Evidence map›Paper›PMID 23523350›Full record

ArticleCell reports2013

Bystander-activated memory CD8 T cells control early pathogen load in an innate-like, NKG2D-dependent manner.

Talyn Chu, Aaron J Tyznik, Sarah Roepke, Amy M Berkley, Amanda Woodward-Davis, Laura Pattacini, Michael J Bevan, Dietmar Zehn, Martin Prlic

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 128 papers.

0numbers the graph read from it
0cells of the map it votes in
128citing papers in PubMed
5.9field-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

128 citing papers in PubMed, 186 citations in OpenAlex.

  1. Article
  2. NKRInflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Tissue-resident memory CD8Nature reviews. Gastroenterology & hepatology · 2025
    Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. DAMP-ing IBD: Extinguish the Fire and Prevent Smoldering.Digestive diseases and sciences · 2025
    Review
  16. Bystander CD8Frontiers in immunology · 2025
    Article
  17. Article
  18. Review
  19. Article
  20. Review

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

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

9 authors at 5 institutions in 2 countries.

Talyn ChuVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Aaron J Tyznik
Sarah Roepke
Amy M Berkley
Amanda Woodward-Davis
Laura Pattacini
Michael J Bevan
Dietmar Zehn
Martin Prlic
Fred Hutch Cancer Center · USHoward Hughes Medical Institute · USLa Jolla Institute for Immunology · USSwiss Vaccine Research Institute · CHUniversity of Washington · US

Funding

CYTOTOXIC RESPONSE TO HISTOCOMPATIBILITY ANTIGENSR01AI019335 · NIAID · UNIVERSITY OF WASHINGTON · PI BEVAN, MICHAEL J · 1985 to 2012
$4.4M
CD8 Tau cell contraction and memory formationR00AI079159 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PRLIC, MARTIN · 2011 to 2012
$495k
CD8 Tau cell contraction and memory formationK99AI079159 · NIAID · UNIVERSITY OF WASHINGTON · PI PRLIC, MARTIN · 2009 to 2009
$90k
CYTOTOXIC RESPONSE TO HISTOCOMPATIBILITY ANTIGENSR37AI019335 · NIAID · UNIVERSITY OF WASHINGTON · PI BEVAN, MICHAEL J · 1988 to 1997
–
Howard Hughes Medical InstituteNIAID NIH HHS AI 019335NIAID NIH HHS AI 079159NIAID NIH HHS K99 AI079159NIAID NIH HHS R00 AI079159NIAID NIH HHS R01 AI019335
6 · The paper itself

Abstract

During an infection the antigen-nonspecific memory CD8 T cell compartment is not simply an inert pool of cells, but becomes activated and cytotoxic. It is unknown how these cells contribute to the clearance of an infection. We measured the strength of T cell receptor (TCR) signals that bystander-activated, cytotoxic CD8 T cells (BA-CTLs) receive in vivo and found evidence of limited TCR signaling. Given this marginal contribution of the TCR, we asked how BA-CTLs identify infected target cells. We show that target cells express NKG2D ligands following bacterial infection and demonstrate that BA-CTLs directly eliminate these target cells in an innate-like, NKG2D-dependent manner. Selective inhibition of BA-CTL-mediated killing led to a significant defect in pathogen clearance. Together, these data suggest an innate role for memory CD8 T cells in the early immune response before the onset of a de novo generated, antigen-specific CD8 T cell response.

Indexed as

Immunity, InnateImmunologic MemoryLymphocyte ActivationAnimalsBacterial LoadCD8-Positive T-LymphocytesMiceMice, Inbred C57BLNK Cell Lectin-Like Receptor Subfamily KReceptors, Antigen, T-CellKlrk1 protein, mouseNK Cell Lectin-Like Receptor Subfamily KReceptors, Antigen, T-Cell

Identifiers

PMID23523350
PMCPMC3628815
OpenAlexW2052558938

What OpenQuestion holds

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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.