Evidence map›Paper›PMID 28385788›Full record

ReviewGenes & development2017

The making of a lymphocyte: the choice among disparate cell fates and the IKAROS enigma.

Katia Georgopoulos

Abstract readReview
In one paragraph

Review in Genes & development, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing 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

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

  1. Pooled it
  2. Article
  3. IKZF-associated inborn errors of immunity.Journal of human immunity · 2025
    Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. A new pipeline SPICE identifies novel JUN-IKZF1 composite elements.bioRxiv : the preprint server for biology · 2024
    Article
  9. AIOLOS-Associated Inborn Errors of Immunity.Journal of clinical immunology · 2024
    Review
  10. Article
  11. Biomedicines · 2024
    Review
  12. Ikaros is a principal regulator of AireScience immunology · 2023
    Article
  13. Impaired tissue homing by the Ikzf3Frontiers in immunology · 2023
    Article
  14. Generation of CD34Cells · 2022
    Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Antitumor Activity of the Novel BTK Inhibitor TG-1701 Is Associated with Disruption of Ikaros Signaling in Patients with B-cell Non-Hodgkin Lymphoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
    Article
  20. Identification of hub genes and transcription factors involved in periodontitis on the basis of multiple microarray analysis.Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology · 2021
    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

1 author.

Katia GeorgopoulosCutaneous Biology Research Center, Massachusetts General Hospital, Harvard Medical School, Charlestown, Massachusetts 02129, USA.

Funding

Role of IKAROS in the Biology and Therapy of High-Risk Precursor B-Cell LeukemiaR01CA190964 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI GEORGOPOULOS, KATIA, VAN ETTEN, RICHARD A. · 2015 to 2019
$2.7M
Ikaros-based epigenetic regulation of T cell leukemogenesisR01CA158006 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI GEORGOPOULOS, KATIA · 2012 to 2016
$2.0M
Epigenetic regulation of proinflammatory responses in the skinR01AR069132 · NIAMS · MASSACHUSETTS GENERAL HOSPITAL · PI GEORGOPOULOS, KATIA · 2016 to 2020
$1.8M
Ikaros regulation: study on hemo-lymphopoiesisR01CA162092 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI GEORGOPOULOS, KATIA · 2011 to 2015
$1.8M
Mechanisms of human pre-B cell differentiationR21AI124326 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI GEORGOPOULOS, KATIA · 2016 to 2017
$450k
Epigenetic regulation of epidermal homeostasisR01AR064390 · NIAMS · MASSACHUSETTS GENERAL HOSPITAL · PI GEORGOPOULOS, KATIA · 2013 to 2013
$337k
NCI NIH HHS R01 CA158006NCI NIH HHS R01 CA162092NCI NIH HHS R01 CA190964NIAID NIH HHS R21 AI124326NIAMS NIH HHS R01 AR064390NIAMS NIH HHS R01 AR069132
6 · The paper itself

Abstract

Lymphocyte differentiation is set to produce myriad immune effector cells with the ability to respond to multitudinous foreign substances. The uniqueness of this developmental system lies in not only the great diversity of cellular functions that it can generate but also the ability of its differentiation intermediates and mature effector cells to expand upon demand, thereby providing lifelong immunity. Surprisingly, the goals of this developmental system are met by a relatively small group of DNA-binding transcription factors that work in concert to control the timing and magnitude of gene expression and fulfill the demands for cellular specialization, expansion, and maintenance. The cellular and molecular mechanisms through which these lineage-promoting transcription factors operate have been a focus of basic research in immunology. The mechanisms of development discerned in this effort are guiding clinical research on disorders with an immune cell base. Here, I focus on IKAROS, one of the earliest regulators of lymphoid lineage identity and a guardian of lymphocyte homeostasis.

Indexed as

AnimalsCell DifferentiationCell LineageGene Expression Regulation, DevelopmentalHomeostasisHumansIkaros Transcription FactorLymphocytesTranscription FactorsIkaros Transcription FactorTranscription FactorsBALLchromatin regulationIKAROSlineage primingsuperenhancers

Identifiers

PMID28385788
PMCPMC5393059

What OpenQuestion holds

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LicenceCC BY-NC
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.