Evidence map›Paper›PMID 27097762›Full record

ArticleNature communications2016

Virtual memory T cells develop and mediate bystander protective immunity in an IL-15-dependent manner.

Jason T White, Eric W Cross, Matthew A Burchill, Thomas Danhorn, Martin D McCarter, Hugo R Rosen, Brian O'Connor, Ross M Kedl

Abstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 154 papers.

0numbers the graph read from it
0cells of the map it votes in
154citing papers in PubMed
–field-weighted citation impact
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

154 citing papers in PubMed.

  1. Article
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  9. Cytotoxic CD4Signal transduction and targeted therapy · 2026
    Review
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  15. Article
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94 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

8 authors.

Jason T WhiteDepartment of Immunology and Microbiology, University of Colorado Denver at Anschutz Medical Campus, School of Medicine, Aurora, Colorado 80045, USA.
Eric W CrossDepartment of Immunology and Microbiology, University of Colorado Denver at Anschutz Medical Campus, School of Medicine, Aurora, Colorado 80045, USA.
Matthew A BurchillDepartment of Medicine and Division of Gastroenterology and Hepatology, University of Colorado Denver at Anschutz Medical Campus, School of Medicine, Aurora, Colorado 80045, USA.
Thomas DanhornDepartment of Biomedical Research, National Jewish Health, Denver, Colorado 80206, USA.ORCID http://orcid.org/0000-0002-3861-8602
Martin D McCarterDepartment of Surgery, University of Colorado Denver at Anschutz Medical Campus, School of Medicine, Aurora, Colorado 80045, USA.
Hugo R RosenDepartment of Medicine and Division of Gastroenterology and Hepatology, University of Colorado Denver at Anschutz Medical Campus, School of Medicine, Aurora, Colorado 80045, USA.
Brian O'ConnorDepartment of Biomedical Research, National Jewish Health, Denver, Colorado 80206, USA.
Ross M KedlDepartment of Immunology and Microbiology, University of Colorado Denver at Anschutz Medical Campus, School of Medicine, Aurora, Colorado 80045, USA.

Funding

Medical Scientist Training ProgramT32GM008497 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI WILSON, CARA C. · 1993 to 2022
$15.2M
Transcriptional regulation of vaccine-elicited and infection-elicited CD8+ T cell responsesR01AI066121 · NIAID · UNIVERSITY OF COLORADO DENVER · PI Ross M Kedl · 2007 to 2026
$7.1M
Virtual Memory T Cell Development and Responses In VivoR01AI101205 · NIAID · UNIVERSITY OF COLORADO DENVER · PI KEDL, ROSS M · 2013 to 2017
$1.8M
NIAID NIH HHS R01 AI066121NIAID NIH HHS R01 AI101205NIGMS NIH HHS T32 GM008497
6 · The paper itself

Abstract

Virtual memory cells (VM) are an antigen-specific, memory phenotype CD8 T-cell subset found in lymphoreplete, unchallenged mice. Previous studies indicated that VM cells were the result of homeostatic proliferation (HP) resembling the proliferation observed in a lymphopenic environment. Here we demonstrate that HP is ongoing in lymphoreplete mice, the degree of which is dictated by the number of naive CD8 T cells with a sufficiently high affinity for self-antigen interacting with peripheral IL-15. VM cell transcriptional profiles suggest a capacity to mediate protective immunity via antigen non-specific bystander killing, a function we show is dependent on IL-15. Finally, we show a VM-like population of human cells that accumulate with age and traffic to the liver, displaying phenotypic and functional attributes consistent with the bystander protective functions of VM cells identified in the mouse. These data identify developmental and functional attributes of VM cells, including their likely role in protective immunity.

Indexed as

Immunity, InnateImmunologic MemoryAdultAgedAnimalsAutoantigensBystander EffectCD8-Positive T-LymphocytesCell MovementCell ProliferationFemaleGene ExpressionHomeostasisHumansInterleukin-15LiverAutoantigensInterleukin-15

Identifiers

PMID27097762
PMCPMC4844673

What OpenQuestion holds

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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.