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An autologous endothelial cell:peripheral blood mononuclear cell assay that detects cytokine storm responses to biologics

ABSTRACT There is an urgent unmet need for human tissue bioassays to predict cytokine storm responses to biologics. Current bioassays that detect cytokine storm responses in vitro rely on endothelial cells, usually from umbilical veins or cell lines, cocultured with freshly isolated peripheral blood...

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Published in:The FASEB journal 2015-06, Vol.29 (6), p.2595-2602
Main Authors: Reed, Daniel M., Paschalaki, Koralia E., Starke, Richard D., Mohamed, Nura A., Sharp, Giles, Fox, Bernard, Eastwood, David, Bristow, Adrian, Ball, Christina, Vessillier, Sandrine, Hansel, Trevor T., Thorpe, Susan J., Randi, Anna M., Stebbings, Richard, Mitchell, Jane A.
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cited_by cdi_FETCH-LOGICAL-c3734-cdb2f3d0a6abcf37581c75841ebc6abfffb73325e6d65e4fb066acf9b28e09df3
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creator Reed, Daniel M.
Paschalaki, Koralia E.
Starke, Richard D.
Mohamed, Nura A.
Sharp, Giles
Fox, Bernard
Eastwood, David
Bristow, Adrian
Ball, Christina
Vessillier, Sandrine
Hansel, Trevor T.
Thorpe, Susan J.
Randi, Anna M.
Stebbings, Richard
Mitchell, Jane A.
description ABSTRACT There is an urgent unmet need for human tissue bioassays to predict cytokine storm responses to biologics. Current bioassays that detect cytokine storm responses in vitro rely on endothelial cells, usually from umbilical veins or cell lines, cocultured with freshly isolated peripheral blood mononuclear cells (PBMCs) from healthy adult volunteers. These assays therefore comprise cells from 2 separate donors and carry the disadvantage of mismatched tissues and lack the advantage of personalized medicine. Current assays also do not fully delineate mild (such as Campath) and severe (such as TGN1412) cytokine storm‐inducing drugs. Here, we report a novel bioassay where endothelial cells grown from stem cells in the peripheral blood (blood outgrowth endothelial cells) and PBMCs from the same donor can be used to create an autologous coculture bioassay that responds by releasing a plethora of cytokines to authentic TGN1412 but only modestly to Campath and not to control antibodies such as Herceptin, Avastin, and Arzerra. This assay performed better than the traditional mixed donor assay in terms of cytokine release to TGN1412 and, thus, we suggest provides significant advancement and a definitive system by which biologics can be tested and paves the way for personalized medicine.—Reed, D. M., Paschalaki, K. E., Starke, R. D., Mohamed, N. A., Sharp, G., Fox, B., Eastwood, D., Bristow, A., Ball, C., Vessillier, S., Hansel, T. T., Thorpe, S. J., Randi, A. M., Stebbings, R., Mitchell, J. A. An autologous endothelial cell:peripheral blood mononuclear cell assay that detects cytokine storm responses to biologics. FASEB J. 29, 2595‐2602 (2015). www.fasebj.org
doi_str_mv 10.1096/fj.14-268144
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Current bioassays that detect cytokine storm responses in vitro rely on endothelial cells, usually from umbilical veins or cell lines, cocultured with freshly isolated peripheral blood mononuclear cells (PBMCs) from healthy adult volunteers. These assays therefore comprise cells from 2 separate donors and carry the disadvantage of mismatched tissues and lack the advantage of personalized medicine. Current assays also do not fully delineate mild (such as Campath) and severe (such as TGN1412) cytokine storm‐inducing drugs. Here, we report a novel bioassay where endothelial cells grown from stem cells in the peripheral blood (blood outgrowth endothelial cells) and PBMCs from the same donor can be used to create an autologous coculture bioassay that responds by releasing a plethora of cytokines to authentic TGN1412 but only modestly to Campath and not to control antibodies such as Herceptin, Avastin, and Arzerra. 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Current bioassays that detect cytokine storm responses in vitro rely on endothelial cells, usually from umbilical veins or cell lines, cocultured with freshly isolated peripheral blood mononuclear cells (PBMCs) from healthy adult volunteers. These assays therefore comprise cells from 2 separate donors and carry the disadvantage of mismatched tissues and lack the advantage of personalized medicine. Current assays also do not fully delineate mild (such as Campath) and severe (such as TGN1412) cytokine storm‐inducing drugs. Here, we report a novel bioassay where endothelial cells grown from stem cells in the peripheral blood (blood outgrowth endothelial cells) and PBMCs from the same donor can be used to create an autologous coculture bioassay that responds by releasing a plethora of cytokines to authentic TGN1412 but only modestly to Campath and not to control antibodies such as Herceptin, Avastin, and Arzerra. 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subjects Alemtuzumab
Antibodies, Monoclonal - pharmacology
Antibodies, Monoclonal, Humanized - pharmacology
Bevacizumab
Biological Assay - methods
Biological Products - pharmacology
Cell Proliferation - drug effects
coculture
Coculture Techniques
Culture Media - pharmacology
Cytokines - metabolism
Endothelial Cells - cytology
Endothelial Cells - drug effects
Endothelial Cells - metabolism
Enzyme-Linked Immunosorbent Assay
Human Umbilical Vein Endothelial Cells - cytology
Human Umbilical Vein Endothelial Cells - drug effects
Human Umbilical Vein Endothelial Cells - metabolism
Humans
Interleukin-2 - metabolism
Interleukin-6 - metabolism
Interleukin-8 - metabolism
Leukocytes, Mononuclear - cytology
Leukocytes, Mononuclear - drug effects
Leukocytes, Mononuclear - metabolism
personalized medicine
Reproducibility of Results
Serum - chemistry
stem cells
TGN1412
Trastuzumab
Tumor Necrosis Factor-alpha - metabolism
title An autologous endothelial cell:peripheral blood mononuclear cell assay that detects cytokine storm responses to biologics
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