Evidence map›Paper›PMID 25609844›Full record

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

Dermal-resident versus recruited γδ T cell response to cutaneous vaccinia virus infection.

Amanda S Woodward Davis, Tessa Bergsbaken, Martha A Delaney, Michael J Bevan

Open access · bronzeAbstract 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 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Murine CXCR3Frontiers in immunology · 2021
    Article
  7. Review
  8. Immunological memories of the bone marrow.Immunological reviews · 2018
    Review
  9. Article
  10. IL-1β and IL-23 Promote Extrathymic Commitment of CD27Journal of immunology (Baltimore, Md. : 1950) · 2017
    Article
  11. Article
  12. Article
  13. Article
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 at 1 institution in 1 country.

Amanda S Woodward DavisDepartment of Immunology, University of Washington, Seattle, WA 98109;
Tessa BergsbakenDepartment of Immunology, University of Washington, Seattle, WA 98109; Howard Hughes Medical Institute, University of Washington, Seattle, WA 98109; and.
Martha A DelaneyDepartment of Comparative Medicine, University of Washington, Seattle, WA 98109.
Michael J BevanDepartment of Immunology, University of Washington, Seattle, WA 98109; Howard Hughes Medical Institute, University of Washington, Seattle, WA 98109; and mbevan@uw.edu.
University of Washington · US

Funding

Howard Hughes Medical Institute
6 · The paper itself

Abstract

The study of T cell immunity at barrier surfaces has largely focused on T cells bearing the αβ TCR. However, T cells that express the γδ TCR are disproportionately represented in peripheral tissues of mice and humans, suggesting they too may play an important role responding to external stimuli. In this article, we report that, in a murine model of cutaneous infection with vaccinia virus, dermal γδ T cell numbers increased 10-fold in the infected ear and resulted in a novel γδ T cell population not found in naive skin. Circulating γδ T cells were specifically recruited to the site of inflammation and differentially contributed to dermal populations based on their CD27 expression. Recruited γδ T cells, the majority of which were CD27(+), were granzyme B(+) and made up about half of the dermal population at the peak of the response. In contrast, recruited and resident γδ T cell populations that made IL-17 were CD27(-). Using a double-chimera model that can discriminate between the resident dermal and recruited γδ T cell populations, we demonstrated their divergent functions and contributions to early stages of tissue inflammation. Specifically, the loss of the perinatal thymus-derived resident dermal population resulted in decreased cellularity and collateral damage in the tissue during viral infection. These findings have important implications for our understanding of immune coordination at barrier surfaces and the contribution of innate-like lymphocytes on the front lines of immune defense.

Indexed as

AnimalsCell MovementChimeraDermisEarGene Expression RegulationGranzymesImmunity, InnateInterleukin-17Lymph NodesMiceMice, Inbred C57BLMice, KnockoutPoxviridae InfectionsReceptors, Antigen, T-Cell, gamma-deltaSignal TransductionGranzymesGzmb protein, mouseInterleukin-17Receptors, Antigen, T-Cell, gamma-deltaTumor Necrosis Factor Receptor Superfamily, Member 7

Identifiers

PMID25609844
PMCPMC4340759
OpenAlexW2123276466

What OpenQuestion holds

Textmetadata
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.