Evidence map›Paper›PMID 41275417›Full record

ReviewImmunological reviews2025

Bridging pDCs and cDCs: The Identity of Transitional Dendritic Cells.

Juliana Idoyaga, Hai Ni, Raul A Maqueda-Alfaro

Abstract readReview
In one paragraph

Review in Immunological reviews, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
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

3 authors.

Juliana IdoyagaDepartment of Pharmacology, University of California San Diego School of Medicine, La Jolla, California, USA.ORCID https://orcid.org/0000-0002-4430-8862
Hai NiDepartment of Pharmacology, University of California San Diego School of Medicine, La Jolla, California, USA.
Raul A Maqueda-AlfaroDepartment of Pharmacology, University of California San Diego School of Medicine, La Jolla, California, USA.

Funding

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
Novel transcription factors modulating the development and function of pDCs and pDC-related cellsR21AI163775 · NIAID · STANFORD UNIVERSITY · PI IDOYAGA, JULIANA · 2021 to 2022
$437k
National Institutes of Health, USA AI158808National Institutes of Health, USA AI163775NIAID NIH HHS R01 AI158808NIAID NIH HHS R21 AI163775
6 · The paper itself

Abstract

Transitional dendritic cells (tDCs) have emerged as a compelling addition to the dendritic cell (DC) network-a hybrid subset that bridges plasmacytoid (pDC) and conventional (cDC) lineages, particularly conventional type 2 DCs (cDC2s). First identified through high-dimensional single-cell profiling, tDCs combine features of both pDCs and cDC2s yet follow a distinct developmental trajectory with unique effector functions. Although ontogenetically related to pDCs, tDCs do not produce type I interferon but instead mount a robust IL-1β response upon pathogen sensing, positioning them as rapid initiators of innate inflammation. tDCs also mirror cDC2s in their ability to capture antigen and prime naïve CD4

Indexed as

Dendritic CellsAnimalsAntigen PresentationCell DifferentiationHumansInflammationInterleukin-1betaSingle-Cell AnalysisInterleukin-1betacDC2AcDC2Bconventional dendritic cells (cDC)IL‐1βplasmacytoid dendritic cells (pDCs)transitional dendritic cells (tDCs)

Identifiers

PMID41275417
PMCPMC12640671

What Socratic 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 Socratic graph.