Evidence map›Paper›PMID 27264183›Full record

ArticleCell reports2016

Distinct Transcriptional Programs Control Cross-Priming in Classical and Monocyte-Derived Dendritic Cells.

Carlos G Briseño, Malay Haldar, Nicole M Kretzer, Xiaodi Wu, Derek J Theisen, Wumesh Kc, Vivek Durai, Gary E Grajales-Reyes, Arifumi Iwata, Prachi Bagadia and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 137 papers.

0numbers the graph read from it
0cells of the map it votes in
137citing 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

137 citing papers in PubMed, 201 citations in OpenAlex.

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77 more citing papers are in PubMed but not listed here.

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

12 authors at 2 institutions in 1 country.

Carlos G BriseñoDepartment of Pathology and Immunology, School of Medicine, Washington University in St. Louis, St. Louis, MO 63110, USA.
Malay HaldarDepartment of Pathology and Laboratory Medicine, Perelman School of Medicine and Abramson Family Cancer Research Institute, University of Pennsylvania, Philadelphia, PA 19104, USA.
Nicole M KretzerDepartment of Pathology and Immunology, School of Medicine, Washington University in St. Louis, St. Louis, MO 63110, USA.
Xiaodi WuDepartment of Pathology and Immunology, School of Medicine, Washington University in St. Louis, St. Louis, MO 63110, USA.
Derek J TheisenDepartment of Pathology and Immunology, School of Medicine, Washington University in St. Louis, St. Louis, MO 63110, USA.
Wumesh KcDepartment of Pathology and Immunology, School of Medicine, Washington University in St. Louis, St. Louis, MO 63110, USA.
Vivek DuraiDepartment of Pathology and Immunology, School of Medicine, Washington University in St. Louis, St. Louis, MO 63110, USA.
Gary E Grajales-ReyesDepartment of Pathology and Immunology, School of Medicine, Washington University in St. Louis, St. Louis, MO 63110, USA.
Arifumi IwataDepartment of Pathology and Immunology, School of Medicine, Washington University in St. Louis, St. Louis, MO 63110, USA.
Prachi BagadiaDepartment of Pathology and Immunology, School of Medicine, Washington University in St. Louis, St. Louis, MO 63110, USA.
Theresa L MurphyDepartment of Pathology and Immunology, School of Medicine, Washington University in St. Louis, St. Louis, MO 63110, USA.
Kenneth M MurphyDepartment of Pathology and Immunology, School of Medicine, Washington University in St. Louis, St. Louis, MO 63110, USA; Howard Hughes Medical Institute, School of Medicine, Washington University in St. Louis, St. Louis, MO 63110, USA. Electronic address: kmurphy@wustl.edu.
Washington University in St. Louis · USCancer Research Institute · US

Funding

TRAINING PROGRAM IN IMMUNOLOGY AND IMMUNOGENETICST32AI007163 · NIAID · WASHINGTON UNIVERSITY · PI Kenneth M Murphy, Kodi S Ravichandran · 1985 to 2026
$14.8M
METABOLIC CONTROL OF TISSUE SPECIFIC MACROPHAGE DIFFERENTIATIONK08AI106953 · NIAID · WASHINGTON UNIVERSITY · PI HALDAR, MALAY · 2013 to 2017
$857k
The role of cross-presentation of self-antigens by dendritic cells in type 1 diabetesF30DK108498 · NIDDK · WASHINGTON UNIVERSITY · PI DURAI, VIVEK · 2015 to 2017
$109k
Deciphering CD8 Dendritic Cell Development for the Improvement of VaccineF31CA189491 · NCI · WASHINGTON UNIVERSITY · PI GRAJALES-REYES, GARY E. · 2014 to 2016
$89k
Howard Hughes Medical InstituteNCI NIH HHS F31 CA189491NIAID NIH HHS K08 AI106953NIAID NIH HHS T32 AI007163NIDDK NIH HHS F30 DK108498
6 · The paper itself

Abstract

Both classical DCs (cDCs) and monocyte-derived DCs (Mo-DCs) are capable of cross-priming CD8(+) T cells in response to cell-associated antigens. We found that Ly-6C(hi)TREML4(-) monocytes can differentiate into Zbtb46(+) Mo-DCs in response to granulocyte-macrophage colony-stimulating factor (GM-CSF) and interleukin-4 (IL-4) but that Ly-6C(hi)TREML4(+) monocytes were committed to differentiate into Ly-6C(lo)TREML4(+) monocytes. Differentiation of Zbtb46(+) Mo-DCs capable of efficient cross-priming required both GM-CSF and IL-4 and was accompanied by the induction of Batf3 and Irf4. However, monocytes require IRF4, but not BATF3, to differentiate into Zbtb46(+) Mo-DCs capable of cross-priming CD8(+) T cells. Instead, Irf4(-/-) monocytes differentiate into macrophages in response to GM-CSF and IL-4. Thus, cDCs and Mo-DCs require distinct transcriptional programs of differentiation in acquiring the capacity to prime CD8(+) T cells. These differences may be of consideration in the use of therapeutic DC vaccines based on Mo-DCs.

Indexed as

Transcription, GeneticAnimalsAntigen-Presenting CellsAntigensBasic-Leucine Zipper Transcription FactorsCD8-Positive T-LymphocytesCell DifferentiationCell LineageCross-PrimingDendritic CellsFemaleGranulocyte-Macrophage Colony-Stimulating FactorInterferon Regulatory Factor-4Interferon Regulatory FactorsInterleukin-4MaleAntigensBasic-Leucine Zipper Transcription FactorsGranulocyte-Macrophage Colony-Stimulating FactorInterferon Regulatory Factor-4Interferon Regulatory FactorsInterleukin-4Nr4a1 protein, mouseNuclear Receptor Subfamily 4, Group A, Member 1Receptors, ImmunologicRepressor ProteinsSNFT protein, mouseTreml4 protein, mouse

Identifiers

PMID27264183
PMCPMC4941620
OpenAlexW2412261015

What OpenQuestion holds

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Registered trials

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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.