Evidence map›Paper›PMID 32709897›Full record

ReviewCell research2020

Metabolic signaling in T cells.

Justin A Shyer, Richard A Flavell, Will Bailis

Erratum issuedOpen access · hybridAbstract readReview
In one paragraph

Review in Cell research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 219 papers.

0numbers the graph read from it
0cells of the map it votes in
219citing papers in PubMed
15.4field-weighted citation impact, top 1% 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

219 citing papers in PubMed, 319 citations in OpenAlex.

  1. Nature communications · 2024
    Trial
  2. Review
  3. Article
  4. European journal of nuclear medicine and molecular imaging · 2026
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Aging diminishes thymic output, reduces naive T cells, promotes memory T-cell accumulation, and impairs thymic regeneration.American journal of physiology. Regulatory, integrative and comparative physiology · 2026
    Article
  13. Review
  14. Review
  15. Article
  16. Pharmacologic DPP-4 inhibition promotes CD8bioRxiv : the preprint server for biology · 2026
    Article
  17. Review
  18. Article
  19. LAG-3Immunology · 2026
    Article
  20. CD8Nature · 2026
    Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 3 institutions in 1 country.

Justin A ShyerDepartment of Immunobiology, Yale School of Medicine, New Haven, CT, USA.
Richard A FlavellDepartment of Immunobiology, Yale School of Medicine, New Haven, CT, USA. richard.flavell@yale.edu.ORCID http://orcid.org/0000-0003-4461-0778
Will BailisPathology and Laboratory Medicine, Children's Hospital of Philadelphia, Philadelphia, PA, USA. bailisw@email.chop.edu.
Children's Hospital of Philadelphia · USHoward Hughes Medical Institute · USYale University · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
An in vivo CRISPR-Cas9 genetic screen in murine primary T cells to discover metabolic regulators of follicular B helper T (Tfh) cell differentiationR33AR073048 · NIAMS · YALE UNIVERSITY · PI CRAFT, JOSEPH EDGAR, FLAVELL, RICHARD A · 2019 to 2019
$418k
The biochemical basis of immune cell reprogramming: how cellular metabolism regulates epigenetic remodeling during T cell differentiationK22AI141758 · NIAID · CHILDREN'S HOSP OF PHILADELPHIA · PI BAILIS, WILL H. · 2019 to 2020
$270k
Metabolic Regulation of follicular B helper T (Tfh) cell developmentF31AI133855 · NIAID · YALE UNIVERSITY · PI SHYER, JUSTIN ANDREW · 2017 to 2018
$82k
Howard Hughes Medical InstituteNCATS NIH HHS UL1 TR001863NIAID NIH HHS F31 AI133855NIAID NIH HHS K22 AI141758NIAMS NIH HHS R33 AR073048
6 · The paper itself

Abstract

The maintenance of organismal homeostasis requires partitioning and transport of biochemical molecules between organ systems, their composite cells, and subcellular organelles. Although transcriptional programming undeniably defines the functional state of cells and tissues, underlying biochemical networks are intricately intertwined with transcriptional, translational, and post-translational regulation. Studies of the metabolic regulation of immunity have elegantly illustrated this phenomenon. The cells of the immune system interface with a diverse set of environmental conditions. Circulating immune cells perfuse peripheral organs in the blood and lymph, patrolling for pathogen invasion. Resident immune cells remain in tissues and play more newly appreciated roles in tissue homeostasis and immunity. Each of these cell populations interacts with unique and dynamic tissue environments, which vary greatly in biochemical composition. Furthermore, the effector response of immune cells to a diverse set of activating cues requires unique cellular adaptations to supply the requisite biochemical landscape. In this review, we examine the role of spatial partitioning of metabolic processes in immune function. We focus on studies of lymphocyte metabolism, with reference to the greater immunometabolism literature when appropriate to illustrate this concept.

Indexed as

Signal TransductionAnimalsGene Expression RegulationHumansLymphocyte ActivationMitochondriaModels, BiologicalT-Lymphocytes

Identifiers

PMID32709897
PMCPMC7395146
OpenAlexW3045298676

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.