assignee: UMC UTRECHT HOLDING BVPriority: Nov 8, 2011Filed: Nov 8, 2012Published: Oct 23, 2014
Est. expiryNov 8, 2031(~5.3 yrs left)· nominal 20-yr term from priority
A61K 9/08A61K 9/0029A61K 38/2066A61K 9/0095A61K 45/06A61K 38/2026A61P 9/10A61P 9/14A61P 3/10A61P 37/00A61P 9/00A61P 37/08A61P 43/00A61P 7/08A61P 37/06A61P 37/02A61P 7/00A61P 37/04A61P 35/02A61P 29/00A61P 25/04A61P 31/04A61P 35/00C07K 14/5428C07K 2319/00A61K 38/00A61P 19/08A61P 19/02A61P 13/12C07K 14/5406A61P 11/00A61P 17/00A61P 19/06A61P 25/00A61P 1/04A61P 1/00A61P 17/06A61P 17/02
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Claims

Abstract

The invention is concerned with a fusion protein comprising interleukin 10 and interleukin 4, a nucleic acid molecule encoding such fusion protein, a vector comprising such nucleic acid molecule, and a host cell comprising such nucleic acid molecule or such vector. The invention further pertains to a method for producing such fusion protein. The fusion protein or a gene therapy vector encoding the fusion protein may be used in the prevention or treatment of osteoarthritis, chronic pain, a condition characterized by local or systemic inflammation, immune activation, and/or lymphoproliferation.

Claims

exact text as granted — not AI-modified
1 . A fusion protein comprising an interleukin 4 and interleukin 10. 
     
     
         2 . A fusion protein according to  claim 1 , wherein said interleukin 4 and said interleukin 10 are linked by a linker sequence. 
     
     
         3 . A fusion protein according to any one of  claims 1  or  2 , wherein the interleukin 4 is fused N-terminal of the interleukin 10. 
     
     
         4 . A fusion protein according to any one of  claims 1  or  2 , wherein the interleukin 10 is fused N-terminal of the interleukin 4. 
     
     
         5 . A fusion protein according to  claim 1 , which further comprises one or more chemical modifications. 
     
     
         6 . A fusion protein according to  claim 5 , wherein the chemical modification is selected from the group consisting of glycosylation, fucosylation, sialylation, and pegylation. 
     
     
         7 . A fusion protein according to  claim 1 , wherein said interleukin 10 is human interleukin 10. 
     
     
         8 . A fusion protein according to  claim 1 , wherein said interleukin 4 is human interleukin 4. 
     
     
         9 . A nucleic acid molecule comprising a polynucleotide encoding the fusion protein according to  claim 1 . 
     
     
         10 . A vector comprising the nucleic acid molecule of  claim 9 . 
     
     
         11 . A host cell comprising the nucleic acid molecule according to  claim 9  or the vector according to  claim 10 . 
     
     
         12 . A method for producing a fusion protein comprising an interleukin 4 and interleukin 10, said method comprising the steps of:
 culturing a host cell according to  claim 11  under conditions permitting the production of the fusion protein;   optionally, recovering the fusion protein.   
     
     
         13 . A pharmaceutical composition comprising the fusion protein according to  claim 1 , and a pharmaceutically acceptable carrier. 
     
     
         14 . A fusion protein according to  claim 1  for use as a medicament. 
     
     
         15 . A fusion protein according to  claim 1  for use in the prevention or treatment of osteoarthritis, chronic pain, a condition characterized by local or systemic inflammation, immune activation, and/or lymphoproliferation. 
     
     
         16 . A fusion protein for use according to  claim 14 , wherein said condition characterized by local or systemic inflammation, immune activation, lymphoproliferation and/or chronic pain is selected from the group consisting of: sepsis, adult respiratory distress syndrome, allo- and xenotransplantation, dermatitis, inflammatory bowel disease, sarcoidosis, allergies, psoriasis, ankylosing spondylarthitis, autoimmune diseases such as systemic lupus erythematosus and rheumatoid arthritis, glomerolonephritis, immune complex-induced and other forms of vasculitis, multiple sclerosis, Sjogren's disease, gout, lymphoproliferative diseases such as non Hodgkin lymphoma and B cell chronic lymphocytic leukemia, burn injuries, multiple trauma, stroke, myocardial infarction, atherosclerosis, diabetes mellitus, extracorporeal dialysis and blood oxygenation, ischemia-reperfusion injuries, toxicity induced by the in vivo administration of cytokines or therapeutic monoclonal antibodies, chronic pain syndrome and neuropathic and/or inflammatory pain. 
     
     
         17 . A fusion protein according to  claim 1  for use in the prevention or treatment of a clinical condition in a mammal, such as a human, for which interleukin 10 is indicated. 
     
     
         18 . A fusion protein according to  claim 1  for use in the prevention or treatment of a clinical condition in a mammal, such as a human, for which interleukin 4 is indicated. 
     
     
         19 . A gene therapy vector according to  claim 10  for use in the prevention or treatment of osteoarthritis, chronic pain, a condition characterized by local or systemic inflammation, immune activation, and/or lymphoproliferation. 
     
     
         20 . A vector for use according to  claim 19 , wherein said condition characterized by local or systemic inflammation, immune activation, and/or lymphoproliferation is selected from the group consisting of: sepsis, adult respiratory distress syndrome, allo- and xenotransplantation, dermatitis, inflammatory bowel disease, sarcoidosis, allergies, psoriasis, ankylosing spondylarthitis, autoimmune diseases such as systemic lupus erythematosus and rheumatoid arthritis, glomerolonephritis, immune complex-induced and other forms of vasculitis, multiple sclerosis, Sjogren's disease, gout, lymphoproliferatieve diseases such as non Hodgkin lymphoma and B cell chronic lymphocytic leukemia, burn injuries, multiple trauma, stroke, myocardial infarction, atherosclerosis, diabetes mellitus, extracorporeal dialysis and blood oxygenation, ischemia-reperfusion injuries, toxicity induced by the in vivo administration of cytokines or therapeutic monoclonal antibodies, chronic pain syndrome, and neuropathic and/or inflammatory pain.

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