US2017003280A1PendingUtilityA1

In vitro assays for inhibition of microglial activation

Assignee: THE J DAVID GLADSTONE INSTPriority: Jan 11, 2014Filed: Jan 9, 2015Published: Jan 5, 2017
Est. expiryJan 11, 2034(~7.5 yrs left)· nominal 20-yr term from priority
G01N 33/5047G01N 2800/28A61P 25/28G01N 2500/00G01N 33/5058G01N 33/502G01N 33/5008G01N 33/5044G01N 33/5014G01N 2800/7095
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Claims

Abstract

The present invention provides cell-based assays, including high throughput cell-based assays, for identification of candidate therapeutic agent with no known agents with the ability to inhibit microglial activation in vivo in response to different ligands.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A cell-based assay for identification of candidate therapeutic agents that inhibit microglia activation in vivo, comprising:
 providing in vitro activated microglial cells;   contacting said activated microglial cells with one or more test agents;   identifying one or more test agents that exhibit inhibition of the in vitro microglia activation; and   determining toxicity of the identified test agents that exhibit inhibition of the in vitro microglia activation by determination of cell death upon exposure of the microglial cells to the test agents;   wherein the test agents that exhibit both inhibition of the in vitro microglia activation and lack of toxicity are candidate therapeutic agents for the inhibition of microglial activation in vivo.   
     
     
         2 . The assay of  claim 1 , further comprising the step of activating microglial cells in vitro using an agent associated with microglial activation. 
     
     
         3 . The assay of  claims 1  and  2 , wherein the microglial cells are activated by in vitro exposure to an active fibrin composition. 
     
     
         4 . The assay of  claims 1  and  2 , wherein the microglial cells are activated by in vitro exposure to LPS. 
     
     
         5 . The assay of  claim 1  through  4 , wherein the candidate therapeutic agents exhibit at least a 50% inhibition of the in vitro microglia activation. 
     
     
         6 . The assay of  claims 1  through  5 , wherein the toxicity is measured through identification of cell death of the activated microglial cells. 
     
     
         7 . The assay of  claim 6 , wherein the cell death is identified through shrinkage of the cell surface area of the microglia. 
     
     
         8 . The assay of  claims 6  and  7 , wherein the cell death is identified through shrinkage of the cell surface area of the microglia to 150 μm 2  or less. 
     
     
         9 . The assay of  claims 1  through  8 , wherein the one or more test agents comprise agents with demonstrated affinity to targets involved in microglia activation. 
     
     
         10 . The assay of  claims 1  through  9 , wherein the one or more test agents comprise known drugs with clinical evaluation data. 
     
     
         11 . The assay of  claims 1  through  10 , wherein the one or more test agents comprise known anti-inflammatory and microglia-macrophage response modulators. 
     
     
         12 . The assay of  claims 1  through  8 , wherein the one or more test agents comprise agents with no known activity or identified binding target. 
     
     
         13 . A high-throughput cell-based assay for identifying a candidate therapeutically active agent for clinical inhibition of microglia activation, comprising the steps of:
 providing a panel of in vitro activated microglial cells;   contacting said panel of microglial cells with one or more individual test agents;   determining whether the test agents cause inhibition of the activation of the microglial cells treated with the test agents; and   determining the level of cell death of the microglial cells treated with the test agents;   wherein the one or more test agents that exhibit inhibition of the activation of the microglial cells and no increased cell death are candidate therapeutically active agents for clinical inhibition of microglia activation in vivo.   
     
     
         14 . The assay of  claim 13 , further comprising the step of activating microglial cells in vitro using an agent associated with microglial activation. 
     
     
         15 . The assay of  claim 14 , wherein the microglial cells are activated by in vitro exposure to an active fibrin composition. 
     
     
         16 . The assay of  claim 14 , wherein the microglial cells are activated by in vitro exposure to LPS. 
     
     
         17 . The assay of  claims 13  through  16 , wherein the toxicity is measured through identification of cell death of the activated microglial cells 
     
     
         18 . The assay of  claim 17 , wherein the cell death is identified through shrinkage of the cell surface area of the microglia. 
     
     
         19 . The assay of  claims 17  and  18 , wherein the cell death is identified through shrinkage of the cell surface area of the microglia to 150 μm 2  or less. 
     
     
         20 . The assay of  claims 13  through  19 , wherein the one or more test agents comprise agents with demonstrated affinity to targets involved in microglia activation. 
     
     
         21 . The assay of  claims 13  through  20 , wherein the one or more test agents comprise known drugs with clinical evaluation data. 
     
     
         22 . The assay of  claims 13  through  21 , wherein the one or more test agents comprise known anti-inflammatory and microglia-macrophage response modulators. 
     
     
         23 . The assay of  claims 13  through  19 , wherein the one or more test agents comprise agents with no known activity or identified binding target.

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