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dc.rights.licenseopenen_US
dc.contributor.authorALLAIN-MAILLET, Sophie
dc.contributor.authorBOSSEBOEUF, Adrien
dc.contributor.authorMENNESSON, Nicolas
dc.contributor.authorBOSTOËN, Mégane
dc.contributor.authorDUFEU, Laura
dc.contributor.authorCHOI, Eun Ho
dc.contributor.authorCLEYRAT, Cédric
hal.structure.identifierBiologie des maladies cardiovasculaires = Biology of Cardiovascular Diseases
dc.contributor.authorMANSIER, Olivier
dc.contributor.authorLIPPERT, Eric
dc.contributor.authorLE BRIS, Yannick
dc.contributor.authorGOMBERT, Jean-Marc
dc.contributor.authorGIRODON, François
dc.contributor.authorPETTAZZONI, Magali
dc.contributor.authorBIGOT-CORBEL, Edith
dc.contributor.authorHERMOUET, Sylvie
dc.date.accessioned2021-02-02T11:27:32Z
dc.date.available2021-02-02T11:27:32Z
dc.date.issued2020-08-28
dc.identifier.issn2072-6694en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/26090
dc.description.abstractEnInflammatory cytokines play a major role in myeloproliferative neoplasms (MPNs) as regulators of the MPN clone and as mediators of clinical symptoms and complications. Firstly, we investigated the effect of V617F on 42 molecules linked to inflammation. For V617F-mutated patients, the V617F allele burden (%V617F) correlated with the levels of IL-1β, IL-1Rα, IP-10 and leptin in polycythemia vera (PV), and with IL-33 in ET; for all other molecules, no correlation was found. Cytokine production was also studied in the human megakaryocytic cell line UT-7. Wild-type UT-7 cells secreted 27/42 cytokines measured. UT-7 clones expressing 50% or 75% V617F were generated, in which the production of IL-1β, IP-10 and RANTES was increased; other cytokines were not affected. Secondly, we searched for causes of chronic inflammation in MPNs other than driver mutations. Since antigen-driven selection is increasingly implicated in the pathogenesis of blood malignancies, we investigated whether proinflammatory glucosylsphingosine (GlcSph) may play a role in MPNs. We report that 20% (15/75) of MPN patients presented with anti-GlcSph IgGs, distinguished by elevated levels of 11 cytokines. In summary, only IL-1β and IP-10 were linked to V617F both in patients and in UT-7 cells; other inflammation-linked cytokines in excess in MPNs were not. For subsets of MPN patients, a possible cause of inflammation may be auto-immunity against glucolipids.
dc.language.isoENen_US
dc.subjectarticle clinique
dc.subject.enmyeloproliferative neoplasms
dc.subject.eninflammation
dc.subject.enCALR exon 9 mutants; interleukin-1 (IL-1 )
dc.subject.encytokines
dc.subject.eninterleukin-1 (IL-1 )
dc.subject.enIL-1R ; IP-10
dc.subject.enleptin
dc.subject.enIL-33
dc.subject.enUT-7
dc.subject.enCRISPR technology
dc.subject.enantigenic stimulation
dc.subject.englucolipids
dc.subject.englucosylsphingosine (GlcSph)
dc.subject.enauto-immunity
dc.title.enAnti-Glucosylsphingosine Autoimmunity, JAK2V617F-Dependent Interleukin-1β and JAK2V617F-Independent Cytokines in Myeloproliferative Neoplasms.
dc.title.alternativeCancers (Basel)en_US
dc.typeArticle de revueen_US
dc.identifier.doi10.3390/cancers12092446en_US
dc.identifier.pubmed32872203en_US
bordeaux.journalCancersen_US
bordeaux.volume12en_US
bordeaux.hal.laboratoriesBiologie des maladies cardiovasculaires - U1034en_US
bordeaux.issue9en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.exportfalse
workflow.import.sourcepubmed
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Cancers&rft.date=2020-08-28&rft.volume=12&rft.issue=9&rft.eissn=2072-6694&rft.issn=2072-6694&rft.au=ALLAIN-MAILLET,%20Sophie&BOSSEBOEUF,%20Adrien&MENNESSON,%20Nicolas&BOSTO%C3%8BN,%20M%C3%A9gane&DUFEU,%20Laura&rft.genre=article


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