US2022064600A1PendingUtilityA1

Methods of expanding myeloid cell populations and uses thereof

75
Assignee: CELLERANT THERAPEUTICS INCPriority: Oct 25, 2004Filed: Oct 12, 2021Published: Mar 3, 2022
Est. expiryOct 25, 2024(expired)· nominal 20-yr term from priority
A61K 40/50A61K 40/44A61K 40/10A61K 2239/38C12N 2501/2303C12N 5/0647C12N 2501/727C12N 2501/23A61K 2035/124A61K 9/10A61K 35/12A61P 31/12A61K 9/0014C12N 2501/22C12N 2500/99C12N 2501/125C12N 2500/90C12N 2501/145A61P 7/00C12N 2500/44A61P 31/04A61K 35/28A61P 31/10A61P 7/04A61P 7/06Y02A90/10C12N 2501/26A61P 5/00A61P 43/00A61K 35/15
75
PatentIndex Score
0
Cited by
0
References
0
Claims

Abstract

The present disclosure relates to a method of expanding myeloid progenitor cells by culturing an initial population of cells in a medium comprising a mixture of cytokines and growth factors that promote growth and expansion of the myeloid progenitor cells. The expanded cell population provides a source of cells as therapeutic treatments for neutropenia and/or thrombocytopenia arising in patients subjected to myeloablative therapy and hematopoietic stem cell transplantation.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method of improving impaired hematopoiesis in a human, comprising,
 administering to the human a composition comprising human allogeneic myeloid progenitor cells derived from multiple unrelated donors in an amount sufficient to improve hematopoiesis in the human, wherein there is at least a partial mismatch at a major histocompatability complex (MHC) gene between the donors and the human.   
     
     
         2 . The method of  claim 1 , wherein the composition has less than 10% .hematopoietic stem cells (HSCs). 
     
     
         3 . The method of  claim 1 , wherein human allogeneic myeloid progenitor cells are expanded human allogeneic myeloid progenitor cells. 
     
     
         4 . The method of  claim 1 , wherein the myeloid progenitor cells comprise common myeloid progenitor cells. 
     
     
         5 . The method of  claim 1 , wherein myeloid progenitor cells in the composition are at least 25% of total cells in the composition. 
     
     
         6 . The method of  claim 1 , wherein the human is undergoing hematopoietic stem cell (HSC) transplantation. 
     
     
         7 . The method of  claim 6 , wherein the expanded myeloid progenitor cells are administered after the HSC transplantation 
     
     
         8 . The method of  claim 6 , wherein the expanded myeloid progenitor cells are administered concurrently with HSC transplantation. 
     
     
         9 . The method of  claim 1 , wherein the human is neutropenic. 
     
     
         10 . The method of  claim 1 , wherein the human is suffering from thrombocytopenia. 
     
     
         11 . The method of  claim 10 , wherein the expanded myeloid progenitor cells are administered adjunctively with a therapeutic composition for treating complications associated with thrombocytopenia. 
     
     
         12 . The method of  claim 11 , wherein the therapeutic composition comprises a platelet preparation. 
     
     
         13 . The method of  claim 11 , wherein the therapeutic composition comprises EPO. 
     
     
         14 . The method of  claim 1 , wherein the myeloid progenitor cells are expanded from cells obtained from peripheral blood. 
     
     
         15 . The method of  claim 1 , wherein the myeloid progenitor cells are expanded from cells obtained from bone marrow. 
     
     
         16 . The method of  claim 1 , wherein the myeloid progenitor cells are expanded from cells obtained from umbilical cord blood or placental cord blood. 
     
     
         17 . The method of  claim 1 , wherein the human has been previously treated with or exposed to a myeloablative agent. 
     
     
         18 . The method of  claim 17 , wherein the myeloablative agent is ionizing radiation.

Cited by (0)

No later patents cite this yet.

References (0)

No backward citations on record.