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High proportion of anergic B cells in the bone marrow defined phenotypically by CD21(-/low)/CD38- expression predicts poor survival in diffuse large B cell lymphoma

dc.contributor.authorRijal, Sewa
dc.contributor.authorKok, Johanna
dc.contributor.authorCoombes, Caitlin
dc.contributor.authorSmyth, Lillian
dc.contributor.authorHourigan, Jayde
dc.contributor.authorJain, Sanjiv
dc.contributor.authorTalaulikar, Dipti
dc.date.accessioned2023-12-12T23:26:20Z
dc.date.available2023-12-12T23:26:20Z
dc.date.issued2020
dc.date.updated2022-09-11T08:16:32Z
dc.description.abstractBackground Diffuse large B cell lymphoma (DLBCL) is the commonest lymphoma that is highly aggressive where one-third of the patients relapse despite effective treatment. Interaction between the lymphoma cells and the non-clonal immune cells within the bone marrow microenvironment is thought to play a critical role in the pathogenesis of DLBCL. Methods We used flow cytometry to characterize the proportion of B cell subpopulations in the bone marrow (N = 47) and peripheral blood (N = 54) of 75 DLBCL patients at diagnosis and study their impact on survival. Results Anergic B cells in the bone marrow (BM), characterized as having CD21(−/low)/CD38- expression, influenced survival with high numbers (defined as > 13.9%) being associated with significantly shorter overall survival (59.7 months vs 113.6 months, p = 0.0038). Interestingly, low numbers of anergic B cells in the BM (defined as ≤13.9%) was associated with germinal center B cell type of DLBCL (p = 0.0354) that is known to have superior rates of survival when compared to activated B cell type. Finally, Cox regression analysis in our cohort of patients established that the inferior prognosis of having high numbers of anergic B cells in the bone marrow was independent of the established Revised International Prognostic Index (R-IPI) score. Conclusions High proportion of anergic B cells in the BM characterized by CD21(−/low)/CD38- expression predicts poor survival outcomes in DLBCL.en_AU
dc.description.sponsorshipThe Canberra Hospital private trust fund.en_AU
dc.format.mimetypeapplication/pdfen_AU
dc.identifier.issn1471-2407en_AU
dc.identifier.urihttp://hdl.handle.net/1885/309833
dc.language.isoen_AUen_AU
dc.provenanceThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.en_AU
dc.publisherBioMed Centralen_AU
dc.rights© 2020 The authorsen_AU
dc.rights.licenseCreative Commons Attribution licenceen_AU
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_AU
dc.sourceBMC Canceren_AU
dc.subjectDiffuse large B cell lymphomaen_AU
dc.subjectB cellsen_AU
dc.subjectPrognosisen_AU
dc.subjectMicroenvironmenten_AU
dc.subjectAnergicen_AU
dc.titleHigh proportion of anergic B cells in the bone marrow defined phenotypically by CD21(-/low)/CD38- expression predicts poor survival in diffuse large B cell lymphomaen_AU
dc.typeJournal articleen_AU
dcterms.accessRightsOpen Accessen_AU
local.bibliographicCitation.issue1en_AU
local.bibliographicCitation.lastpage9en_AU
local.bibliographicCitation.startpage1en_AU
local.contributor.affiliationRijal, Sewa, College of Health and Medicine, ANUen_AU
local.contributor.affiliationKok, Johanna, Canberra Hospitalen_AU
local.contributor.affiliationCoombes, Caitlin, College of Health and Medicine, ANUen_AU
local.contributor.affiliationSmyth, Lillian, College of Health and Medicine, ANUen_AU
local.contributor.affiliationHourigan, Jayde, Canberra Hospitalen_AU
local.contributor.affiliationJain, Sanjiv, Canberra Hospitalen_AU
local.contributor.affiliationTalaulikar, Dipti, College of Health and Medicine, ANUen_AU
local.contributor.authoruidRijal, Sewa, u6366126en_AU
local.contributor.authoruidCoombes, Caitlin, u4520019en_AU
local.contributor.authoruidSmyth, Lillian, u4210896en_AU
local.contributor.authoruidTalaulikar, Dipti, u4283279en_AU
local.description.notesImported from ARIESen_AU
local.identifier.absfor321100 - Oncology and carcinogenesisen_AU
local.identifier.absfor320100 - Cardiovascular medicine and haematologyen_AU
local.identifier.ariespublicationa383154xPUB14534en_AU
local.identifier.citationvolume20en_AU
local.identifier.doi10.1186/s12885-020-07525-6en_AU
local.identifier.thomsonIDWOS:000590594500007
local.type.statusPublished Versionen_AU

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