Evidence map›Paper›PMID 37414907›Full record

ArticleNature immunology2023

Transitional dendritic cells are distinct from conventional DC2 precursors and mediate proinflammatory antiviral responses.

Fernando Bandeira Sulczewski, Raul A Maqueda-Alfaro, Marcela Alcántara-Hernández, Oriana A Perez, Sanjana Saravanan, Tae Jin Yun, David Seong, Rebeca Arroyo Hornero, Hayley M Raquer-McKay, Eduardo Esteva and 8 more

Open access · greenAbstract read
In one paragraph

Article in Nature immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
12.8field-weighted citation impact, top 1% 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

60 citing papers in PubMed, 78 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 3 institutions in 1 country.

Fernando Bandeira Sulczewski *Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.
Raul A Maqueda-Alfaro *Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.ORCID http://orcid.org/0000-0003-3538-1176
Marcela Alcántara-Hernández *Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.
Oriana A PerezDepartment of Pathology, New York University Grossman School of Medicine, New York, NY, USA.
Sanjana SaravananDepartment of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.ORCID http://orcid.org/0000-0002-5974-7710
Tae Jin YunDepartment of Pathology, New York University Grossman School of Medicine, New York, NY, USA.
David SeongDepartment of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.
Rebeca Arroyo HorneroDepartment of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.ORCID http://orcid.org/0000-0001-7026-7358
Hayley M Raquer-McKayDepartment of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.ORCID http://orcid.org/0000-0002-7404-8221
Eduardo EstevaDepartment of Pathology, New York University Grossman School of Medicine, New York, NY, USA.
Zachary R LanzarDepartment of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.
Rebecca A LeylekDepartment of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.
Nicholas M AdamsDepartment of Pathology, New York University Grossman School of Medicine, New York, NY, USA.ORCID http://orcid.org/0000-0001-5751-0480
Annesa DasDepartment of Pathology, New York University Grossman School of Medicine, New York, NY, USA.
Adeeb H RahmanMarc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Andres Gottfried-BlackmoreDepartment of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.
Boris ReizisDepartment of Pathology, New York University Grossman School of Medicine, New York, NY, USA. Boris.Reizis@nyulangone.org.ORCID http://orcid.org/0000-0003-1140-7853
Juliana IdoyagaDepartment of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA. jidoyaga@stanford.edu.ORCID http://orcid.org/0000-0002-4430-8862
Stanford University · USNew York University · USIcahn School of Medicine at Mount Sinai · US

Funding

Viral Assays CoreU19AI128949 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Donna L. Farber, Peter Alan Sims · 2017 to 2026
$26.4M
Institutional Career Development Core (KL2)KL2TR003143 · NCATS · STANFORD UNIVERSITY · PI ASCH, STEVEN M. · 2019 to 2023
$8.7M
Molecular Control of Plasmacytoid Dendritic Cell Development and FunctionR37AI072571 · NIAID · UNIVERSITY OF CHICAGO · PI Boris Reizis · 2018 to 2026
$5.3M
Molecular Control of Plasmacytoid Dendritic Cell Development and FunctionR01AI072571 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI REIZIS, BORIS · 2008 to 2017
$4.1M
Transitional dendritic cells: identifying the origin and role of a novel innate immune population during viral infectionR01AI158808 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Juliana Idoyaga · 2021 to 2026
$3.5M
CyTOFS10OD016318 · OD · STANFORD UNIVERSITY · PI NOLAN, GARRY P · 2013 to 2013
$600k
Novel genetic tools for the analysis of plasmacytoid dendritic cell function in vivoR21AI147501 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI REIZIS, BORIS · 2019 to 2020
$466k
Novel transcription factors modulating the development and function of pDCs and pDC-related cellsR21AI163775 · NIAID · STANFORD UNIVERSITY · PI IDOYAGA, JULIANA · 2021 to 2022
$437k
Dynamic Spatiotemporal Analysis of Immune Cells in the Tumor MicroenvironmentF32CA232666 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI PEREZ, ORIANA · 2018 to 2020
$150k
NCATS NIH HHS KL2 TR003143NCATS NIH HHS KL2TR003143NCI NIH HHS CA232666NCI NIH HHS F32 CA232666NIAID NIH HHS AI072571NIAID NIH HHS AI128949NIAID NIH HHS AI147501NIAID NIH HHS AI158808NIAID NIH HHS AI163775NIAID NIH HHS R01 AI072571NIAID NIH HHS R01 AI158808NIAID NIH HHS R21 AI147501NIAID NIH HHS R21 AI163775NIAID NIH HHS R37 AI072571NIAID NIH HHS U19 AI128949NIH HHS S10 OD016318
6 · The paper itself

Abstract

High-dimensional approaches have revealed heterogeneity amongst dendritic cells (DCs), including a population of transitional DCs (tDCs) in mice and humans. However, the origin and relationship of tDCs to other DC subsets has been unclear. Here we show that tDCs are distinct from other well-characterized DCs and conventional DC precursors (pre-cDCs). We demonstrate that tDCs originate from bone marrow progenitors shared with plasmacytoid DCs (pDCs). In the periphery, tDCs contribute to the pool of ESAM

Indexed as

Bone MarrowDendritic CellsAnimalsAntiviral AgentsCell Adhesion MoleculesCell DifferentiationMiceAntiviral AgentsCell Adhesion MoleculesEsam protein, mouse

Identifiers

PMID37414907
PMCPMC10683792
OpenAlexW4383373451

What OpenQuestion holds

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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.