Evidence map›Paper›PMID 19269192›Full record

ReviewSeminars in immunology2009

Surviving the crash: transitioning from effector to memory CD8+ T cell.

Louise M D'Cruz, Mark P Rubinstein, Ananda W Goldrath

Open access · greenAbstract readReview
In one paragraph

Review in Seminars in immunology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

53 citing papers in PubMed, 89 citations in OpenAlex.

  1. Review
  2. Cytotoxic T Cells: Kill, Memorize, and Mask to Maintain Immune Homeostasis.International journal of molecular sciences · 2025
    Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Themis suppresses the effector function of CD8Cellular & molecular immunology · 2023
    Article
  8. Article
  9. Article
  10. BATF3 programs CD8Nature immunology · 2020
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. IL-2 and Beyond in Cancer Immunotherapy.Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research · 2018
    Review
  17. Article
  18. Understanding memory CD8Immunology letters · 2017
    Review
  19. Targeting Angiotensin II Type-1 Receptor (ATFrontiers in cellular and infection microbiology · 2017
    Article
  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.

Louise M D'CruzUniversity of California San Diego, Division of Biological Sciences, 9500 Gilman Drive, La Jolla, CA 92093-0377, United States.
Mark P Rubinstein
Ananda W Goldrath
University of California, San Diego · US

Funding

T cell maintenance: molecular mediators of the TCR-derived survival signalR01AI067545 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GOLDRATH, ANANDA W · 2006 to 2021
$6.1M
Regulation of T cell immunity to viral infectionR01AI072117 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GOLDRATH, ANANDA W · 2008 to 2022
$5.4M
T cell maintenance: molecular mediators of T cell differentiation and survivalR37AI067545 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Ananda W Goldrath · 2022 to 2026
$3.0M
NIAID NIH HHS R01 AI067545NIAID NIH HHS R01 AI072117NIAID NIH HHS R37 AI067545
6 · The paper itself

Abstract

One outcome of infection is the formation of long-lived immunological memory, which provides durable protection from symptomatic re-infection. In response to infection or vaccination, T cells undergo dramatic proliferation and differentiate into effector T cells that mediate removal of the pathogen. Following pathogen clearance, the majority of effector cells die, restoring lymphocyte homeostasis. However, a small number of antigen-specific cells survive and seed the memory T cell population. Here, we focus on recent advances in identifying the key proteins and transcription factors that allow a portion of effector CD8(+) T cells to persist after contraction of the immune response, forming a memory cell population programmed for long-term self-renewal and survival. We also examine new findings addressing the role of environmental cues such as cytokines and co-stimulatory molecules in CD8(+) memory T cell formation and how the cell-extrinsic cues influence the molecular players of intracellular pathways important for memory formation.

Indexed as

Cytotoxicity, ImmunologicImmunologic MemoryAnimalsApoptosisCD8-Positive T-LymphocytesCell DifferentiationCytokinesDNA-Binding ProteinsHumansInfectionsInhibitor of Differentiation Protein 2Positive Regulatory Domain I-Binding Factor 1Proto-Oncogene Proteins c-bcl-6Repressor ProteinsSignal TransductionT-bet Transcription FactorBCL6 protein, humanCytokinesDNA-Binding ProteinsEOMES protein, humanID2 protein, humanInhibitor of Differentiation Protein 2Positive Regulatory Domain I-Binding Factor 1PRDM1 protein, humanProto-Oncogene Proteins c-bcl-6Repressor ProteinsT-bet Transcription FactorT-Box Domain Proteins

Identifiers

PMID19269192
PMCPMC2671236
OpenAlexW1973390559

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.