Evidence map›Paper›PMID 26026054›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2015

Airway-Resident Memory CD8 T Cells Provide Antigen-Specific Protection against Respiratory Virus Challenge through Rapid IFN-γ Production.

Sean R McMaster, Jarad J Wilson, Hong Wang, Jacob E Kohlmeier

Abstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 179 papers.

0numbers the graph read from it
0cells of the map it votes in
179citing 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

179 citing papers in PubMed.

  1. Trial
  2. B cell-intrinsic CXCR3 drives efficient generation of ectopic pulmonary germinal center responses to influenza A virus infection.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. CD8MedComm · 2026
    Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Multivariate Host-Pathogen Interactions Driving Heterogeneous Viral Shedding and CD8medRxiv : the preprint server for health sciences · 2025
    Article
  16. Review
  17. bTInternational journal of molecular sciences · 2025
    Article
  18. Article
  19. Review
  20. Article

119 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

4 authors.

Sean R McMasterDepartment of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA 30322.
Jarad J WilsonDepartment of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA 30322.
Hong WangDepartment of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA 30322.
Jacob E KohlmeierDepartment of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA 30322 jkohlmeier@emory.edu.

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM008169 · NIGMS · EMORY UNIVERSITY · PI GROSS, ROBERT E · 1987 to 2021
$20.3M
TRAINING IN IMMUNOLOGY AND MOLECULAR PATHOGENESIST32AI007610 · NIAID · EMORY UNIVERSITY · PI EVAVOLD, BRIAN D · 2000 to 2014
$4.4M
Imprinting of Lung-Resident T Cell MemoryR01HL122559 · NHLBI · EMORY UNIVERSITY · PI KOHLMEIER, JACOB E · 2015 to 2019
$1.9M
The Role of CXCR6 in Lung Airway Memory T cell Recruitment and MaintenanceF30HL118954 · NHLBI · EMORY UNIVERSITY · PI MCMASTER, SEAN R · 2014 to 2016
$142k
NHLBI NIH HHS F30 HL118954NHLBI NIH HHS F30HL118954NHLBI NIH HHS HL122559NHLBI NIH HHS R01 HL122559NIAID NIH HHS HHSN266200700006CNIAID NIH HHS HHSN272201300006CNIAID NIH HHS T32 AI007610NIAID NIH HHS T32 AI007610-14NIGMS NIH HHS T32 GM008169PHS HHS HHSN266200700006C
6 · The paper itself

Abstract

CD8 airway resident memory T (TRM) cells are a distinctive TRM population with a high turnover rate and a unique phenotype influenced by their localization within the airways. Their role in mediating protective immunity to respiratory pathogens, although suggested by many studies, has not been directly proven. This study provides definitive evidence that airway CD8 TRM cells are sufficient to mediate protection against respiratory virus challenge. Despite being poorly cytolytic in vivo and failing to expand after encountering Ag, airway CD8 TRM cells rapidly express effector cytokines, with IFN-γ being produced most robustly. Notably, established airway CD8 TRM cells possess the ability to produce IFN-γ faster than systemic effector memory CD8 T cells. Furthermore, naive mice receiving intratracheal transfer of airway CD8 TRM cells lacking the ability to produce IFN-γ were less effective at controlling pathogen load upon heterologous challenge. This direct evidence of airway CD8 TRM cell-mediated protection demonstrates the importance of these cells as a first line of defense for optimal immunity against respiratory pathogens and suggests they should be considered in the development of future cell-mediated vaccines.

Indexed as

Adoptive TransferAnimalsAntigens, ViralCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell- and Tissue-Based TherapyHost-Pathogen InteractionsImmunologic MemoryInfluenza A Virus, H1N1 SubtypeInterferon-gammaLungMiceMice, Inbred C57BLMice, KnockoutOrthomyxoviridae InfectionsViral LoadAntigens, ViralInterferon-gamma

Identifiers

PMID26026054
PMCPMC4475417

What OpenQuestion holds

Textmetadata
LicenceTDM
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.