Evidence map›Paper›PMID 37269733›Full record

ReviewMolecular immunology2023

Plasmacytoid dendritic cells: A dendritic cell in disguise.

Rebeca Arroyo Hornero, Juliana Idoyaga

Open access · hybridAbstract readReview
In one paragraph

Review in Molecular immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
5.4field-weighted citation impact, top 4% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. DNA fromMicroorganisms · 2025
    Article
  15. Human LY9 governs CD4Science immunology · 2025
    Article
  16. Mixed Leukocyte Reaction Using Human Plasmacytoid Dendritic Cells and CD4Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  17. Article
  18. Article
  19. Article
  20. 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

2 authors at 1 institution in 1 country.

Rebeca Arroyo HorneroMicrobiology & Immunology Department, and Immunology Program, Stanford University School of Medicine, Stanford, CA 94305, USA.
Juliana IdoyagaMicrobiology & Immunology Department, and Immunology Program, Stanford University School of Medicine, Stanford, CA 94305, USA. Electronic address: jidoyaga@stanford.edu.
Stanford University · US

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
NIAID NIH HHS R01 AI158808NIAID NIH HHS R21 AI163775
6 · The paper itself

Abstract

Since their discovery, the identity of plasmacytoid dendritic cells (pDCs) has been at the center of a continuous dispute in the field, and their classification as dendritic cells (DCs) has been recently re-challenged. pDCs are different enough from the rest of the DC family members to be considered a lineage of cells on their own. Unlike the exclusive myeloid ontogeny of cDCs, pDCs may have dual origin developing from myeloid and lymphoid progenitors. Moreover, pDCs have the unique ability to quickly secrete abundant levels of type I interferon (IFN-I) in response to viral infections. In addition, pDCs undergo a differentiation process after pathogen recognition that allows them to activate T cells, a feature that has been shown to be independent of presumed contaminating cells. Here, we aim to provide an overview of the historic and current understanding of pDCs and argue that their classification as either lymphoid or myeloid may be an oversimplification. Instead, we propose that the capacity of pDCs to link the innate and adaptive immune response by directly sensing pathogens and activating adaptive immune responses justify their inclusion within the DC network.

Indexed as

Adaptive ImmunityT-LymphocytesCell DifferentiationDendritic CellsImmunity, HumoralAntigen presentationPlasmacytoid dendritic cellsTransitional dendritic cellsType I interferon

Identifiers

PMID37269733
PMCPMC10625168
OpenAlexW4379055367

What OpenQuestion holds

Textmetadata
LicenceTDM
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.