Evidence map›Paper›PMID 39225100›Full record

ArticleThe Journal of clinical investigation2024

Recruitment of CXCR4+ type 1 innate lymphoid cells distinguishes sarcoidosis from other skin granulomatous diseases.

Satish Sati, Jianhe Huang, Anna E Kersh, Parker Jones, Olivia Ahart, Christina Murphy, Stephen M Prouty, Matthew L Hedberg, Vaibhav Jain, Simon G Gregory and 4 more

Abstract read
In one paragraph

Article in The Journal of clinical investigation, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. SiteCELL enablesiScience · 2026
    Article
  3. New Therapies for Sarcoidosis: Molecular and Pathophysiological Basis.International journal of molecular sciences · 2026
    Review
  4. The inflammatory fingerprint reveals immune cell populations associated with disease activity in cardiac sarcoidosis.Clinical research in cardiology : official journal of the German Cardiac Society · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Detection by Single-Cell RNA Sequencing of Virally Mediated Skin Diseases.JID innovations : skin science from molecules to population health · 2025
    Article
  10. Review
  11. 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

14 authors.

Satish SatiDepartment of Dermatology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.
Jianhe HuangDepartment of Dermatology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.
Anna E KershDepartment of Dermatology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.
Parker JonesDepartment of Dermatology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.
Olivia AhartDepartment of Dermatology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.
Christina MurphyDepartment of Dermatology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.
Stephen M ProutyDepartment of Dermatology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.
Matthew L HedbergDepartment of Dermatology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.
Vaibhav JainDuke Molecular Physiology Institute, Durham, North Carolina, USA.
Simon G GregoryDuke Molecular Physiology Institute, Durham, North Carolina, USA.
Denis H LeungSingapore Management University, Singapore.
John T SeykoraDepartment of Dermatology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.
Misha RosenbachDepartment of Dermatology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.
Thomas H LeungDepartment of Dermatology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.

Funding

Study Design and Data AnalysisP30AR069589 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI Elizabeth Anne Grice · 2016 to 2026
$8.6M
Neuroimmune Control of Scarless Skin RegenerationR01AR079483 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI LEUNG, THOMAS H. · 2021 to 2025
$1.9M
Immune and Genetic Controls of Tissue Regeneration in Mice and HumansI01RX002701 · VA · PHILADELPHIA VA MEDICAL CENTER · PI Thomas H. Leung · 2018 to 2026
–
NIAMS NIH HHS P30 AR069589NIAMS NIH HHS R01 AR079483RRD VA I01 RX002701
6 · The paper itself

Abstract

Sarcoidosis is a multiorgan granulomatous disease that lacks diagnostic biomarkers and targeted treatments. Using blood and skin from patients with sarcoid and non-sarcoid skin granulomas, we discovered that skin granulomas from different diseases exhibit unique immune cell recruitment and molecular signatures. Sarcoid skin granulomas were specifically enriched for type 1 innate lymphoid cells (ILC1s) and B cells and exhibited molecular programs associated with formation of mature tertiary lymphoid structures (TLSs), including increased CXCL12/CXCR4 signaling. Lung sarcoidosis granulomas also displayed similar immune cell recruitment. Thus, granuloma formation was not a generic molecular response. In addition to tissue-specific effects, patients with sarcoidosis exhibited an 8-fold increase in circulating ILC1s, which correlated with treatment status. Multiple immune cell types induced CXCL12/CXCR4 signaling in sarcoidosis, including Th1 T cells, macrophages, and ILCs. Mechanistically, CXCR4 inhibition reduced sarcoidosis-activated immune cell migration, and targeting CXCR4 or total ILCs attenuated granuloma formation in a noninfectious mouse model. Taken together, our results show that ILC1s are a tissue and circulating biomarker that distinguishes sarcoidosis from other skin granulomatous diseases. Repurposing existing CXCR4 inhibitors may offer a new targeted treatment for this devastating disease.

Indexed as

GranulomaImmunity, InnateReceptors, CXCR4SarcoidosisAnimalsChemokine CXCL12FemaleHumansLymphocytesMaleMiceSignal TransductionSkinSkin DiseasesChemokine CXCL12CXCL12 protein, humanCXCR4 protein, humanCXCR4 protein, mouseReceptors, CXCR4Cellular immune responseDermatologyImmunologyInnate immunity

Identifiers

PMID39225100
PMCPMC11364400

What Socratic 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 Socratic graph.