Evidence map›Paper›PMID 26472076›Full record

ArticleAging cell2016

Reduced naïve CD8(+) T-cell priming efficacy in elderly adults.

Olivia Briceño, Anna Lissina, Kerstin Wanke, Georgia Afonso, Amrei von Braun, Kristanto Ragon, Tiphaine Miquel, Emma Gostick, Laura Papagno, Karin Stiasny and 5 more

Open access · goldAbstract read
In one paragraph

Article in Aging cell, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 101 papers.

0numbers the graph read from it
0cells of the map it votes in
101citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

101 citing papers in PubMed, 150 citations in OpenAlex.

  1. Trial
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  5. Renaissance of antiviral CD8Nature reviews. Immunology · 2026
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41 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

15 authors at 8 institutions in 4 countries.

Olivia BriceñoCentre d'Immunologie et des Maladies Infectieuses (CIMI-Paris), Sorbonne Universités, UPMC Univ Paris 06, DHU FAST, CR7, F-75013, Paris, France.
Anna LissinaCentre d'Immunologie et des Maladies Infectieuses (CIMI-Paris), Sorbonne Universités, UPMC Univ Paris 06, DHU FAST, CR7, F-75013, Paris, France.
Kerstin WankeDivision of Infectious Diseases, University Hospital of Zurich, Zurich, Switzerland.
Georgia AfonsoINSERM, U1016, Institut Cochin, Paris, France.
Amrei von BraunDivision of Infectious Diseases, University Hospital of Zurich, Zurich, Switzerland.
Kristanto RagonCentre d'Immunologie et des Maladies Infectieuses (CIMI-Paris), Sorbonne Universités, UPMC Univ Paris 06, DHU FAST, CR7, F-75013, Paris, France.
Tiphaine MiquelCentre d'Immunologie et des Maladies Infectieuses (CIMI-Paris), Sorbonne Universités, UPMC Univ Paris 06, DHU FAST, CR7, F-75013, Paris, France.
Emma GostickInstitute of Infection and Immunity, Cardiff University School of Medicine, Cardiff, Wales, UK.
Laura PapagnoCentre d'Immunologie et des Maladies Infectieuses (CIMI-Paris), Sorbonne Universités, UPMC Univ Paris 06, DHU FAST, CR7, F-75013, Paris, France.
Karin StiasnyDepartment of Virology, Medical University of Vienna, Vienna, Austria.
David A PriceInstitute of Infection and Immunity, Cardiff University School of Medicine, Cardiff, Wales, UK.
Roberto MalloneINSERM, U1016, Institut Cochin, Paris, France.
Delphine SauceCentre d'Immunologie et des Maladies Infectieuses (CIMI-Paris), Sorbonne Universités, UPMC Univ Paris 06, DHU FAST, CR7, F-75013, Paris, France.
Urs KarrerDivision of Infectious Diseases, University Hospital of Zurich, Zurich, Switzerland.
Victor AppayCentre d'Immunologie et des Maladies Infectieuses (CIMI-Paris), Sorbonne Universités, UPMC Univ Paris 06, DHU FAST, CR7, F-75013, Paris, France.
Sorbonne Université · FRUniversity Hospital of Zurich · CHCardiff University · GBCentre d'Immunologie et des Maladies Infectieuses · FRDélégation Paris 5 · FRHôpital Cochin · FRInserm · FRMedical University of Vienna · AT

Funding

Wellcome Trust 100326
6 · The paper itself

Abstract

Aging is associated with impaired vaccine efficacy and increased susceptibility to infectious and malignant diseases. CD8(+) T-cells are key players in the immune response against pathogens and tumors. In aged mice, the dwindling naïve CD8(+) T-cell compartment is thought to compromise the induction of de novo immune responses, but no experimental evidence is yet available in humans. Here, we used an original in vitro assay based on an accelerated dendritic cell coculture system in unfractioned peripheral blood mononuclear cells to examine CD8(+) T-cell priming efficacy in human volunteers. Using this approach, we report that old individuals consistently mount quantitatively and qualitatively impaired de novo CD8(+) T-cell responses specific for a model antigen. Reduced CD8(+) T-cell priming capacity in vitro was further associated with poor primary immune responsiveness in vivo. This immune deficit likely arises as a consequence of intrinsic cellular defects and a reduction in the size of the naïve CD8(+) T-cell pool. Collectively, these findings provide new insights into the cellular immune insufficiencies that accompany human aging.

Indexed as

AdultAgedAged, 80 and overAgingCD8-Positive T-LymphocytesDendritic CellsFemaleFlow CytometryHumansLeukocytes, MononuclearLymphocyte ActivationMaleMiddle AgedYoung Adultagingnaïve CD8+ T-cellspriming

Identifiers

PMID26472076
PMCPMC4717282
OpenAlexW1930328534

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.