Evidence map›Paper›PMID 27191829›Full record

ArticleVirulence2016

Batf3-dependent CD103(+) dendritic cell accumulation is dispensable for mucosal and systemic antifungal host defense.

Timothy J Break, Kevin W Hoffman, Muthulekha Swamydas, Chyi-Chia Richard Lee, Jean K Lim, Michail S Lionakis

Open access · goldAbstract read
In one paragraph

Article in Virulence, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

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  10. Radiation Followed by OX40 Stimulation Drives Local and Abscopal Antitumor Effects in an Anti-PD1-Resistant Lung Tumor Model.Clinical cancer research : an official journal of the American Association for Cancer Research · 2018
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 1 country.

Timothy J Breaka Fungal Pathogenesis Unit, Laboratory of Clinical Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health , Bethesda , MD , USA.
Kevin W Hoffmanb Department of Microbiology , Icahn School of Medicine at Mount Sinai , New York , NY , USA.
Muthulekha Swamydasa Fungal Pathogenesis Unit, Laboratory of Clinical Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health , Bethesda , MD , USA.
Chyi-Chia Richard Leec Laboratory of Pathology, Center for Cancer Research, National Cancer Institute, National Institutes of Health , Bethesda , MD , USA.
Jean K Limb Department of Microbiology , Icahn School of Medicine at Mount Sinai , New York , NY , USA.
Michail S Lionakisa Fungal Pathogenesis Unit, Laboratory of Clinical Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health , Bethesda , MD , USA.
Icahn School of Medicine at Mount Sinai · USNational Institutes of Health · USCenter for Cancer Research · USNational Institute of Allergy and Infectious Diseases · US

Funding

Immunopathogenesis of Fungal InfectionsZIAAI001175 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI LIONAKIS, MICHAIL · 2012 to 2025
$23.9M
TRAINING PROGRAM: MECHANISMS OF VIRUS-HOST INTERACTIONST32AI007647 · NIAID · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI Domenico Tortorella · 2000 to 2026
$11.5M
Chemokine regulation of myeloid cell populations during West Nile virus infectionR01AI108715 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI LIM, JEAN KYOU · 2014 to 2017
$1.4M
NIAID NIH HHS R01 AI108715NIAID NIH HHS T32 AI007647
6 · The paper itself

Abstract

Dendritic cells (DCs) are critical for defense against a variety of pathogens and the formation of adaptive immune responses. The transcription factor Batf3 is critical for the development of CD103(+)CD11b(-) DCs, which promote IL-12-dependent protective immunity during viral and parasitic infections, dampen Th2 immunity during helminthic infection, and exert detrimental effects during bacterial infection. Whether CD103(+) DCs modulate immunity during systemic or mucosal fungal disease remains unknown. Herein, we report that Batf3 is critical for accumulation of CD103(+) DCs in the kidney and tongue at steady state, for their expansion during systemic and oropharyngeal candidiasis, and for tissue-specific production of IL-12 in kidney but not tongue during systemic and oropharyngeal candidiasis, respectively. Importantly, deficiency of CD103(+) DCs does not impair survival or fungal clearance during systemic or oropharyngeal candidiasis, indicating that Batf3-dependent CD103(+) DC accumulation mediates pathogen- and tissue-specific immune effects.

Indexed as

AnimalsAntigens, CDBasic-Leucine Zipper Transcription FactorsCandidiasis, InvasiveCandidiasis, OralCell ProliferationDendritic CellsImmunity, InnateIntegrin alpha ChainsInterleukin-12KidneyMiceMice, Inbred C57BLRepressor ProteinsTonguealpha E integrinsAntigens, CDBasic-Leucine Zipper Transcription FactorsIntegrin alpha ChainsInterleukin-12Repressor ProteinsSNFT protein, mouseBatf3CD103dendritic cellsfungal infectionIL-12innate immunityoropharyngeal candidiasissystemic candidiasis

Identifiers

PMID27191829
PMCPMC5029292
OpenAlexW2406721578

What OpenQuestion holds

Textmetadata
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.