Evidence map›Paper›PMID 31801072›Full record

ArticleCell reports2019

Langerhans Cells Orchestrate the Protective Antiviral Innate Immune Response in the Lymph Node.

Eric Wong, Brian Montoya, Colby Stotesbury, Maria Ferez, Ren-Huan Xu, Luis J Sigal

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

17 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Review
  3. Langerhans cells: Central players in the pathophysiology of atopic dermatitis.Journal of the European Academy of Dermatology and Venereology : JEADV · 2025
    Review
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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

6 authors at 2 institutions in 1 country.

Eric WongDepartment of Microbiology and Immunology, Thomas Jefferson University, BLSB 709 233 South 10(th) Street, Philadelphia, PA 19107, USA.
Brian MontoyaDepartment of Microbiology and Immunology, Thomas Jefferson University, BLSB 709 233 South 10(th) Street, Philadelphia, PA 19107, USA.
Colby StotesburyDepartment of Microbiology and Immunology, Thomas Jefferson University, BLSB 709 233 South 10(th) Street, Philadelphia, PA 19107, USA.
Maria FerezDepartment of Microbiology and Immunology, Thomas Jefferson University, BLSB 709 233 South 10(th) Street, Philadelphia, PA 19107, USA.
Ren-Huan XuImmune Cell Development and Host Defense Program, Research Institute of Fox Chase Cancer Center, 333 Cottman Avenue, Philadelphia, PA 19111, USA.
Luis J SigalDepartment of Microbiology and Immunology, Thomas Jefferson University, BLSB 709 233 South 10(th) Street, Philadelphia, PA 19107, USA. Electronic address: luis.sigal@jefferson.edu.
Thomas Jefferson University · USFox Chase Cancer Center · US

Funding

X-Ray Crystallography and Macromolecular CharacterizationP30CA056036 · NCI · THOMAS JEFFERSON UNIVERSITY · PI Andrew Chapman · 1995 to 2026
$94.8M
Orthropoxvirus Pathogenesis and VaccinesR01AI065544 · NIAID · THOMAS JEFFERSON UNIVERSITY · PI SIGAL, LUIS J · 2006 to 2016
$5.7M
MHC Class I Antigen Presentation in Viral InfectionsR01AI048849 · NIAID · RESEARCH INST OF FOX CHASE CAN CTR · PI SIGAL, LUIS J · 2001 to 2011
$3.8M
Inflammatory monocytes in the draining lymph node of ECTV infected miceR01AI110457 · NIAID · THOMAS JEFFERSON UNIVERSITY · PI SIGAL, LUIS J · 2015 to 2019
$2.3M
Natural Killer Cell Deficiencies in Aging MiceR01AG048602 · NIA · THOMAS JEFFERSON UNIVERSITY · PI SIGAL, LUIS J · 2014 to 2018
$1.8M
Training grant on Vaccines and Immunotherapies for Infectious Diseases and CancerT32AI134646 · NIAID · THOMAS JEFFERSON UNIVERSITY · PI SCHNELL, MATTHIAS JOHANNES, SIGAL, LUIS J · 2018 to 2022
$1.1M
The role of skin-derived, migratory dendritic cells in ectromelia-infected miceF32AI129352 · NIAID · THOMAS JEFFERSON UNIVERSITY · PI WONG, ERIC · 2017 to 2019
$144k
NCI NIH HHS P30 CA056036NIAID NIH HHS F32 AI129352NIAID NIH HHS R01 AI048849NIAID NIH HHS R01 AI065544NIAID NIH HHS R01 AI110457NIAID NIH HHS T32 AI134646NIA NIH HHS R01 AG048602
6 · The paper itself

Abstract

During disseminating viral infections, a swift innate immune response (IIR) in the draining lymph node (dLN) that restricts systemic viral spread is critical for optimal resistance to disease. However, it is unclear how this IIR is orchestrated. We show that after footpad infection of mice with ectromelia virus, dendritic cells (DCs) highly expressing major histocompatibility complex class II (MHC class II

Indexed as

AnimalsAntiviral AgentsCell LineCell MovementCytokinesDendritic CellsFemaleHistocompatibility Antigens Class IIImmunity, InnateLangerhans CellsLymph NodesMaleMiceMice, Inbred C57BLSkinUp-RegulationAntiviral AgentsCytokinesHistocompatibility Antigens Class IIdendritic cellsectromelia virusinflammatory monocytesLangerhans cellslymph nodenatural killer cellsskinvirus infection

Identifiers

PMID31801072
PMCPMC6927544
OpenAlexW2993457448

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.