Evidence map›Paper›PMID 19879163›Full record

ArticleImmunity2009

A distinct subset of self-renewing human memory CD8+ T cells survives cytotoxic chemotherapy.

Cameron J Turtle, Hillary M Swanson, Nobuharu Fujii, Elihu H Estey, Stanley R Riddell

Open access · bronzeAbstract read
In one paragraph

Article in Immunity, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 110 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
110citing papers in PubMed, 1 pooled it
5.8field-weighted citation impact, top 3% 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

110 citing papers in PubMed, 1 synthesis or guideline pooled it, 176 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
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  5. Interleukin-18 armours antitumour immune effectors.Nature reviews. Immunology · 2026
    Review
  6. Clinical significance of CD161Journal for immunotherapy of cancer · 2026
    Article
  7. Article
  8. Review
  9. Article
  10. Article
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  12. Article
  13. Platinum-Based Chemotherapy Attenuates the Effector Response of CD8 T Cells to Concomitant PD-1 Blockade.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Article
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  15. Article
  16. Review
  17. Review
  18. Article
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50 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 2 countries.

Cameron J TurtleProgram in Immunology, Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA. cturtle@fhcrc.org
Hillary M Swanson
Nobuharu Fujii
Elihu H Estey
Stanley R Riddell
Fred Hutch Cancer Center · USUniversity of Washington · USCape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa · ZA

Funding

VIRUS-MEDIATED MYELOSUPPRESSIONP01CA018029 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Geoffrey Roger HILL · 1985 to 2026
$128.4M
TARGETING ROR1 WITH CHIMERIC ANTIGEN RECEPTOR MODIFIED T CELLSR01CA114536 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Sylvain Simon · 2005 to 2026
$8.4M
CD8+ T Cell Immunity to CytomegalovirusR01AI053193 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI RIDDELL, STANLEY R. · 2003 to 2013
$4.6M
NCI NIH HHS CA114536NCI NIH HHS CA18029NCI NIH HHS P01 CA018029NCI NIH HHS R01 CA114536NIAID NIH HHS AI53193NIAID NIH HHS R01 AI053193
6 · The paper itself

Abstract

The mechanisms that maintain human T cell memory during normal and perturbed homeostasis are not fully understood. The repeated induction of profound lymphocytopenia in patients undergoing multiple cycles of cytotoxic chemotherapy infrequently results in severe infections with viruses controlled by memory T cells, suggesting that some memory T cells survive chemotherapy and restore immunity. Here, we identified a distinct subpopulation of memory CD8(+) T cells with the ability to rapidly efflux and survive exposure to chemotherapy drugs in vitro and in vivo. T cells with high efflux capacity shared expression of molecules with hematopoietic stem cells, were quiescent in nonlymphocytopenic individuals, and were induced to proliferate in patients rendered lymphocytopenic after chemotherapy. Effluxing T cells differentiated into noneffluxing subsets in response to antigen stimulation and inflammatory signals, thereby contributing to repopulation of memory cells after chemotherapy.

Indexed as

Cytotoxicity, ImmunologicImmunologic MemoryAntibiotics, AntineoplasticCD8-Positive T-LymphocytesCell ProliferationDaunorubicinDown-RegulationHomeostasisHumansIdarubicinLymphocyte ActivationT-Lymphocyte SubsetsAntibiotics, AntineoplasticDaunorubicinIdarubicin

Identifiers

PMID19879163
PMCPMC2789980
OpenAlexW2036378796

What OpenQuestion holds

Textmetadata
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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.