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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 |
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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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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</description><identifier>ISSN: 0892-6638</identifier><identifier>EISSN: 1530-6860</identifier><identifier>DOI: 10.1096/fj.14-268144</identifier><identifier>PMID: 25746794</identifier><language>eng</language><publisher>United States: Federation of American Societies for Experimental Biology</publisher><subject>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</subject><ispartof>The FASEB journal, 2015-06, Vol.29 (6), p.2595-2602</ispartof><rights>FASEB</rights><rights>FASEB.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3734-cdb2f3d0a6abcf37581c75841ebc6abfffb73325e6d65e4fb066acf9b28e09df3</citedby><cites>FETCH-LOGICAL-c3734-cdb2f3d0a6abcf37581c75841ebc6abfffb73325e6d65e4fb066acf9b28e09df3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25746794$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Reed, Daniel M.</creatorcontrib><creatorcontrib>Paschalaki, Koralia E.</creatorcontrib><creatorcontrib>Starke, Richard D.</creatorcontrib><creatorcontrib>Mohamed, Nura A.</creatorcontrib><creatorcontrib>Sharp, Giles</creatorcontrib><creatorcontrib>Fox, Bernard</creatorcontrib><creatorcontrib>Eastwood, David</creatorcontrib><creatorcontrib>Bristow, Adrian</creatorcontrib><creatorcontrib>Ball, Christina</creatorcontrib><creatorcontrib>Vessillier, Sandrine</creatorcontrib><creatorcontrib>Hansel, Trevor T.</creatorcontrib><creatorcontrib>Thorpe, Susan J.</creatorcontrib><creatorcontrib>Randi, Anna M.</creatorcontrib><creatorcontrib>Stebbings, Richard</creatorcontrib><creatorcontrib>Mitchell, Jane A.</creatorcontrib><title>An autologous endothelial cell:peripheral blood mononuclear cell assay that detects cytokine storm responses to biologics</title><title>The FASEB journal</title><addtitle>FASEB J</addtitle><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</description><subject>Alemtuzumab</subject><subject>Antibodies, Monoclonal - pharmacology</subject><subject>Antibodies, Monoclonal, Humanized - pharmacology</subject><subject>Bevacizumab</subject><subject>Biological Assay - methods</subject><subject>Biological Products - pharmacology</subject><subject>Cell Proliferation - drug effects</subject><subject>coculture</subject><subject>Coculture Techniques</subject><subject>Culture Media - pharmacology</subject><subject>Cytokines - metabolism</subject><subject>Endothelial Cells - cytology</subject><subject>Endothelial Cells - drug effects</subject><subject>Endothelial Cells - metabolism</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Human Umbilical Vein Endothelial Cells - cytology</subject><subject>Human Umbilical Vein Endothelial Cells - drug effects</subject><subject>Human Umbilical Vein Endothelial Cells - metabolism</subject><subject>Humans</subject><subject>Interleukin-2 - metabolism</subject><subject>Interleukin-6 - metabolism</subject><subject>Interleukin-8 - metabolism</subject><subject>Leukocytes, Mononuclear - cytology</subject><subject>Leukocytes, Mononuclear - drug effects</subject><subject>Leukocytes, Mononuclear - metabolism</subject><subject>personalized medicine</subject><subject>Reproducibility of Results</subject><subject>Serum - chemistry</subject><subject>stem cells</subject><subject>TGN1412</subject><subject>Trastuzumab</subject><subject>Tumor Necrosis Factor-alpha - metabolism</subject><issn>0892-6638</issn><issn>1530-6860</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqFkU1v1DAQhi1ERbeFG2fkIwdS7PgjDre2YguoUg8tZ8t2xmwWJw62I5R_T5ZdOMJhZjSjR-_M6EXoNSVXlLTyvd9fUV7VUlHOn6ENFYxUUknyHG2IautKSqbO0UXOe0IIJVS-QOe1aLhsWr5By_WIzVxiiN_inDGMXSw7CL0J2EEIHyZI_bSDtPY2xNjhIY5xnF0Ak34T2ORsFlx2puAOCriSsVtK_N6PgHOJacAJ8hTHDBmXiG1_2NW7_BKdeRMyvDrVS_R1-_Hp9lN1_3D3-fb6vnKsYbxyna0964iRxjrPGqGoWxOnYN068t7bhrFagOykAO4tkdI439paAWk7zy7R26PulOKPGXLRQ58Pl5sR1pc1VUTJNYT4PyqVaASrSbOi746oSzHnBF5PqR9MWjQl-uCL9ntNuT76suJvTsqzHaD7C_8xYgXUEfjZB1j-Kaa3jzf19gvlJ-1fC3ic3g</recordid><startdate>201506</startdate><enddate>201506</enddate><creator>Reed, Daniel M.</creator><creator>Paschalaki, Koralia E.</creator><creator>Starke, Richard D.</creator><creator>Mohamed, Nura A.</creator><creator>Sharp, Giles</creator><creator>Fox, Bernard</creator><creator>Eastwood, David</creator><creator>Bristow, Adrian</creator><creator>Ball, Christina</creator><creator>Vessillier, Sandrine</creator><creator>Hansel, Trevor T.</creator><creator>Thorpe, Susan J.</creator><creator>Randi, Anna M.</creator><creator>Stebbings, Richard</creator><creator>Mitchell, Jane A.</creator><general>Federation of American Societies for Experimental Biology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7T5</scope><scope>H94</scope></search><sort><creationdate>201506</creationdate><title>An autologous endothelial cell:peripheral blood mononuclear cell assay that detects cytokine storm responses to biologics</title><author>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.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3734-cdb2f3d0a6abcf37581c75841ebc6abfffb73325e6d65e4fb066acf9b28e09df3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Alemtuzumab</topic><topic>Antibodies, Monoclonal - pharmacology</topic><topic>Antibodies, Monoclonal, Humanized - pharmacology</topic><topic>Bevacizumab</topic><topic>Biological Assay - methods</topic><topic>Biological Products - pharmacology</topic><topic>Cell Proliferation - drug effects</topic><topic>coculture</topic><topic>Coculture Techniques</topic><topic>Culture Media - pharmacology</topic><topic>Cytokines - metabolism</topic><topic>Endothelial Cells - cytology</topic><topic>Endothelial Cells - drug effects</topic><topic>Endothelial Cells - metabolism</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Human Umbilical Vein Endothelial Cells - cytology</topic><topic>Human Umbilical Vein Endothelial Cells - drug effects</topic><topic>Human Umbilical Vein Endothelial Cells - metabolism</topic><topic>Humans</topic><topic>Interleukin-2 - metabolism</topic><topic>Interleukin-6 - metabolism</topic><topic>Interleukin-8 - metabolism</topic><topic>Leukocytes, Mononuclear - cytology</topic><topic>Leukocytes, Mononuclear - drug effects</topic><topic>Leukocytes, Mononuclear - metabolism</topic><topic>personalized medicine</topic><topic>Reproducibility of Results</topic><topic>Serum - chemistry</topic><topic>stem cells</topic><topic>TGN1412</topic><topic>Trastuzumab</topic><topic>Tumor Necrosis Factor-alpha - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Reed, Daniel M.</creatorcontrib><creatorcontrib>Paschalaki, Koralia E.</creatorcontrib><creatorcontrib>Starke, Richard D.</creatorcontrib><creatorcontrib>Mohamed, Nura A.</creatorcontrib><creatorcontrib>Sharp, Giles</creatorcontrib><creatorcontrib>Fox, Bernard</creatorcontrib><creatorcontrib>Eastwood, David</creatorcontrib><creatorcontrib>Bristow, Adrian</creatorcontrib><creatorcontrib>Ball, Christina</creatorcontrib><creatorcontrib>Vessillier, Sandrine</creatorcontrib><creatorcontrib>Hansel, Trevor T.</creatorcontrib><creatorcontrib>Thorpe, Susan J.</creatorcontrib><creatorcontrib>Randi, Anna M.</creatorcontrib><creatorcontrib>Stebbings, Richard</creatorcontrib><creatorcontrib>Mitchell, Jane A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>The FASEB journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Reed, Daniel M.</au><au>Paschalaki, Koralia E.</au><au>Starke, Richard D.</au><au>Mohamed, Nura A.</au><au>Sharp, Giles</au><au>Fox, Bernard</au><au>Eastwood, David</au><au>Bristow, Adrian</au><au>Ball, Christina</au><au>Vessillier, Sandrine</au><au>Hansel, Trevor T.</au><au>Thorpe, Susan J.</au><au>Randi, Anna M.</au><au>Stebbings, Richard</au><au>Mitchell, Jane A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An autologous endothelial cell:peripheral blood mononuclear cell assay that detects cytokine storm responses to biologics</atitle><jtitle>The FASEB journal</jtitle><addtitle>FASEB J</addtitle><date>2015-06</date><risdate>2015</risdate><volume>29</volume><issue>6</issue><spage>2595</spage><epage>2602</epage><pages>2595-2602</pages><issn>0892-6638</issn><eissn>1530-6860</eissn><abstract>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</abstract><cop>United States</cop><pub>Federation of American Societies for Experimental Biology</pub><pmid>25746794</pmid><doi>10.1096/fj.14-268144</doi><tpages>8</tpages></addata></record> |
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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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