Evidence map›Paper›PMID 27217536›Full record

ArticleThe Journal of experimental medicine2016

Local antigen in nonlymphoid tissue promotes resident memory CD8+ T cell formation during viral infection.

Tahsin N Khan, Jana L Mooster, Augustus M Kilgore, Jossef F Osborn, Jeffrey C Nolz

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 153 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
153citing papers in PubMed, 1 pooled it
13.5field-weighted citation impact, top 1% 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

153 citing papers in PubMed, 1 synthesis or guideline pooled it, 205 citations in OpenAlex.

  1. Tissue-Resident Memory T Cells in Skin Diseases: A Systematic Review.International journal of molecular sciences · 2021
    Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. PD-1 is requisite for skin TNature immunology · 2025
    Article
  12. Cutaneous T cell immunity.Nature immunology · 2025
    Review
  13. Article
  14. CXCR6 promotes dermal CD8bioRxiv : the preprint server for biology · 2025
    Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Review
  20. Innovative Hydrogel Design: Tailoring Immunomodulation for Optimal Chronic Wound Recovery.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review

93 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

5 authors at 1 institution in 1 country.

Tahsin N KhanDepartment of Molecular Microbiology and Immunology, Oregon Health and Science University, Portland, OR 97239.
Jana L MoosterDepartment of Molecular Microbiology and Immunology, Oregon Health and Science University, Portland, OR 97239.
Augustus M KilgoreDepartment of Molecular Microbiology and Immunology, Oregon Health and Science University, Portland, OR 97239.
Jossef F OsbornDepartment of Molecular Microbiology and Immunology, Oregon Health and Science University, Portland, OR 97239.
Jeffrey C NolzDepartment of Molecular Microbiology and Immunology, Oregon Health and Science University, Portland, OR 97239 Department of Cell, Developmental, and Cancer Biology, Oregon Health and Science University, Portland, OR 97239 Department of Radiation Medicine, Oregon Health and Science University, Portland, OR 97239 nolz@ohsu.edu.
Oregon Health & Science University · US

Funding

Understanding the origins of rapid recurrence of pancreatic cancer after resectionP30CA069533 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Luiz Eduardo Bertassoni · 1997 to 2026
$60.5M
Regulation of Memory CD8 T cell Trafficking to Inflamed TissuesK22AI102981 · NIAID · OREGON HEALTH & SCIENCE UNIVERSITY · PI NOLZ, JEFFREY C. · 2014 to 2015
$270k
NCI NIH HHS P30 CA069533NIAID NIH HHS K22 AI102981
6 · The paper itself

Abstract

Tissue-resident memory (Trm) CD8(+) T cells are functionally distinct from their circulating counterparts and are potent mediators of host protection against reinfection. Whether local recognition of antigen in nonlymphoid tissues during infection can impact the formation of Trm populations remains unresolved. Using skin infections with vaccinia virus (VacV)-expressing model antigens, we found that local antigen recognition had a profound impact on Trm formation. Activated CD8(+) T cells trafficked to VacV-infected skin in an inflammation-dependent, but antigen-independent, manner. However, after viral clearance, there was a subsequent ∼50-fold increase in Trm formation when antigen was present in the tissue microenvironment. Secondary antigen stimulation in nonlymphoid tissue caused CD8(+) T cells to rapidly express CD69 and be retained at the site of infection. Finally, Trm CD8(+) T cells that formed during VacV infection in an antigen-dependent manner became potent stimulators of localized antigen-specific inflammatory responses in the skin. Thus, our studies indicate that the presence of antigen in the nonlymphoid tissue microenvironment plays a critical role in the formation of functional Trm CD8(+) T cell populations, a finding with relevance for both vaccine design and prevention of inflammatory disorders.

Indexed as

Immunologic MemoryModels, ImmunologicalAnimalsAntigens, CDAntigens, Differentiation, T-LymphocyteAntigens, ViralCD69 AntigensCD8-Positive T-LymphocytesLectins, C-TypeMiceMice, TransgenicSkinVacciniaVaccinia virusAntigens, CDAntigens, Differentiation, T-LymphocyteAntigens, ViralCD69 AntigensLectins, C-Type

Identifiers

PMID27217536
PMCPMC4886364
OpenAlexW2405078719

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.