Evidence map›Paper›PMID 26687547›Full record

ArticleNature communications2015

RSV-specific airway resident memory CD8+ T cells and differential disease severity after experimental human infection.

Agnieszka Jozwik, Maximillian S Habibi, Allan Paras, Jie Zhu, Aleks Guvenel, Jaideep Dhariwal, Mark Almond, Ernie H C Wong, Annemarie Sykes, Matthew Maybeno and 10 more

Erratum issued Registry-linked trialAbstract read
In one paragraph

Article in Nature communications, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT02755948 (Cell Mediated Immunity Against RSV and Influenza in a Human Experimental Challenge), which is not on this map. Cited by 212 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
212citing papers in PubMed, 1 pooled it
–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.

NCT02755948 nacompletednot on this map

Cell Mediated Immunity Against RSV and Influenza in a Human Experimental Challenge

TypeinterventionalSponsorImperial College LondonRan2012 to 2020Enrolled75ConditionsRespiratory Syncytial Virus Infections, Influenza, HumanArmsRSV A Memphis 37, Influenza A/California/04/2009-likw (H1N1), Influenza A/Belgium/4217/2015 (H3N2)
3 · Its place in the literature

Who cites it

212 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Immune persistence and safety of the AS01Human vaccines & immunotherapeutics · 2025
    Trial
  3. Trial
  4. Trial
  5. Trial
  6. Innate-like Gene Expression of Lung-Resident Memory CD8American journal of respiratory and critical care medicine · 2021
    Trial
  7. Trial
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. The ageing immune system and its battle with viruses.The Journal of general virology · 2026
    Review
  15. Review
  16. RelA Signaling inInternational journal of molecular sciences · 2026
    Article
  17. Article
  18. Observational
  19. Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors.

Agnieszka JozwikNational Heart and Lung Institute, Imperial College London, London W2 1PG, UK.
Maximillian S HabibiNational Heart and Lung Institute, Imperial College London, London W2 1PG, UK.
Allan ParasNational Heart and Lung Institute, Imperial College London, London W2 1PG, UK.
Jie ZhuNational Heart and Lung Institute, Imperial College London, London W2 1PG, UK.
Aleks GuvenelNational Heart and Lung Institute, Imperial College London, London W2 1PG, UK.
Jaideep DhariwalNational Heart and Lung Institute, Imperial College London, London W2 1PG, UK.
Mark AlmondNational Heart and Lung Institute, Imperial College London, London W2 1PG, UK.
Ernie H C WongNational Heart and Lung Institute, Imperial College London, London W2 1PG, UK.
Annemarie SykesNational Heart and Lung Institute, Imperial College London, London W2 1PG, UK.
Matthew MaybenoCentre for Infectious Disease, Division of Vaccine Discovery, La Jolla Institute of Allergy and Immunology, 9420 Athena Circle, La Jolla, California 92037, USA.
Jerico Del RosarioNational Heart and Lung Institute, Imperial College London, London W2 1PG, UK.
Maria-Belen Trujillo-TorralboNational Heart and Lung Institute, Imperial College London, London W2 1PG, UK.
Patrick MalliaNational Heart and Lung Institute, Imperial College London, London W2 1PG, UK.
John SidneyCentre for Infectious Disease, Division of Vaccine Discovery, La Jolla Institute of Allergy and Immunology, 9420 Athena Circle, La Jolla, California 92037, USA.
Bjoern PetersCentre for Infectious Disease, Division of Vaccine Discovery, La Jolla Institute of Allergy and Immunology, 9420 Athena Circle, La Jolla, California 92037, USA.ORCID http://orcid.org/0000-0002-8457-6693
Onn Min KonNational Heart and Lung Institute, Imperial College London, London W2 1PG, UK.
Alessandro SetteCentre for Infectious Disease, Division of Vaccine Discovery, La Jolla Institute of Allergy and Immunology, 9420 Athena Circle, La Jolla, California 92037, USA.
Sebastian L JohnstonNational Heart and Lung Institute, Imperial College London, London W2 1PG, UK.
Peter J OpenshawNational Heart and Lung Institute, Imperial College London, London W2 1PG, UK.
Christopher ChiuNational Heart and Lung Institute, Imperial College London, London W2 1PG, UK.ORCID http://orcid.org/0000-0003-0914-920X

Funding

Medical Research Council G0700552Medical Research Council G0902266Medical Research Council G1000758Wellcome TrustWellcome Trust 087805/Z/08/Z
6 · The paper itself

Abstract

In animal models, resident memory CD8+ T (Trm) cells assist in respiratory virus elimination but their importance in man has not been determined. Here, using experimental human respiratory syncytial virus (RSV) infection, we investigate systemic and local virus-specific CD8+ T-cell responses in adult volunteers. Having defined the immunodominance hierarchy, we analyse phenotype and function longitudinally in blood and by serial bronchoscopy. Despite rapid clinical recovery, we note surprisingly extensive lower airway inflammation with persistent viral antigen and cellular infiltrates. Pulmonary virus-specific CD8+ T cells display a CD69+CD103+ Trm phenotype and accumulate to strikingly high frequencies into convalescence without continued proliferation. While these have a more highly differentiated phenotype, they express fewer cytotoxicity markers than in blood. Nevertheless, their abundance before infection correlates with reduced symptoms and viral load, implying that CD8+ Trm cells in the human lung can confer protection against severe respiratory viral disease when humoral immunity is overcome.

Indexed as

Immunologic MemoryAdolescentAdultAnimalsCD8-Positive T-LymphocytesCell DifferentiationFemaleHumansLungMaleMiceMiddle AgedRespiratory Syncytial VirusesRespiratory Syncytial Virus InfectionsYoung Adult

Identifiers

PMID26687547
PMCPMC4703893

What OpenQuestion holds

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Registered trials

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.