US2022370503A1PendingUtilityA1

Methods and devices for the production and delivery of beneficial factors from stem cells

Assignee: AELAN CELL TECH INCPriority: Jun 3, 2015Filed: Mar 31, 2022Published: Nov 24, 2022
Est. expiryJun 3, 2035(~8.8 yrs left)· nominal 20-yr term from priority
C12Q 2600/142C12Q 2600/158C12Q 1/6883G01N 33/575G01N 2333/495A61K 38/43C12N 5/0667G01N 2333/705G01N 2333/55C12N 2501/2302C12N 2501/65A61K 35/28C07K 16/246A61P 35/00G01N 2333/91205G01N 2333/4703A61K 38/2013C12N 5/0663G01N 2333/96466C12N 5/0018G01N 2333/96486G01N 2333/475C12Q 1/6886G01N 33/574
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Claims

Abstract

Provided herein are methods and devices related to inducing a population of self-renewing or senescent stem cells, to produce one or more beneficial factors for the treatment of a disease or disorder in an individual. Also provided are compositions and methods for inducing senescence, useful for inducing senescence in a population of stem cells, in order to produce one or more beneficial factors for the treatment of a disease or disorder in an individual. Methods and devices to control and customize the production of the beneficial factors for the requirements of a disease or disorder being treated are described. Also provided are factor production units for the production of the beneficial factors, and devices for the delivery of the beneficial factors to an individual in need.

Claims

exact text as granted — not AI-modified
1 .- 74 . (canceled) 
     
     
         75 . A method of expanding regulatory T-cell (Tregs), the method comprising:
 growing a population of human adipose derived stem cells (hADSCs);   adding an inducing agent comprising IL-2 to the population of hADSCs for about 24 hours to induce the production of the one or more secreted factors by the population of hADSCs;   collecting the one more secreted factors about 72 hours post-induction; and   contacting peripheral blood mononuclear cells (PBMCs) with the one or more secreted factors to induce expansion of the Tregs.   
     
     
         76 . The method of  claim 75 , wherein the population of hADSCs comprise self-renewing (SR) cells and senescent (SEN) cells. 
     
     
         77 . The method of  claim 75 , wherein the population of hADSCs comprise at least 50% SR cells. 
     
     
         78 . The method of  claim 75 , wherein the population of hADSCs comprise at least 50% SEN cells. 
     
     
         79 . The method of  claim 75 , wherein the secreted factors are produced in a factor production unit. 
     
     
         80 . A method for modulating immune cells, the method comprising:
 providing a population of human adipose derived stem cells (hADSCs);   adding an inducing agent comprising IL-2 to the population of hADSCs for about 24 hours to induce the production of one or more secreted factors by the population of hADSCs;   collecting the one more secreted factors about 72 hours post-induction; and   contacting immune cells of a subject with the one or more secreted factors to immunomodulate the immune cells.   
     
     
         81 . The method of  claim 80 , wherein the one or more secreted factors are administered to a subject. 
     
     
         82 . The method of  claim 80 , wherein the one or more secreted factors are contacted with the immune cells ex vivo. 
     
     
         83 . The method of  claim 82 , wherein the immune cells are collected from a blood sample or a plasma sample from a subject. 
     
     
         84 . The method of  claim 83 , further comprising delivering the immunomodulated immune cells back into the subject. 
     
     
         85 . The method of  claim 80 , wherein the immune cells comprise peripheral blood mononuclear cells (PBMCs). 
     
     
         86 . The method of  claim 80 , wherein the immunomodulated immune cells comprise regulatory T-cell (Tregs). 
     
     
         87 . The method of  claim 85 , wherein the modulating of the immune cells comprises increasing production of the Tregs from the immune cells. 
     
     
         88 . The method of  claim 80 , wherein the population of hADSCs comprise self-renewing (SR) cells and senescent (SEN) cells. 
     
     
         89 . The method of  claim 80 , wherein the population of hADSCs comprise at least 50% SR cells. 
     
     
         90 . The method of  claim 80 , wherein the population of hADSCs comprise at least 50% SEN cells. 
     
     
         91 . The method of  claim 80 , wherein the population of hADSCs are provided in a factor production unit.

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