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dc.contributor.authorSponaas, Anne-Marit
dc.contributor.authorNejati Moharrami, Neda
dc.contributor.authorFeyzi, Emadoldin
dc.contributor.authorStandal, Therese
dc.contributor.authorRustad, Even Holth
dc.contributor.authorWaage, Anders
dc.contributor.authorSundan, Anders
dc.date.accessioned2016-03-02T14:18:18Z
dc.date.accessioned2016-03-08T14:50:43Z
dc.date.available2016-03-02T14:18:18Z
dc.date.available2016-03-08T14:50:43Z
dc.date.issued2015
dc.identifier.citationPLoS ONE 2015, 10:e0139867(10)nb_NO
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/11250/2381827
dc.description.abstractIn this study we set out to investigate whether anti PDL1 or PD–1 treatment targeting the immune system could be used against multiple myeloma. DCs are important in regulating T cell responses against tumors. We therefore determined PDL1 and PDL2 expression on DC populations in bone marrow of patients with plasma cell disorders using multicolour Flow Cytometry. We specifically looked at CD141+ and CD141- myeloid and CD303+ plasmacytoid DC. The majority of plasma cells (PC) and DC subpopulations expressed PDL1, but the proportion of positive PDL1+ cells varied among patients. A correlation between the proportion of PDL1+ PC and CD141+ mDC was found, suggesting both cell types could down-regulate the anti-tumor T cell response.nb_NO
dc.language.isoengnb_NO
dc.publisherPublic Library of Sciencenb_NO
dc.titlePDL1 expression on plasma and dendritic cells in myeloma bone marrow suggests benefit of targeted anti PD1-PDL1 therapynb_NO
dc.typePeer reviewednb_NO
dc.typeJournal articleen_GB
dc.date.updated2016-03-02T14:18:18Z
dc.source.journalPLoS ONEnb_NO
dc.identifier.doi10.1371/journal.pone.0139867
dc.identifier.cristin1300134
dc.description.localcode© 2015 Sponaas et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.nb_NO


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