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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00006937naa a2200769 4500
001oai:DiVA.org:uu-265697
003SwePub
008151102s2015 | |||||||||||000 ||eng|
009oai:prod.swepub.kib.ki.se:132122757
024a https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-2656972 URI
024a https://doi.org/10.5966/sctm.2015-00212 DOI
024a http://kipublications.ki.se/Default.aspx?queryparsed=id:1321227572 URI
040 a (SwePub)uud (SwePub)ki
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Simonson, Oscar E.u Karolinska Inst, Dept Mol Med & Surg, Karolinska Univ Hosp, Stockholm, Sweden.;Karolinska Inst, Dept Cardiothorac Surg & Anesthesia, Karolinska Univ Hosp, Stockholm, Sweden.;Karolinska Inst, Dept Lab Med, Karolinska Univ Hosp, Stockholm, Sweden.4 aut
2451 0a In Vivo Effects of Mesenchymal Stromal Cells in Two Patients With Severe Acute Respiratory Distress Syndrome
264 c 2015-08-18
264 1b Oxford University Press (OUP),c 2015
338 a print2 rdacarrier
500 a De 2 första författarna delar förstaförfattarskapet.De 3 sista författarna delar sistaförfattarskapet.
520 a Mesenchymal stromal cells (MSCs) have been investigated as a treatment for various inflammatory diseases because of their immunomodulatory and reparative properties. However, many basic questions concerning their mechanisms of action after systemic infusion remain unanswered. We performed a detailed analysis of the immunomodulatory properties and proteomic profile of MSCs systemically administered to two patients with severe refractory acute respiratory distress syndrome (ARDS) on a compassionate use basis and attempted to correlate these with in vivo anti-inflammatory actions. Both patients received 2 x 10(6) cells per kilogram, and each subsequently improved with resolution of respiratory, hemodynamic, and multiorgan failure. In parallel, a decrease was seen in multiple pulmonary and systemic markers of inflammation, including epithelial apoptosis, alveolar-capillary fluid leakage, and proinflammatory cytokines, microRNAs, and chemokines. In vitro studies of the MSCs demonstrated a broad anti-inflammatory capacity, including suppression of T-cell responses and induction of regulatory phenotypes in T cells, monocytes, and neutrophils. Some of these in vitro potency assessments correlated with, and were relevant to, the observed in vivo actions. These experiences highlight both the mechanistic information that can be gained from clinical experience and the value of correlating in vitro potency assessments with clinical effects. The findings also suggest, but do not prove, a beneficial effect of lung protective strategies using adoptively transferred MSCs in ARDS. Appropriate randomized clinical trials are required to further assess any potential clinical efficacy and investigate the effects on in vivo inflammation. STEM CELLS TRANSLATIONAL MEDICINE 2015;4:1199-1213
650 7a MEDICIN OCH HÄLSOVETENSKAPx Medicinsk bioteknologix Medicinsk bioteknologi0 (SwePub)304012 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Medical Biotechnologyx Medical Biotechnology0 (SwePub)304012 hsv//eng
653 a Acute respiratory distress syndrome
653 a Pulmonary diseases
653 a Respiratory tract
653 a Stem cells
653 a Cell transplantation
653 a Bone marrow stromal cells
653 a Cellular therapy
653 a Clinical translation
700a Mougiakakos, Dimitriosu Univ Erlangen Nurnberg, Dept Internal Med Hematol & Oncol, D-91054 Erlangen, Germany.4 aut
700a Heldring, Ninau Karolinska Institutet4 aut
700a Bassi, Giuliou Univ Verona, Dept Med, Sect Hematol, Stem Cell Res Lab, I-37100 Verona, Italy.4 aut
700a Johansson, Henrik J.u Karolinska Institutet4 aut
700a Dalen, Magnusu Karolinska Institutet4 aut
700a Jitschin, Reginau Karolinska Inst, Dept Lab Med, Karolinska Univ Hosp, Stockholm, Sweden.4 aut
700a Rodin, Sergeyu Karolinska Institutet4 aut
700a Corbascio, Matthiasu Karolinska Institutet4 aut
700a El Andaloussi, Samiru Karolinska Institutet4 aut
700a Wiklander, Oscar P. B.u Karolinska Institutet4 aut
700a Nordin, Joel Z.u Karolinska Institutet4 aut
700a Skog, Johanu Exosome Diagnost Inc, New York, NY USA.4 aut
700a Romain, Charlotteu Exosome Diagnost Inc, New York, NY USA.4 aut
700a Koestler, Tinau Exosome Diagnost Inc, New York, NY USA.4 aut
700a Johansson Hellgren, Lailau Uppsala universitet,Thoraxkirurgi4 aut0 (Swepub:uu)lahel172
700a Schiller, Petteru Uppsala universitet,Thoraxkirurgi4 aut0 (Swepub:uu)pesch021
700a Joachimsson, Per-Olofu Uppsala universitet,Anestesiologi och intensivvård4 aut0 (Swepub:uu)pejoa103
700a Hägglund, Hansu Karolinska Institutet,Uppsala universitet,Hematologi,Univ Uppsala Hosp, Dept Hematol, Uppsala, Sweden.4 aut0 (Swepub:uu)hanha689
700a Mattsson, Mattiasu Uppsala universitet,Hematologi,Univ Uppsala Hosp, Dept Hematol, Uppsala, Sweden.4 aut0 (Swepub:uu)matma431
700a Lentio, Janne4 aut
700a Faridani, Omid R.u Ludwig Inst Canc Res, S-10401 Stockholm, Sweden.4 aut
700a Sandberg, Rickardu Karolinska Institutet4 aut
700a Korsgren, Olleu Uppsala universitet,Klinisk immunologi4 aut0 (Swepub:uu)ollekors
700a Krampera, Maurou Univ Verona, Dept Med, Sect Hematol, Stem Cell Res Lab, I-37100 Verona, Italy.4 aut
700a Weiss, Daniel J.u Univ Vermont, Dept Med, Hlth Sci Res Facil, Burlington, VT USA.4 aut
700a Grinnemo, Karl-Henriku Karolinska Inst, Dept Mol Med & Surg, Karolinska Univ Hosp, Stockholm, Sweden.;Karolinska Inst, Dept Cardiothorac Surg & Anesthesia, Karolinska Univ Hosp, Stockholm, Sweden.;Vaccine & Gene Therapy Inst Florida, Ctr Dis Aging, Port St Lucie, FL USA.4 aut
700a Le Blanc, Katarinau Karolinska Institutet4 aut
710a Karolinska Inst, Dept Mol Med & Surg, Karolinska Univ Hosp, Stockholm, Sweden.;Karolinska Inst, Dept Cardiothorac Surg & Anesthesia, Karolinska Univ Hosp, Stockholm, Sweden.;Karolinska Inst, Dept Lab Med, Karolinska Univ Hosp, Stockholm, Sweden.b Univ Erlangen Nurnberg, Dept Internal Med Hematol & Oncol, D-91054 Erlangen, Germany.4 org
773t Stem Cells Translational Medicined : Oxford University Press (OUP)g 4:10, s. 1199-1213q 4:10<1199-1213x 2157-6564x 2157-6580
856u https://stemcellsjournals.onlinelibrary.wiley.com/doi/pdfdirect/10.5966/sctm.2015-0021
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-265697
8564 8u https://doi.org/10.5966/sctm.2015-0021
8564 8u http://kipublications.ki.se/Default.aspx?queryparsed=id:132122757

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