Evidence map›Paper›PMID 34659203›Full record

ArticleFrontiers in immunology2021

IL-27 Derived From Macrophages Facilitates IL-15 Production and T Cell Maintenance Following Allergic Hypersensitivity Responses.

Jutamas Suwanpradid, Min Jin Lee, Peter Hoang, Jeffery Kwock, Lauren P Floyd, Jeffrey S Smith, Zhinan Yin, Amber R Atwater, Sudarshan Rajagopal, Ross M Kedl and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

14 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. IL-27-induced PD-L1Experimental & molecular medicine · 2024
    Article
  8. Article
  9. Role of Innate Immunity in Allergic Contact Dermatitis: An Update.International journal of molecular sciences · 2023
    Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. 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

13 authors at 3 institutions in 2 countries.

Jutamas SuwanpradidDepartment of Dermatology, Duke University, Durham, NC, United States.
Min Jin LeeDepartment of Dermatology, Duke University, Durham, NC, United States.
Peter HoangDepartment of Dermatology, Duke University, Durham, NC, United States.
Jeffery KwockDepartment of Dermatology, Duke University, Durham, NC, United States.
Lauren P FloydDepartment of Dermatology, Duke University, Durham, NC, United States.
Jeffrey S SmithDepartment of Biochemistry, Duke University, Durham, NC, United States.
Zhinan YinZhuhai Institute of Translational Medicine Zhuhai People's Hospital Affiliated with Jinan University, Jinan University, Zhuhai, China.
Amber R AtwaterDepartment of Dermatology, Duke University, Durham, NC, United States.
Sudarshan RajagopalDepartment of Biochemistry, Duke University, Durham, NC, United States.
Ross M KedlDepartment of Immunology and Microbiology, University of Colorado Anschutz School of Medicine, Aurora, CO, United States.
David L CorcoranCenter for Genomic and Computational Biology, Duke University, Durham, NC, United States.
Jennifer Y ZhangDepartment of Dermatology, Duke University, Durham, NC, United States.
Amanda S MacLeodDepartment of Dermatology, Duke University, Durham, NC, United States.
Duke University · USJinan University · CNUniversity of Colorado Anschutz Medical Campus · US

Funding

Dynamic Control of Innate Antiviral Immunity in Skin Homeostasis and InflammationR01AI139207 · NIAID · DUKE UNIVERSITY · PI ZHANG, JENNIFER YUNYAN · 2018 to 2022
$3.2M
NIAID NIH HHS R01 AI139207
6 · The paper itself

Abstract

Crosstalk between T cells, dendritic cells, and macrophages in temporal leukocyte clusters within barrier tissues provides a new concept for T cell activation in the skin. Activated T cells from these leukocyte clusters play critical roles in the efferent phase of allergic contact hypersensitivity (CHS). However, the cytokines driving maintenance and survival of pathogenic T cells during and following CHS remain mostly unknown. Upon epicutaneous allergen challenge, we here report that macrophages produce IL-27 which then induces IL-15 production from epidermal keratinocytes and dermal myeloid cells within leukocyte clusters. In agreement with the known role of IL-15 as a T cell survival factor and growth cytokine, this signaling axis enhances BCL2 and survival of skin T cells. Genetic depletion or pharmacological blockade of IL-27 in CHS mice leads to abrogated epidermal IL-15 production resulting in a decrease in BCL2 expression in T cells and a decline in dermal CD8

Indexed as

AllergensAnimalsBiomarkersDisease Models, AnimalDisease SusceptibilityHumansHypersensitivityInterleukin-15Interleukin-27KeratinocytesMacrophagesMiceMyeloid CellsSkinTHP-1 CellsT-LymphocytesAllergensBiomarkersInterleukin-15Interleukin-27BCL2CD172acontact hypersensitivitydermal leukocyte clusterhuman allergic contact dermatitisIL-15IL-27STAT1

Identifiers

PMID34659203
PMCPMC8515907
OpenAlexW3202087660

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.