Evidence map›Paper›PMID 31083700›Full record

ArticlePLoS pathogens2019

Early primed KLRG1- CMV-specific T cells determine the size of the inflationary T cell pool.

Nicolas S Baumann, Suzanne P M Welten, Nicole Torti, Katharina Pallmer, Mariana Borsa, Isabel Barnstorf, Jennifer D Oduro, Luka Cicin-Sain, Annette Oxenius

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

16 citing papers in PubMed, 25 citations in OpenAlex.

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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 2 institutions in 2 countries.

Nicolas S BaumannInstitute of Microbiology, ETH Zürich, Vladimir-Prelog-Weg 4, Zürich, Switzerland.
Suzanne P M WeltenInstitute of Microbiology, ETH Zürich, Vladimir-Prelog-Weg 4, Zürich, Switzerland.
Nicole TortiInstitute of Microbiology, ETH Zürich, Vladimir-Prelog-Weg 4, Zürich, Switzerland.
Katharina PallmerInstitute of Microbiology, ETH Zürich, Vladimir-Prelog-Weg 4, Zürich, Switzerland.ORCID 0000-0003-2009-9354
Mariana BorsaInstitute of Microbiology, ETH Zürich, Vladimir-Prelog-Weg 4, Zürich, Switzerland.
Isabel BarnstorfInstitute of Microbiology, ETH Zürich, Vladimir-Prelog-Weg 4, Zürich, Switzerland.
Jennifer D OduroDepartment of Vaccinology and Applied Microbiology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Luka Cicin-SainDepartment of Vaccinology and Applied Microbiology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Annette OxeniusInstitute of Microbiology, ETH Zürich, Vladimir-Prelog-Weg 4, Zürich, Switzerland.ORCID 0000-0002-2079-2354
ETH Zurich · CHHelmholtz Centre for Infection Research · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Memory T cell inflation is a process in which a subset of cytomegalovirus (CMV) specific CD8 T cells continuously expands mainly during latent infection and establishes a large and stable population of effector memory cells in peripheral tissues. Here we set out to identify in vivo parameters that promote and limit CD8 T cell inflation in the context of MCMV infection. We found that the inflationary T cell pool comprised mainly high avidity CD8 T cells, outcompeting lower avidity CD8 T cells. Furthermore, the size of the inflationary T cell pool was not restricted by the availability of specific tissue niches, but it was directly related to the number of virus-specific CD8 T cells that were activated during priming. In particular, the amount of early-primed KLRG1- cells and the number of inflationary cells with a central memory phenotype were a critical determinant for the overall magnitude of the inflationary T cell pool. Inflationary memory CD8 T cells provided protection from a Vaccinia virus challenge and this protection directly correlated with the size of the inflationary memory T cell pool in peripheral tissues. These results highlight the remarkable protective potential of inflationary CD8 T cells that can be harnessed for CMV-based T cell vaccine approaches.

Indexed as

Adoptive TransferAnimalsCD8-Positive T-LymphocytesCytomegalovirus InfectionsFemaleImmunologic MemoryLectins, C-TypeMaleMiceMice, Inbred C57BLMuromegalovirusReceptors, ImmunologicKlrg1 protein, mouseLectins, C-TypeReceptors, Immunologic

Identifiers

PMID31083700
PMCPMC6532941
OpenAlexW2945931059

What OpenQuestion holds

Textmetadata
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.