Evidence map›Paper›PMID 31607369›Full record

ReviewAdvances in immunology2019

Models of dendritic cell development correlate ontogeny with function.

David A Anderson, Kenneth M Murphy

Abstract readReview
In one paragraph

Review in Advances in immunology, 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
–field-weighted citation impact
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.

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  14. OMV Vaccines and the Role of TLR Agonists in Immune Response.International journal of molecular sciences · 2020
    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

2 authors.

David A AndersonDepartment of Pathology and Immunology, School of Medicine, Washington University in St. Louis, St. Louis, MO, United States. Electronic address: davidandersoniii@wustl.edu.
Kenneth M MurphyDepartment of Pathology and Immunology, School of Medicine, Washington University in St. Louis, St. Louis, MO, United States; Howard Hughes Medical Institute, School of Medicine, Washington University in St. Louis, St. Louis, MO, United States.

Funding

Function of Wdfy4 in cross-presentation and immunityR01AI150297 · NIAID · WASHINGTON UNIVERSITY · PI MURPHY, KENNETH M · 2019 to 2023
$2.5M
The regulation of dendritic cell function by LMYC at steady state and during immune responses to cancerF31CA228240 · NCI · WASHINGTON UNIVERSITY · PI ANDERSON, DAVID ALEXANDER · 2018 to 2020
$93k
NCI NIH HHS F31 CA228240NIAID NIH HHS R01 AI150297
6 · The paper itself

Abstract

Rapid advances have been made to uncover the mechanisms that regulate dendritic cell (DC) development, and in turn, how models of development can be employed to define dendritic cell function. Models of DC development have been used to define the unique functions of DC subsets during immune responses to distinct pathogens. More recently, models of DC function have expanded to include their homeostatic and inflammatory physiology, modes of communication with various innate and adaptive immune lineages, and specialized functions across different lymphoid organs. New models of DC development call for revisions of previously accepted paradigms with respect to the ontogeny of plasmacytoid DC (pDC) and classical DC (cDC) subsets. By far, development of the cDC1 subset is best understood, and models have now been developed that can separate deficiencies in development from deficiencies in function. Such models are lacking for pDCs and cDC2s, limiting the depth of our understanding of their unique and essential roles during immune responses. If novel immunotherapies aim to harness the functions of human DCs, understanding of DC development will be essential to develop models DC function. Here we review emerging models of DC development and function.

Indexed as

AnimalsCD8-Positive T-LymphocytesCell DifferentiationCytokinesDendritic CellsHumansInhibitor of Differentiation Protein 2Interferon Regulatory Factor-8Interferon Regulatory FactorsLymphoid Progenitor CellsMiceModels, ImmunologicalMyeloid Progenitor CellsZinc Finger E-box Binding Homeobox 2CytokinesInhibitor of Differentiation Protein 2Interferon Regulatory Factor-8Interferon Regulatory FactorsZinc Finger E-box Binding Homeobox 2Dendritic cellsDevelopmentMaturationTranscription factors

Identifiers

PMID31607369
PMCPMC10931540

What OpenQuestion holds

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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.