Evidence map›Paper›PMID 37028427›Full record

ArticleImmunity2023

Long-term tolerance to skin commensals is established neonatally through a specialized dendritic cell subgroup.

Antonin Weckel, Miqdad O Dhariwala, Kevin Ly, Victoria M Tran, Oluwasunmisola T Ojewumi, Julianne B Riggs, Jeanmarie R Gonzalez, Laura R Dwyer, Joy N Okoro, John M Leech and 6 more

Open access · greenAbstract read
In one paragraph

Article in Immunity, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
8.7field-weighted citation impact, top 2% 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

36 citing papers in PubMed, 53 citations in OpenAlex.

  1. Article
  2. Article
  3. Conserved CD4Nature microbiology · 2026
    Article
  4. Review
  5. Article
  6. Beyond the skin barrier: commensalbioRxiv : the preprint server for biology · 2026
    Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. The human skin microbiome in health.Journal of the American Academy of Dermatology · 2025
    Review
  16. Article
  17. Article
  18. Review
  19. RORγt-expressing dendritic cells are functionally versatile and evolutionarily conserved antigen-presenting cells.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  20. Review
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

16 authors at 4 institutions in 2 countries.

Antonin WeckelUniversity of California, San Francisco, Department of Dermatology, San Francisco, CA 94143, USA.
Miqdad O DhariwalaUniversity of California, San Francisco, Department of Dermatology, San Francisco, CA 94143, USA.
Kevin LyUniversity of California, San Francisco, Department of Dermatology, San Francisco, CA 94143, USA; University of California, San Francisco, Biomedical Sciences Graduate Program, San Francisco, CA 94143, USA.
Victoria M TranUniversity of California, San Francisco, Department of Dermatology, San Francisco, CA 94143, USA; University of California, San Francisco, Biomedical Sciences Graduate Program, San Francisco, CA 94143, USA.
Oluwasunmisola T OjewumiUniversity of California, San Francisco, Department of Dermatology, San Francisco, CA 94143, USA.
Julianne B RiggsUniversity of California, San Francisco, Biomedical Sciences Graduate Program, San Francisco, CA 94143, USA.
Jeanmarie R GonzalezUniversity of California, San Francisco, Department of Dermatology, San Francisco, CA 94143, USA; University of California, San Francisco, Biomedical Sciences Graduate Program, San Francisco, CA 94143, USA.
Laura R DwyerUniversity of California, San Francisco, Department of Dermatology, San Francisco, CA 94143, USA; University of California, San Francisco, Biomedical Sciences Graduate Program, San Francisco, CA 94143, USA.
Joy N OkoroUniversity of California, San Francisco, Department of Dermatology, San Francisco, CA 94143, USA.
John M LeechUniversity of California, San Francisco, Department of Dermatology, San Francisco, CA 94143, USA.
Margot S BacinoUniversity of California, San Francisco, Oral and Craniofacial Sciences Graduate Program, San Francisco, CA 94143, USA.
Grace D ChoUniversity of California, San Francisco, Department of Dermatology, San Francisco, CA 94143, USA; University of California, Los Angeles, Department of Infectious Diseases, Los Angeles, CA 90095, USA.
Geil MeranaUniversity of California, San Francisco, Department of Dermatology, San Francisco, CA 94143, USA.
Niroshana AnandasabapathyDepartment of Dermatology, Meyer Cancer Center, Englander Institute for Precision Medicine, Weill Cornell Medical College, New York, NY, USA; Immunology and Microbial Pathogenesis Program, Weill Cornell Medical College, New York, NY, USA.
Yosuke KumamotoDepartment of Pathology, Immunology and Laboratory Medicine, Rutgers New Jersey Medical School, Newark, NJ 07103, USA; Center for Immunity and Inflammation, Rutgers New Jersey Medical School, Newark, NJ 07103, USA.
Tiffany C ScharschmidtUniversity of California, San Francisco, Department of Dermatology, San Francisco, CA 94143, USA. Electronic address: tiffany.scharschmidt@ucsf.edu.
University of California, San Francisco · USUniversity of San Francisco · USLander Institute · ILRutgers, The State University of New Jersey · US

Funding

Research BaseP30DK063720 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GERMAN, MICHAEL S · 2003 to 2019
$21.8M
MOLECULAR AND CELLULAR IMMUNOLOGYT32AI007334 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CYSTER, JASON G · 1988 to 2023
$11.0M
Interrogating unique DC adaptations to tissue to promote barrier immunity and toleranceR01AR080436 · NIAMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI Niroshana Anandasabapathy · 2022 to 2026
$3.5M
Functional Dissection of Regulatory Myeloid Cells in Microbe-Immune Crosstalk in SkinR01AR080034 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Tiffany Crawford Scharschmidt · 2022 to 2026
$2.9M
Decoding and harnessing microbial tuning of T cell responses in early lifeDP2AI144968 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SCHARSCHMIDT, TIFFANY CRAWFORD · 2018 to 2018
$2.4M
BD FACSAria Fusion Cell SorterS10OD021822 · OD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LEE, MICHAEL R. · 2016 to 2016
$573k
Elucidating microbial and host mechanisms supporting early life immune imprinting by skin monocytesK99AR079554 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI DHARIWALA, MIQDAD ONALI · 2021 to 2022
$178k
NIAID NIH HHS DP2 AI144968NIAID NIH HHS T32 AI007334NIAMS NIH HHS K99 AR079554NIAMS NIH HHS R01 AR080034NIAMS NIH HHS R01 AR080436NIDDK NIH HHS P30 DK063720NIH HHS S10 OD021822
6 · The paper itself

Abstract

Early-life establishment of tolerance to commensal bacteria at barrier surfaces carries enduring implications for immune health but remains poorly understood. Here, we showed that tolerance in skin was controlled by microbial interaction with a specialized subset of antigen-presenting cells. More particularly, CD301b

Indexed as

Dendritic CellsSkinAldehyde OxidoreductasesAnimalsHumansImmune ToleranceMiceT-Lymphocytes, RegulatoryAldehyde OxidoreductasesRALDH2 protein, mousecommensal bacteriacommensalsdendritic cellsearly-life immunityneonatal immunityregulatory T cellsretinoic acidskinStaphylococcus epidermidistolerance

Identifiers

PMID37028427
PMCPMC10330031
OpenAlexW4362664571

What OpenQuestion holds

Textmetadata
LicenceTDM
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.