Multiprotein-engineered cells secreting a multispecific antibody
US-2024344030-A1 · Oct 17, 2024 · US
US9694035B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9694035-B2 |
| Application number | US-201414334128-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 17, 2014 |
| Priority date | Mar 22, 2004 |
| Publication date | Jul 4, 2017 |
| Grant date | Jul 4, 2017 |
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Methods of treating autoimmune diseases, allergic responses, cancer, or inflammatory diseases in an animal, promoting wound healing, repairing epithelial damage and promoting angiogenesis in an organ or tissue of an animal by administering to the animal mesenchymal stem cells in an effective amount.
Opening claim text (preview).
The invention claimed is: 1. A method of reducing inflammation in the gastrointestinal tract of a patient in need thereof, comprising the step of intravenously or intraarterially administering to a human suffering from inflammation of the gastrointestinal tract a suspension of cells in an amount effective to reduce the inflammation, wherein the cells are genetically unmodified allogeneic mesenchymal stem cells, wherein the suspension of mesenchymal stem cells is at least 95% homogeneous and wherein the mesenchymal stem cells express CD73 and CD105. 2. The method of claim 1 , wherein the patient suffers from Crohn's disease, inflammatory bowel disease, gastrointestinal graft-versus-host disease (GVHD), or autoimmune gastritis. 3. The method of claim 2 , wherein the patient suffers from gastrointestinal graft-versus-host disease. 4. The method of claim 3 , wherein the patient was refractory to one or more treatments to GVHD. 5. The method of claim 1 , wherein the suspension further comprises an acceptable pharmaceutical carrier. 6. The method of claim 5 , wherein the acceptable pharmaceutical carrier is a pharmaceutically acceptable liquid medium for injection. 7. The method of claim 1 , wherein the suspension is administered in an amount of from about 1×10 5 cells/kg to about 1×10 7 cells/kg. 8. The method of claim 1 , wherein the suspension is administered in an amount of from about 1×10 6 cells/kg to about 5×10 6 cells/kg. 9. The method of claim 1 , wherein the suspension is administered in an amount of about 3×10 6 cells/kg. 10. The method of claim 1 , wherein the method comprises increasing production or secretion of an anti-inflammatory cytokines interleukin-4 or interleukin-10. 11. The method of claim 1 , wherein the method comprises reducing production or secretion of a pro-inflammatory cytokine in a human in need thereof. 12. The method of claim 2 , wherein the patient suffers from inflammatory bowel disease. 13. The method of claim 11 , wherein the pro-inflammatory cytokine that is reduced in production or secretion is selected from the group consisting of interferon-γ, TNF-α, and IL-17.
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