Evidence map›Paper›PMID 23269245›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2013

Transfer of CD8+ T cell memory using Bcl-2 as a marker.

Alexis Dunkle, Ivan Dzhagalov, Claire Gordy, You-Wen He

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

22 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Atomistic TCR-ligand interactions instruct memory T-cell differentiation.bioRxiv : the preprint server for biology · 2025
    Article
  3. Article
  4. Article
  5. Review
  6. Transcriptional rewiring in CD8Frontiers in immunology · 2024
    Review
  7. Delayed vaccine-induced CD8Journal for immunotherapy of cancer · 2023
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Aging of Antiviral CD8Journal of immunology (Baltimore, Md. : 1950) · 2019
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. 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

4 authors at 2 institutions in 1 country.

Alexis DunkleDepartment of Immunology, Duke University Medical Center, Durham, NC 27710, USA.
Ivan Dzhagalov
Claire Gordy
You-Wen He
Duke Medical Center · USDuke University Hospital · US

Funding

BcI-2 family in T lymphocyte homeostasisR01AI074754 · NIAID · DUKE UNIVERSITY · PI HE, YOU-WEN · 2009 to 2013
$1.9M
Autophagy in T lymphocyte functionR01AI074944 · NIAID · DUKE UNIVERSITY · PI HE, YOU-WEN · 2009 to 2013
$1.9M
NIAID NIH HHS AI074754NIAID NIH HHS R01 AI074754NIAID NIH HHS R01 AI074944
6 · The paper itself

Abstract

The processes that regulate T cell memory generation are important for therapeutic design and the immune response to disease. However, what allows a subset of effector T cells to survive the contraction period to become memory cells is incompletely understood. The Bcl-2 family is critical for T cell survival, and Bcl-2 has been proposed to be important for the survival of memory cells. However, previous studies have relied on double-knockout models, potentially skewing the role of Bcl-2, and the use of Bcl-2 as a marker in adoptive transfer experiments, a method required to confirm the memory potential of cell subsets, has not been possible because of the intracellular localization of the protein. In this study, we present a novel Bcl-2 reporter mouse model and, to our knowledge, show for the first time that a distinct subset of effector T cells, and also a subset within the CD127(hi)KLRG1(lo) memory precursor effector cell population, retains high Bcl-2 expression at the peak of the CD8(+) T cell response to Listeria monocytogenes. Furthermore, we show that Bcl-2 correlates with memory potential in adoptive transfer experiments using both total responding CD8(+) T cells and memory precursor effector cells. These results show that even within the memory precursor effector cell population, Bcl-2 confers a survival advantage in a subset of effector CD8(+) T cells that allows differentiation into memory cells and cement Bcl-2 as a critical factor for T cell memory.

Indexed as

Genes, bcl-2TransgenesAdoptive TransferAnimalsBacterial ProteinsCD8-Positive T-LymphocytesChromosomes, Artificial, BacterialGenes, ReporterHumansHybridomasImmunologic MemoryListeria monocytogenesListeriosisLuminescent ProteinsMiceMice, Inbred C57BLBacterial ProteinsLuminescent ProteinsOvalbuminProto-Oncogene Proteins c-bcl-2Recombinant Fusion Proteinsyellow fluorescent protein, Bacteria

Identifiers

PMID23269245
PMCPMC4366938
OpenAlexW2113119609

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.