Evidence map›Paper›PMID 34010461›Full record

ReviewImmunological reviews2021

Epigenetic gene regulation in plasma cells.

Dillon G Patterson, Anna K Kania, Zhihong Zuo, Christopher D Scharer, Jeremy M Boss

Open access · greenAbstract readReview
In one paragraph

Review in Immunological reviews, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

14 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. H3K27me3 Demethylase UTX Restrains Plasma Cell Formation.Journal of immunology (Baltimore, Md. : 1950) · 2022
    Article
  12. Article
  13. Article
  14. Article
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

5 authors at 2 institutions in 2 countries.

Dillon G PattersonDepartment of Microbiology and Immunology, Emory University, Atlanta, GA, USA.ORCID 0000-0001-6053-5216
Anna K KaniaDepartment of Microbiology and Immunology, Emory University, Atlanta, GA, USA.ORCID 0000-0002-5819-5694
Zhihong ZuoDepartment of Microbiology and Immunology, Emory University, Atlanta, GA, USA.
Christopher D ScharerDepartment of Microbiology and Immunology, Emory University, Atlanta, GA, USA.ORCID 0000-0001-7716-8504
Jeremy M BossDepartment of Microbiology and Immunology, Emory University, Atlanta, GA, USA.ORCID 0000-0002-2432-1840
Emory University · USCentral South University · CN

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
PREDOCTORAL TRAINING PROGRAM IN GENETICST32GM008490 · NIGMS · EMORY UNIVERSITY · PI BOSS, JEREMY M. · 1993 to 2022
$8.0M
Role of the DR/DQ super enhancer in MHC-II expressionR01AI153102 · NIAID · EMORY UNIVERSITY · PI BOSS, JEREMY M. · 2020 to 2024
$2.4M
Epigenetic instruction of memory B cell function and reactivationR01AI148471 · NIAID · EMORY UNIVERSITY · PI SCHARER, CHRISTOPHER D · 2020 to 2024
$1.9M
Epigenetic Regulation of Plasma Cells DifferentiationR01AI123733 · NIAID · EMORY UNIVERSITY · PI BOSS, JEREMY M. · 2016 to 2020
$1.9M
NIAID NIH HHS P01 AI125180NIAID NIH HHS R01 AI123733NIAID NIH HHS R01 AI148471NIAID NIH HHS R01 AI153102NIAID NIH HHS U19 AI110483NIGMS NIH HHS T32 GM008490
6 · The paper itself

Abstract

Humoral immunity provides protection from pathogenic infection and is mediated by antibodies following the differentiation of naive B cells (nBs) to antibody-secreting cells (ASCs). This process requires substantial epigenetic and transcriptional rewiring to ultimately repress the nB program and replace it with one conducive to ASC physiology and function. Notably, these reprogramming events occur within the framework of cell division. Efforts to understand the relationship of cell division with reprogramming and ASC differentiation in vivo have uncovered the timing and scope of reprogramming, as well as key factors that influence these events. Herein, we discuss the unique physiology of ASC and how nBs undergo epigenetic and genome architectural reorganization to acquire the necessary functions to support antibody production. We also discuss the stage-wise manner in which reprogramming occurs across cell divisions and how key molecular determinants can influence B cell fate outcomes.

Indexed as

Antibody-Producing CellsPlasma CellsB-LymphocytesCell DifferentiationEpigenesis, GeneticGene Expression RegulationB cell differentiationcell divisionepigeneticshemeplasma cellstranscriptomics

Identifiers

PMID34010461
PMCPMC8387415
OpenAlexW3160371754

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.