Evidence map›Paper›PMID 31263277›Full record

ArticleNature immunology2019

Epigenetic programming underpins B cell dysfunction in human SLE.

Christopher D Scharer, Emily L Blalock, Tian Mi, Benjamin G Barwick, Scott A Jenks, Tsuneo Deguchi, Kevin S Cashman, Bridget E Neary, Dillon G Patterson, Sakeenah L Hicks and 5 more

Abstract read
In one paragraph

Article in Nature immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 108 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
108citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

108 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Defective B cell tolerance in SLE lymph nodes underpins VHmedRxiv : the preprint server for health sciences · 2026
    Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. IL-4 alters TLR7-induced B cell developmental program in lupus.Clinical immunology (Orlando, Fla.) · 2025
    Article
  19. Article
  20. Review

48 more citing papers are in PubMed but not listed here.

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

15 authors.

Christopher D ScharerDepartment of Microbiology and Immunology, School of Medicine, Emory University, Atlanta, GA, USA.ORCID http://orcid.org/0000-0001-7716-8504
Emily L BlalockDivision of Rheumatology, Department of Medicine, School of Medicine, Emory University, Atlanta, GA, USA.
Tian MiDepartment of Microbiology and Immunology, School of Medicine, Emory University, Atlanta, GA, USA.
Benjamin G BarwickDepartment of Hematology and Medical Oncology, School of Medicine, Emory University, Atlanta, GA, USA.ORCID http://orcid.org/0000-0001-9810-3566
Scott A JenksDivision of Rheumatology, Department of Medicine, School of Medicine, Emory University, Atlanta, GA, USA.
Tsuneo DeguchiDivision of Rheumatology, Department of Medicine, School of Medicine, Emory University, Atlanta, GA, USA.
Kevin S CashmanDivision of Rheumatology, Department of Medicine, School of Medicine, Emory University, Atlanta, GA, USA.
Bridget E NearyDivision of Rheumatology, Department of Medicine, School of Medicine, Emory University, Atlanta, GA, USA.
Dillon G PattersonDepartment of Microbiology and Immunology, School of Medicine, Emory University, Atlanta, GA, USA.
Sakeenah L HicksDepartment of Microbiology and Immunology, School of Medicine, Emory University, Atlanta, GA, USA.
Arezou KhosroshahiDivision of Rheumatology, Department of Medicine, School of Medicine, Emory University, Atlanta, GA, USA.
F Eun-Hyung LeeLowance Center for Human Immunology, School of Medicine, Emory University, Atlanta, GA, USA.
Chungwen WeiDivision of Rheumatology, Department of Medicine, School of Medicine, Emory University, Atlanta, GA, USA.ORCID http://orcid.org/0000-0001-5457-6919
Iñaki SanzDivision of Rheumatology, Department of Medicine, School of Medicine, Emory University, Atlanta, GA, USA. ignacio.sanz@emory.edu.
Jeremy M BossDepartment of Microbiology and Immunology, School of Medicine, Emory University, Atlanta, GA, USA. jmboss@emory.edu.ORCID http://orcid.org/0000-0002-2432-1840

Funding

Regulation of B cell Responses in SLE and Other Autoimmune DiseasesU19AI110483 · NIAID · EMORY UNIVERSITY · PI Ignacio E. Sanz · 2014 to 2026
$76.6M
Regulation of Pathogenic Plasma Cells in Human SLEP01AI125180 · NIAID · EMORY UNIVERSITY · PI Ignacio E. Sanz · 2016 to 2026
$28.2M
Virus-induced Cell Fate Decisions in Anti-Viral ImmunityU19AI109962 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI LUND, FRANCES E. · 2014 to 2018
$11.6M
PREDOCTORAL TRAINING PROGRAM IN GENETICST32GM008490 · NIGMS · EMORY UNIVERSITY · PI BOSS, JEREMY M. · 1993 to 2022
$8.0M
Molecular Mechanisms of Human Long-lived Plasma Cell Generation in the Bone Marrow and SpleenU01AI141993 · NIAID · EMORY UNIVERSITY · PI Frances Eun-Hyung Lee · 2019 to 2026
$5.7M
Regulation of PD-1 gene expressionR01AI113021 · NIAID · EMORY UNIVERSITY · PI BOSS, JEREMY M. · 2014 to 2024
$4.7M
A Model System for the Study of Human B-cell ToleranceR37AI049660 · NIAID · UNIVERSITY OF ROCHESTER · PI SANZ, IGNACIO E. · 2010 to 2019
$3.7M
Understanding Survival of Human Bone Marrow Long-Lived Plasma CellsR01AI121252 · NIAID · EMORY UNIVERSITY · PI LEE, FRANCES EUN-HYUNG · 2016 to 2020
$2.7M
Epigenetic Regulation of Plasma Cells DifferentiationR01AI123733 · NIAID · EMORY UNIVERSITY · PI BOSS, JEREMY M. · 2016 to 2020
$1.9M
Epigenetic Programming of B cell Terminal DifferentiationF31AI112261 · NIAID · EMORY UNIVERSITY · PI BARWICK, BENJAMIN GABRIEL · 2014 to 2016
$120k
NIAID NIH HHS F31 AI112261NIAID NIH HHS P01 AI125180NIAID NIH HHS R01 AI113021NIAID NIH HHS R01 AI121252NIAID NIH HHS R01 AI123733NIAID NIH HHS R37 AI049660NIAID NIH HHS U01 AI141993NIAID NIH HHS U19 AI109962NIAID NIH HHS U19 AI110483NIGMS NIH HHS T32 GM008490
6 · The paper itself

Abstract

Systemic lupus erythematosus (SLE) is characterized by the expansion of extrafollicular pathogenic B cells derived from newly activated naive cells. Although these cells express distinct markers, their epigenetic architecture and how it contributes to SLE remain poorly understood. To address this, we determined the DNA methylomes, chromatin accessibility profiles and transcriptomes from five human B cell subsets, including a newly defined effector B cell subset, from subjects with SLE and healthy controls. Our data define a differentiation hierarchy for the subsets and elucidate the epigenetic and transcriptional differences between effector and memory B cells. Importantly, an SLE molecular signature was already established in resting naive cells and was dominated by enrichment of accessible chromatin in motifs for AP-1 and EGR transcription factors. Together, these factors acted in synergy with T-BET to shape the epigenome of expanded SLE effector B cell subsets. Thus, our data define the molecular foundation of pathogenic B cell dysfunction in SLE.

Indexed as

B-Lymphocyte SubsetsChromatin Assembly and DisassemblyDNA MethylationEarly Growth Response Transcription FactorsEpigenesis, GeneticHumansLupus Erythematosus, SystemicTranscription Factor AP-1TranscriptomeEarly Growth Response Transcription FactorsTranscription Factor AP-1

Identifiers

PMID31263277
PMCPMC6642679

What OpenQuestion holds

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Read underepoch 390

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.