Evidence map›Paper›PMID 36911729›Full record

ReviewFrontiers in immunology2023

NFκB signaling in T cell memory.

Mark A Daniels, Dezzarae Luera, Emma Teixeiro

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
8.9field-weighted citation impact, top 2% 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

30 citing papers in PubMed, 48 citations in OpenAlex.

  1. Trial
  2. Review
  3. Pathogenic role of MIF receptor (CD74) expressing T cells in inflammatory arthritis.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
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  5. Review
  6. Article
  7. Article
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  9. Article
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  11. Article
  12. Review
  13. Review
  14. Article
  15. Two-stage CD8Nature communications · 2025
    Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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

3 authors at 1 institution in 1 country.

Mark A DanielsDepartment of Molecular Microbiology and Immunology, School of Medicine, University of Missouri, Columbia, MO, United States.
Dezzarae LueraDepartment of Molecular Microbiology and Immunology, School of Medicine, University of Missouri, Columbia, MO, United States.
Emma TeixeiroDepartment of Molecular Microbiology and Immunology, School of Medicine, University of Missouri, Columbia, MO, United States.
University of Missouri · US

Funding

Human CD3epsilon co-potentiation to boost immunotherapyU01CA244314 · NCI · UNIVERSITY OF MISSOURI-COLUMBIA · PI GIL PAGES, DIANA · 2019 to 2024
$3.8M
IMSD: An Initiative to Maximize Student Development in Biomedical Research at MUT32GM135744 · NIGMS · UNIVERSITY OF MISSOURI-COLUMBIA · PI SCHRUM, ADAM G. · 2020 to 2025
$2.6M
TCR signal transduction in the regulation of T cell memoryR01AI110420 · NIAID · UNIVERSITY OF MISSOURI-COLUMBIA · PI TEIXEIRO, EMMA · 2015 to 2019
$1.8M
T cell signal transduction in the regulation of T cell memory in response to infectionR56AI110420 · NIAID · UNIVERSITY OF MISSOURI-COLUMBIA · PI TEIXEIRO, EMMA · 2021 to 2021
$260k
NCI NIH HHS U01 CA244314NIAID NIH HHS R01 AI110420NIAID NIH HHS R56 AI110420NIGMS NIH HHS T32 GM135744
6 · The paper itself

Abstract

Memory T cells play an essential role in protecting against infectious diseases and cancer and contribute to autoimmunity and transplant rejection. Understanding how they are generated and maintained in the context of infection or vaccination holds promise to improve current immune-based therapies. At the beginning of any immune response, naïve T cells are activated and differentiate into cells with effector function capabilities. In the context of infection, most of these cells die once the pathogenic antigen has been cleared. Only a few of them persist and differentiate into memory T cells. These memory T cells are essential to host immunity because they are long-lived and can perform effector functions immediately upon re-infection. How a cell becomes a memory T cell and continues being one for months and even years past the initial infection is still not fully understood. Recent reviews have thoroughly discussed the transcriptional, epigenomic, and metabolic mechanisms that govern T cell memory differentiation. Yet much less is known of how signaling pathways that are common circuitries of multiple environmental signals regulate T cell outcome and, precisely, T cell memory. The function of the NFκB signaling system is perhaps best understood in innate cells. Recent findings suggest that NFκB signaling plays an essential and unique role in generating and maintaining CD8 T cell memory. This review aims to summarize these findings and discuss the remaining questions in the field.

Indexed as

Immunologic MemoryMemory T CellsCell DifferentiationNF-kappa BSignal TransductionNF-kappa Benvironmental cuesimmunological memoryNFκB signalingprotective immunityT cell memory

Identifiers

PMID36911729
PMCPMC9998984
OpenAlexW4321789704

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.