Evidence map›Paper›PMID 31191558›Full record

ReviewFrontiers in immunology2019

What Makes a pDC: Recent Advances in Understanding Plasmacytoid DC Development and Heterogeneity.

Andrea Musumeci, Konstantin Lutz, Elena Winheim, Anne Barbara Krug

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 88 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
88citing papers in PubMed, 2 pooled it
5.9field-weighted citation impact, top 3% 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

88 citing papers in PubMed, 2 syntheses or guidelines pooled it, 141 citations in OpenAlex.

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  12. HIV Virion Capturing Liposomes for Therapeutic Vaccination.bioRxiv : the preprint server for biology · 2025
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28 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

4 authors at 1 institution in 1 country.

Andrea MusumeciInstitute for Immunology, Biomedical Center, Ludwig-Maximilian-University, Munich, Germany.
Konstantin LutzInstitute for Immunology, Biomedical Center, Ludwig-Maximilian-University, Munich, Germany.
Elena WinheimInstitute for Immunology, Biomedical Center, Ludwig-Maximilian-University, Munich, Germany.
Anne Barbara KrugInstitute for Immunology, Biomedical Center, Ludwig-Maximilian-University, Munich, Germany.
Ludwig-Maximilians-Universität München · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dendritic cells (DCs) are professional antigen presenting cells (APCs) that originate in the bone marrow and are continuously replenished from hematopoietic progenitor cells. Conventional DCs (cDCs) and plasmacytoid DCs (pDCs) are distinguished by morphology and function, and can be easily discriminated by surface marker expression, both in mouse and man. Classification of DCs based on their ontology takes into account their origin as well as their requirements for transcription factor (TF) expression. cDCs and pDCs of myeloid origin differentiate from a common DC progenitor (CDP) through committed pre-DC stages. pDCs have also been shown to originate from a lymphoid progenitor derived IL-7R

Indexed as

AnimalsCell DifferentiationCell PlasticityComputational BiologyDendritic CellsHumansLymphoid Progenitor CellsLymphoid TissueMyeloid Progenitor CellsSignal TransductionDC progenitordendritic cell developmenthematopoiesisheterogeneityplasmacytoid dendritic cellsplasticity

Identifiers

PMID31191558
PMCPMC6548821
OpenAlexW2947420765

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.