Evidence map›Paper›PMID 33143694›Full record

ArticleBMC cancer2020

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.

Sewa Rijal, Johanna Kok, Caitlin Coombes, Lillian Smyth, Jayde Hourigan, Sanjiv Jain, Dipti Talaulikar

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 41% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Diverging in Vivo Immune Response Patterns After Oral Food Challenge in Peanut Allergic Adults.Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 2026
    Article
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  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Sewa RijalAustralian National University Medical School, College of Medicine, Biology and Environment, Canberra, Australia.
Johanna KokHaematology Translational Research Unit, Department of Hematology, Canberra Hospital, Canberra, Australia.
Caitlin CoombesAustralian National University Medical School, College of Medicine, Biology and Environment, Canberra, Australia.
Lillian SmythAustralian National University Medical School, College of Medicine, Biology and Environment, Canberra, Australia.
Jayde HouriganDepartment of Diagnostic Genomics, Canberra Hospital, Canberra, Australia.
Sanjiv JainDepartment of Anatomical Pathology, Canberra Hospital, Canberra, Australia.
Dipti TalaulikarAustralian National University Medical School, College of Medicine, Biology and Environment, Canberra, Australia. dipti.talaulikar@act.gov.au.ORCID http://orcid.org/0000-0001-6766-8345
Australian National University · AUCanberra Hospital · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDiffuse 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.

methodsWe 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.

resultsAnergic 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.

conclusionsHigh proportion of anergic B cells in the BM characterized by CD21(-/low)/CD38- expression predicts poor survival outcomes in DLBCL.

Indexed as

ADP-ribosyl Cyclase 1AdultAgedAged, 80 and overB-LymphocytesBone MarrowClonal AnergyDown-RegulationFemaleFlow CytometryHumansLymphoma, Large B-Cell, DiffuseMaleMembrane GlycoproteinsMiddle AgedPrognosisADP-ribosyl Cyclase 1CD38 protein, humanMembrane GlycoproteinsReceptors, Complement 3dAnergicB cellsDiffuse large B cell lymphomaMicroenvironmentPrognosis

Identifiers

PMID33143694
PMCPMC7641859
OpenAlexW3096599121

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.