Evidence map›Paper›PMID 35180378›Full record

ArticleImmunity2022

Clonal lineage tracing reveals shared origin of conventional and plasmacytoid dendritic cells.

Jue Feng, Joseph N Pucella, Geunhyo Jang, Marcela Alcántara-Hernández, Samik Upadhaya, Nicholas M Adams, Alireza Khodadadi-Jamayran, Colleen M Lau, Marlon Stoeckius, Stephanie Hao and 4 more

Open access · greenAbstract read
In one paragraph

Article in Immunity, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
7.5field-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

61 citing papers in PubMed, 93 citations in OpenAlex.

  1. IL-17D reprograms CD93Cellular & molecular immunology · 2026
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  15. Myeloid cells in chronic liver inflammation.Cellular & molecular immunology · 2025
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  18. RORγt eTACs mediate oral tolerance and Treg induction.The Journal of experimental medicine · 2025
    Article
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1 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 3 institutions in 1 country.

Jue FengDepartment of Pathology, New York University Grossman School of Medicine, New York, NY 10016, USA. Electronic address: jue.feng@nyulangone.org.
Joseph N PucellaDepartment of Pathology, New York University Grossman School of Medicine, New York, NY 10016, USA.
Geunhyo JangDepartment of Pathology, New York University Grossman School of Medicine, New York, NY 10016, USA.
Marcela Alcántara-HernándezDepartment of Microbiology & Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA; Immunology Program, Stanford University School of Medicine, Stanford, CA 94305, USA.
Samik UpadhayaDepartment of Pathology, New York University Grossman School of Medicine, New York, NY 10016, USA.
Nicholas M AdamsDepartment of Pathology, New York University Grossman School of Medicine, New York, NY 10016, USA.
Alireza Khodadadi-JamayranDepartment of Pathology, New York University Grossman School of Medicine, New York, NY 10016, USA; Applied Bioinformatics Laboratories, New York University Grossman School of Medicine, New York, NY 10016, USA.
Colleen M LauDepartment of Pathology, New York University Grossman School of Medicine, New York, NY 10016, USA.
Marlon StoeckiusTechnology Innovation Laboratory, New York Genome Center, New York, NY 10013, USA.
Stephanie HaoTechnology Innovation Laboratory, New York Genome Center, New York, NY 10013, USA.
Peter SmibertTechnology Innovation Laboratory, New York Genome Center, New York, NY 10013, USA.
Aristotelis TsirigosDepartment of Pathology, New York University Grossman School of Medicine, New York, NY 10016, USA; Applied Bioinformatics Laboratories, New York University Grossman School of Medicine, New York, NY 10016, USA.
Juliana IdoyagaDepartment of Microbiology & Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA; Immunology Program, Stanford University School of Medicine, Stanford, CA 94305, USA.
Boris ReizisDepartment of Pathology, New York University Grossman School of Medicine, New York, NY 10016, USA. Electronic address: boris.reizis@nyulangone.org.
New York University · USNew York Genome Center · USStanford University · US

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Richard Lewis Possemato · 1985 to 2026
$83.1M
TRAINING PROGRAM IN MOLECULAR ONCOLOGY &IMMUNOLOGYT32CA009161 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI CARROLL, WILLIAM L., LEVY, DAVID E · 1985 to 2020
$13.3M
Molecular Control of Plasmacytoid Dendritic Cell Development and FunctionR37AI072571 · NIAID · UNIVERSITY OF CHICAGO · PI Boris Reizis · 2018 to 2026
$5.3M
Training Program in Immunology and Inflammation.T32AI100853 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Susan Ruth Schwab · 2012 to 2026
$4.5M
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
Dissecting the aging of hematopoietic stem cells by genetic tracing in vivoR01AG049074 · NIA · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI REIZIS, BORIS · 2015 to 2019
$1.7M
Analyzing dendritic cell development by inducible lineage tracingR21AI115382 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI REIZIS, BORIS · 2015 to 2016
$466k
Studying immune development at single-cell resolution by DNA barcodingR21AI128730 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI REIZIS, BORIS · 2017 to 2018
$466k
Kinetic Characterization of Hematopoietic Stem Cell Differentiation During Homeostasis And Pathological ConditionsF32HL145997 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI PUCELLA, JOSEPH NICHOLAS · 2019 to 2021
$176k
NCI NIH HHS P30 CA016087NCI NIH HHS T32 CA009161NHLBI NIH HHS F32 HL145997NIAID NIH HHS R01 AI072571NIAID NIH HHS R01 AI158808NIAID NIH HHS R21 AI115382NIAID NIH HHS R21 AI128730NIAID NIH HHS R37 AI072571NIAID NIH HHS T32 AI100853NIA NIH HHS R01 AG049074
6 · The paper itself

Abstract

Developmental origins of dendritic cells (DCs) including conventional DCs (cDCs, comprising cDC1 and cDC2 subsets) and plasmacytoid DCs (pDCs) remain unclear. We studied DC development in unmanipulated adult mice using inducible lineage tracing combined with clonal DNA "barcoding" and single-cell transcriptome and phenotype analysis (CITE-seq). Inducible tracing of Cx3cr1

Indexed as

B-LymphocytesDendritic CellsAnimalsCell CountChoreaHematopoietic Stem CellsMiceconventional dendritic cellshematopoietic progenitorshematopoietic stem cellslineage tracingplasmacytoid dendritic cells

Identifiers

PMID35180378
PMCPMC9344860
OpenAlexW4212776244

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.