Evidence map›Paper›PMID 34504848›Full record

ArticleFrontiers in medicine2021

Single-Cell RNA Sequencing Reveals Cellular and Transcriptional Changes Associated With M1 Macrophage Polarization in Hidradenitis Suppurativa.

Paula Mariottoni, Simon W Jiang, Courtney A Prestwood, Vaibhav Jain, Jutamas Suwanpradid, Melodi Javid Whitley, Margaret Coates, David A Brown, Detlev Erdmann, David L Corcoran and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
6.8field-weighted citation impact, top 3% 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

39 citing papers in PubMed, 52 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. CD2 expressing innate lymphoid and T cells are critical effectors of immunopathogenesis in hidradenitis suppurativa.Proceedings of the National Academy of Sciences of the United States of America · 2024
    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

15 authors at 3 institutions in 1 country.

Paula MariottoniDepartment of Dermatology, School of Medicine, Duke University, Durham, NC, United States.
Simon W JiangDepartment of Dermatology, School of Medicine, Duke University, Durham, NC, United States.
Courtney A PrestwoodDepartment of Dermatology, University of Texas Southwestern Medical Center, Dallas, TX, United States.
Vaibhav JainDuke Molecular Physiology Institute, Duke University, Durham, NC, United States.
Jutamas SuwanpradidDepartment of Dermatology, School of Medicine, Duke University, Durham, NC, United States.
Melodi Javid WhitleyDepartment of Dermatology, School of Medicine, Duke University, Durham, NC, United States.
Margaret CoatesDepartment of Dermatology, School of Medicine, Duke University, Durham, NC, United States.
David A BrownDivision of Plastic, Maxillofacial, and Oral Surgery, Duke University Medical Center, Durham, NC, United States.
Detlev ErdmannDivision of Plastic, Maxillofacial, and Oral Surgery, Duke University Medical Center, Durham, NC, United States.
David L CorcoranDuke Center for Genomic and Computational Biology, Duke University, Durham, NC, United States.
Simon G GregoryDuke Molecular Physiology Institute, Duke University, Durham, NC, United States.
Tarannum JaleelDepartment of Dermatology, School of Medicine, Duke University, Durham, NC, United States.
Jennifer Y ZhangDepartment of Dermatology, School of Medicine, Duke University, Durham, NC, United States.
Tamia A Harris-TryonDepartment of Dermatology, University of Texas Southwestern Medical Center, Dallas, TX, United States.
Amanda S MacLeodDepartment of Dermatology, School of Medicine, Duke University, Durham, NC, United States.
Duke University · USDuke Medical Center · USThe University of Texas Southwestern Medical Center · 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
Duke-UNC Chapel Hill Immunotherapy Training GrantT32CA211056 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CHAO, NELSON J., SERODY, JONATHAN S. · 2017 to 2021
$2.2M
The Function of Small Proline Rich Proteins in Cutaneous Host DefenseK08AR076459 · NIAMS · UT SOUTHWESTERN MEDICAL CENTER · PI HARRIS-TRYON, TAMIA ALISHA · 2020 to 2024
$798k
NCI NIH HHS T32 CA211056NIAID NIH HHS R01 AI139207NIAMS NIH HHS K08 AR076459
6 · The paper itself

Abstract

Hidradenitis suppurativa (HS) is a chronic inflammatory skin disease characterized by recurrent abscesses, nodules, and sinus tracts in areas of high hair follicle and sweat gland density. These sinus tracts can present with purulent drainage and scar formation. Dysregulation of multiple immune pathways drives the complexity of HS pathogenesis and may account for the heterogeneity of treatment response in HS patients. Using transcriptomic approaches, including single-cell sequencing and protein analysis, we here characterize the innate inflammatory landscape of HS lesions. We identified a shared upregulation of genes involved in interferon (IFN) and antimicrobial defense signaling through transcriptomic overlap analysis of differentially expressed genes (DEGs) in datasets from HS skin, diabetic foot ulcers (DFUs), and the inflammatory stage of normal healing wounds. Overlap analysis between HS- and DFU-specific DEGs revealed an enrichment of gene signatures associated with monocyte/macrophage functions. Single-cell RNA sequencing further revealed monocytes/macrophages with polarization toward a pro-inflammatory M1-like phenotype and increased effector function, including antiviral immunity, phagocytosis, respiratory burst, and antibody-dependent cellular cytotoxicity. Specifically, we identified the STAT1/IFN-signaling axis and the associated IFN-stimulated genes as central players in monocyte/macrophage dysregulation. Our data indicate that monocytes/macrophages are a potential pivotal player in HS pathogenesis and their pathways may serve as therapeutic targets and biomarkers in HS treatment.

Indexed as

antiviral immune pathwayshidradenitis suppurativainterferonmacrophage-cellnon-healing woundssingle cell sequencing

Identifiers

PMID34504848
PMCPMC8421606
OpenAlexW3193720344

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.