Supplementary Material for: Autologous Peripheral Blood Mononuclear Cells as Treatment in Refractory Acute Respiratory Distress Syndrome

Background: Acute respiratory distress syndrome (ARDS) is a devastating disorder. Despite enormous efforts in clinical research, effective treatment options are lacking, and mortality rates remain unacceptably high. Objectives: A male patient with severe ARDS showed no clinical improvement with conv...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Jungebluth, P., Holzgraefe, B., Lim, M.L., Duru, A.D., Lundin, V., Heldring, N., Wiklander O.P.B., Nordin, J.Z., Chrobok, M., Roderburg, C., Sjöqvist, S., Anderstam, B., Beltrán Rodríguez, A., Haag, J.C., Gustafsson, Y., Roddewig, K.G., Jones, P., Wood M.J.A., Luedde T.J, Teixeira, A.I., Hermanson, O., Winqvist, O., Kalzén, H., El Andaloussi, S., Alici, E., Macchiarini, P.
Format: Dataset
Sprache:eng
Schlagworte:
Online-Zugang:Volltext bestellen
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue
container_start_page
container_title
container_volume
creator Jungebluth, P.
Holzgraefe, B.
Lim, M.L.
Duru, A.D.
Lundin, V.
Heldring, N.
Wiklander O.P.B.
Nordin, J.Z.
Chrobok, M.
Roderburg, C.
Sjöqvist, S.
Anderstam, B.
Beltrán Rodríguez, A.
Haag, J.C.
Gustafsson, Y.
Roddewig, K.G.
Jones, P.
Wood M.J.A.
Luedde T.J
Teixeira, A.I.
Hermanson, O.
Winqvist, O.
Kalzén, H.
El Andaloussi, S.
Alici, E.
Macchiarini, P.
description Background: Acute respiratory distress syndrome (ARDS) is a devastating disorder. Despite enormous efforts in clinical research, effective treatment options are lacking, and mortality rates remain unacceptably high. Objectives: A male patient with severe ARDS showed no clinical improvement with conventional therapies. Hence, an emergent experimental intervention was performed. Methods: We performed intratracheal administration of autologous peripheral blood-derived mononuclear cells (PBMCs) and erythropoietin (EPO). Results: We found that after 2 days of initial PBMC/EPO application, lung function improved and extracorporeal membrane oxygenation (ECMO) support was reduced. Bronchoscopy and serum inflammatory markers revealed reduced inflammation. Additionally, serum concentration of miR-449a, b, c and miR-34a, a transient upregulation of E-cadherin and associated chromatin marks in PBMCs indicated airway epithelial differentiation. Extracellular vesicles from PBMCs demonstrated anti-inflammatory capacity in a TNF-a-mediated nuclear factor-κB in vitro assay. Despite improving respiratory function, the patient died of multisystem organ failure on day 38 of ECMO treatment. Conclusions: This case report provides initial encouraging evidence to use locally instilled PBMC/EPO for treatment of severe refractory ARDS. The observed clinical improvement may partially be due to the anti-inflammatory effects of PBMC/EPO to promote tissue regeneration. Further studies are needed for more in-depth understanding of the underlying mechanisms of in vivo regeneration.
doi_str_mv 10.6084/m9.figshare.4047357
format Dataset
fullrecord <record><control><sourceid>datacite_PQ8</sourceid><recordid>TN_cdi_datacite_primary_10_6084_m9_figshare_4047357</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_6084_m9_figshare_4047357</sourcerecordid><originalsourceid>FETCH-LOGICAL-d897-5a544516d5125e1dab39028831a97e010585ef82b00b06bcdfbd316bf756c1b03</originalsourceid><addsrcrecordid>eNo1kE1OwzAQRrNhgQonYOMLpNh1nB92pfxKrUA0e2scj1tLThzZzqI34NikUFYjvZGe9L0su2N0WdK6uO-bpbGHeISAy4IWFRfVdfa9n8bRYY9DgnAiO0gYLDhifHgg6yl55w9-iuRzxuMRw_x6dN5rsvODH6bOIQSyQecigUjagJDOLmIH8oUmQJf8rF13U8IZxNEG-CVPNqaAMZL9adDB93iTXRlwEW8vd5G1L8_t5i3ffry-b9bbXNdNlQsQRSFYqQVbCWQaFG_oqq45g6ZCyqioBZp6pShVtFSdNkpzVipTibJjivJFxv-0GhJ0NqEcg-3n6ZJRec4k-0b-Z5KXTPwHo8NnOQ</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>dataset</recordtype></control><display><type>dataset</type><title>Supplementary Material for: Autologous Peripheral Blood Mononuclear Cells as Treatment in Refractory Acute Respiratory Distress Syndrome</title><source>DataCite</source><creator>Jungebluth, P. ; Holzgraefe, B. ; Lim, M.L. ; Duru, A.D. ; Lundin, V. ; Heldring, N. ; Wiklander O.P.B. ; Nordin, J.Z. ; Chrobok, M. ; Roderburg, C. ; Sjöqvist, S. ; Anderstam, B. ; Beltrán Rodríguez, A. ; Haag, J.C. ; Gustafsson, Y. ; Roddewig, K.G. ; Jones, P. ; Wood M.J.A. ; Luedde T.J ; Teixeira, A.I. ; Hermanson, O. ; Winqvist, O. ; Kalzén, H. ; El Andaloussi, S. ; Alici, E. ; Macchiarini, P.</creator><creatorcontrib>Jungebluth, P. ; Holzgraefe, B. ; Lim, M.L. ; Duru, A.D. ; Lundin, V. ; Heldring, N. ; Wiklander O.P.B. ; Nordin, J.Z. ; Chrobok, M. ; Roderburg, C. ; Sjöqvist, S. ; Anderstam, B. ; Beltrán Rodríguez, A. ; Haag, J.C. ; Gustafsson, Y. ; Roddewig, K.G. ; Jones, P. ; Wood M.J.A. ; Luedde T.J ; Teixeira, A.I. ; Hermanson, O. ; Winqvist, O. ; Kalzén, H. ; El Andaloussi, S. ; Alici, E. ; Macchiarini, P.</creatorcontrib><description>Background: Acute respiratory distress syndrome (ARDS) is a devastating disorder. Despite enormous efforts in clinical research, effective treatment options are lacking, and mortality rates remain unacceptably high. Objectives: A male patient with severe ARDS showed no clinical improvement with conventional therapies. Hence, an emergent experimental intervention was performed. Methods: We performed intratracheal administration of autologous peripheral blood-derived mononuclear cells (PBMCs) and erythropoietin (EPO). Results: We found that after 2 days of initial PBMC/EPO application, lung function improved and extracorporeal membrane oxygenation (ECMO) support was reduced. Bronchoscopy and serum inflammatory markers revealed reduced inflammation. Additionally, serum concentration of miR-449a, b, c and miR-34a, a transient upregulation of E-cadherin and associated chromatin marks in PBMCs indicated airway epithelial differentiation. Extracellular vesicles from PBMCs demonstrated anti-inflammatory capacity in a TNF-a-mediated nuclear factor-κB in vitro assay. Despite improving respiratory function, the patient died of multisystem organ failure on day 38 of ECMO treatment. Conclusions: This case report provides initial encouraging evidence to use locally instilled PBMC/EPO for treatment of severe refractory ARDS. The observed clinical improvement may partially be due to the anti-inflammatory effects of PBMC/EPO to promote tissue regeneration. Further studies are needed for more in-depth understanding of the underlying mechanisms of in vivo regeneration.</description><identifier>DOI: 10.6084/m9.figshare.4047357</identifier><language>eng</language><publisher>Karger Publishers</publisher><subject>Medicine</subject><creationdate>2016</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>780,1892</link.rule.ids><linktorsrc>$$Uhttps://commons.datacite.org/doi.org/10.6084/m9.figshare.4047357$$EView_record_in_DataCite.org$$FView_record_in_$$GDataCite.org$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>Jungebluth, P.</creatorcontrib><creatorcontrib>Holzgraefe, B.</creatorcontrib><creatorcontrib>Lim, M.L.</creatorcontrib><creatorcontrib>Duru, A.D.</creatorcontrib><creatorcontrib>Lundin, V.</creatorcontrib><creatorcontrib>Heldring, N.</creatorcontrib><creatorcontrib>Wiklander O.P.B.</creatorcontrib><creatorcontrib>Nordin, J.Z.</creatorcontrib><creatorcontrib>Chrobok, M.</creatorcontrib><creatorcontrib>Roderburg, C.</creatorcontrib><creatorcontrib>Sjöqvist, S.</creatorcontrib><creatorcontrib>Anderstam, B.</creatorcontrib><creatorcontrib>Beltrán Rodríguez, A.</creatorcontrib><creatorcontrib>Haag, J.C.</creatorcontrib><creatorcontrib>Gustafsson, Y.</creatorcontrib><creatorcontrib>Roddewig, K.G.</creatorcontrib><creatorcontrib>Jones, P.</creatorcontrib><creatorcontrib>Wood M.J.A.</creatorcontrib><creatorcontrib>Luedde T.J</creatorcontrib><creatorcontrib>Teixeira, A.I.</creatorcontrib><creatorcontrib>Hermanson, O.</creatorcontrib><creatorcontrib>Winqvist, O.</creatorcontrib><creatorcontrib>Kalzén, H.</creatorcontrib><creatorcontrib>El Andaloussi, S.</creatorcontrib><creatorcontrib>Alici, E.</creatorcontrib><creatorcontrib>Macchiarini, P.</creatorcontrib><title>Supplementary Material for: Autologous Peripheral Blood Mononuclear Cells as Treatment in Refractory Acute Respiratory Distress Syndrome</title><description>Background: Acute respiratory distress syndrome (ARDS) is a devastating disorder. Despite enormous efforts in clinical research, effective treatment options are lacking, and mortality rates remain unacceptably high. Objectives: A male patient with severe ARDS showed no clinical improvement with conventional therapies. Hence, an emergent experimental intervention was performed. Methods: We performed intratracheal administration of autologous peripheral blood-derived mononuclear cells (PBMCs) and erythropoietin (EPO). Results: We found that after 2 days of initial PBMC/EPO application, lung function improved and extracorporeal membrane oxygenation (ECMO) support was reduced. Bronchoscopy and serum inflammatory markers revealed reduced inflammation. Additionally, serum concentration of miR-449a, b, c and miR-34a, a transient upregulation of E-cadherin and associated chromatin marks in PBMCs indicated airway epithelial differentiation. Extracellular vesicles from PBMCs demonstrated anti-inflammatory capacity in a TNF-a-mediated nuclear factor-κB in vitro assay. Despite improving respiratory function, the patient died of multisystem organ failure on day 38 of ECMO treatment. Conclusions: This case report provides initial encouraging evidence to use locally instilled PBMC/EPO for treatment of severe refractory ARDS. The observed clinical improvement may partially be due to the anti-inflammatory effects of PBMC/EPO to promote tissue regeneration. Further studies are needed for more in-depth understanding of the underlying mechanisms of in vivo regeneration.</description><subject>Medicine</subject><fulltext>true</fulltext><rsrctype>dataset</rsrctype><creationdate>2016</creationdate><recordtype>dataset</recordtype><sourceid>PQ8</sourceid><recordid>eNo1kE1OwzAQRrNhgQonYOMLpNh1nB92pfxKrUA0e2scj1tLThzZzqI34NikUFYjvZGe9L0su2N0WdK6uO-bpbGHeISAy4IWFRfVdfa9n8bRYY9DgnAiO0gYLDhifHgg6yl55w9-iuRzxuMRw_x6dN5rsvODH6bOIQSyQecigUjagJDOLmIH8oUmQJf8rF13U8IZxNEG-CVPNqaAMZL9adDB93iTXRlwEW8vd5G1L8_t5i3ffry-b9bbXNdNlQsQRSFYqQVbCWQaFG_oqq45g6ZCyqioBZp6pShVtFSdNkpzVipTibJjivJFxv-0GhJ0NqEcg-3n6ZJRec4k-0b-Z5KXTPwHo8NnOQ</recordid><startdate>20161021</startdate><enddate>20161021</enddate><creator>Jungebluth, P.</creator><creator>Holzgraefe, B.</creator><creator>Lim, M.L.</creator><creator>Duru, A.D.</creator><creator>Lundin, V.</creator><creator>Heldring, N.</creator><creator>Wiklander O.P.B.</creator><creator>Nordin, J.Z.</creator><creator>Chrobok, M.</creator><creator>Roderburg, C.</creator><creator>Sjöqvist, S.</creator><creator>Anderstam, B.</creator><creator>Beltrán Rodríguez, A.</creator><creator>Haag, J.C.</creator><creator>Gustafsson, Y.</creator><creator>Roddewig, K.G.</creator><creator>Jones, P.</creator><creator>Wood M.J.A.</creator><creator>Luedde T.J</creator><creator>Teixeira, A.I.</creator><creator>Hermanson, O.</creator><creator>Winqvist, O.</creator><creator>Kalzén, H.</creator><creator>El Andaloussi, S.</creator><creator>Alici, E.</creator><creator>Macchiarini, P.</creator><general>Karger Publishers</general><scope>DYCCY</scope><scope>PQ8</scope></search><sort><creationdate>20161021</creationdate><title>Supplementary Material for: Autologous Peripheral Blood Mononuclear Cells as Treatment in Refractory Acute Respiratory Distress Syndrome</title><author>Jungebluth, P. ; Holzgraefe, B. ; Lim, M.L. ; Duru, A.D. ; Lundin, V. ; Heldring, N. ; Wiklander O.P.B. ; Nordin, J.Z. ; Chrobok, M. ; Roderburg, C. ; Sjöqvist, S. ; Anderstam, B. ; Beltrán Rodríguez, A. ; Haag, J.C. ; Gustafsson, Y. ; Roddewig, K.G. ; Jones, P. ; Wood M.J.A. ; Luedde T.J ; Teixeira, A.I. ; Hermanson, O. ; Winqvist, O. ; Kalzén, H. ; El Andaloussi, S. ; Alici, E. ; Macchiarini, P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-d897-5a544516d5125e1dab39028831a97e010585ef82b00b06bcdfbd316bf756c1b03</frbrgroupid><rsrctype>datasets</rsrctype><prefilter>datasets</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Medicine</topic><toplevel>online_resources</toplevel><creatorcontrib>Jungebluth, P.</creatorcontrib><creatorcontrib>Holzgraefe, B.</creatorcontrib><creatorcontrib>Lim, M.L.</creatorcontrib><creatorcontrib>Duru, A.D.</creatorcontrib><creatorcontrib>Lundin, V.</creatorcontrib><creatorcontrib>Heldring, N.</creatorcontrib><creatorcontrib>Wiklander O.P.B.</creatorcontrib><creatorcontrib>Nordin, J.Z.</creatorcontrib><creatorcontrib>Chrobok, M.</creatorcontrib><creatorcontrib>Roderburg, C.</creatorcontrib><creatorcontrib>Sjöqvist, S.</creatorcontrib><creatorcontrib>Anderstam, B.</creatorcontrib><creatorcontrib>Beltrán Rodríguez, A.</creatorcontrib><creatorcontrib>Haag, J.C.</creatorcontrib><creatorcontrib>Gustafsson, Y.</creatorcontrib><creatorcontrib>Roddewig, K.G.</creatorcontrib><creatorcontrib>Jones, P.</creatorcontrib><creatorcontrib>Wood M.J.A.</creatorcontrib><creatorcontrib>Luedde T.J</creatorcontrib><creatorcontrib>Teixeira, A.I.</creatorcontrib><creatorcontrib>Hermanson, O.</creatorcontrib><creatorcontrib>Winqvist, O.</creatorcontrib><creatorcontrib>Kalzén, H.</creatorcontrib><creatorcontrib>El Andaloussi, S.</creatorcontrib><creatorcontrib>Alici, E.</creatorcontrib><creatorcontrib>Macchiarini, P.</creatorcontrib><collection>DataCite (Open Access)</collection><collection>DataCite</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Jungebluth, P.</au><au>Holzgraefe, B.</au><au>Lim, M.L.</au><au>Duru, A.D.</au><au>Lundin, V.</au><au>Heldring, N.</au><au>Wiklander O.P.B.</au><au>Nordin, J.Z.</au><au>Chrobok, M.</au><au>Roderburg, C.</au><au>Sjöqvist, S.</au><au>Anderstam, B.</au><au>Beltrán Rodríguez, A.</au><au>Haag, J.C.</au><au>Gustafsson, Y.</au><au>Roddewig, K.G.</au><au>Jones, P.</au><au>Wood M.J.A.</au><au>Luedde T.J</au><au>Teixeira, A.I.</au><au>Hermanson, O.</au><au>Winqvist, O.</au><au>Kalzén, H.</au><au>El Andaloussi, S.</au><au>Alici, E.</au><au>Macchiarini, P.</au><format>book</format><genre>unknown</genre><ristype>DATA</ristype><title>Supplementary Material for: Autologous Peripheral Blood Mononuclear Cells as Treatment in Refractory Acute Respiratory Distress Syndrome</title><date>2016-10-21</date><risdate>2016</risdate><abstract>Background: Acute respiratory distress syndrome (ARDS) is a devastating disorder. Despite enormous efforts in clinical research, effective treatment options are lacking, and mortality rates remain unacceptably high. Objectives: A male patient with severe ARDS showed no clinical improvement with conventional therapies. Hence, an emergent experimental intervention was performed. Methods: We performed intratracheal administration of autologous peripheral blood-derived mononuclear cells (PBMCs) and erythropoietin (EPO). Results: We found that after 2 days of initial PBMC/EPO application, lung function improved and extracorporeal membrane oxygenation (ECMO) support was reduced. Bronchoscopy and serum inflammatory markers revealed reduced inflammation. Additionally, serum concentration of miR-449a, b, c and miR-34a, a transient upregulation of E-cadherin and associated chromatin marks in PBMCs indicated airway epithelial differentiation. Extracellular vesicles from PBMCs demonstrated anti-inflammatory capacity in a TNF-a-mediated nuclear factor-κB in vitro assay. Despite improving respiratory function, the patient died of multisystem organ failure on day 38 of ECMO treatment. Conclusions: This case report provides initial encouraging evidence to use locally instilled PBMC/EPO for treatment of severe refractory ARDS. The observed clinical improvement may partially be due to the anti-inflammatory effects of PBMC/EPO to promote tissue regeneration. Further studies are needed for more in-depth understanding of the underlying mechanisms of in vivo regeneration.</abstract><pub>Karger Publishers</pub><doi>10.6084/m9.figshare.4047357</doi><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier DOI: 10.6084/m9.figshare.4047357
ispartof
issn
language eng
recordid cdi_datacite_primary_10_6084_m9_figshare_4047357
source DataCite
subjects Medicine
title Supplementary Material for: Autologous Peripheral Blood Mononuclear Cells as Treatment in Refractory Acute Respiratory Distress Syndrome
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-10T14%3A07%3A03IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-datacite_PQ8&rft_val_fmt=info:ofi/fmt:kev:mtx:book&rft.genre=unknown&rft.au=Jungebluth,%20P.&rft.date=2016-10-21&rft_id=info:doi/10.6084/m9.figshare.4047357&rft_dat=%3Cdatacite_PQ8%3E10_6084_m9_figshare_4047357%3C/datacite_PQ8%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true