Evidence map›Paper›PMID 41210169›Full record

ArticleMolecular therapy. Methods & clinical development2025

Protocol of generation of tolerogenic dendritic cells affects their transcriptional and metabolic profiles leading to specific tolerogenic functions.

Maaike Suuring, Giada Amodio, Mathieu Rouel, Axel Raux, Thomas Delhaye, Anne-Lise Royer, Chloé Cloteau, Denisia Lavercan, David Rondeau, Elise Chiffoleau and 4 more

Abstract read
In one paragraph

Article in Molecular therapy. Methods & clinical development, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Tailoring monocyte-derived tolerogenic cell therapies to the needs; what's in a name?Molecular therapy. Methods & clinical development · 2025
    Article
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

14 authors.

Maaike SuuringNantes Université, INSERM, Center for Research in Transplantation and Translational Immunology, UMR 1064, ITUN, 44000 Nantes, France.
Giada AmodioMechanisms of Peripheral Tolerance Unit, San Raffaele Telethon Institute for Gene Therapy (SR-TIGET), IRCCS San Raffaele Scientific Institute, 20132 Milan, Italy.
Mathieu RouelNantes Université, INSERM, Center for Research in Transplantation and Translational Immunology, UMR 1064, ITUN, 44000 Nantes, France.
Axel RauxMELISA Core Facility, Oniris, LABERCA INRΑE, 44307 Nantes, France.
Thomas DelhayeUniversity Rennes, CNRS, Institut d'Electronique et des Technologies du numéRique - UMR 6164, SM Platform, 35000 Rennes, France.
Anne-Lise RoyerMELISA Core Facility, Oniris, LABERCA INRΑE, 44307 Nantes, France.
Chloé CloteauNantes Université, CNRS, INSERM, L'institut du Thorax, 44000 Nantes, France.
Denisia LavercanNantes Université, CHU Nantes, Inserm, CNRS, SFR Santé, Inserm UMS 016, CNRS UMS 3556, 44000 Nantes, France.
David RondeauUniversity Rennes, CNRS, Institut d'Electronique et des Technologies du numéRique - UMR 6164, SM Platform, 35000 Rennes, France.
Elise ChiffoleauNantes Université, INSERM, Center for Research in Transplantation and Translational Immunology, UMR 1064, ITUN, 44000 Nantes, France.
Francesca Santoni de SioMechanisms of Peripheral Tolerance Unit, San Raffaele Telethon Institute for Gene Therapy (SR-TIGET), IRCCS San Raffaele Scientific Institute, 20132 Milan, Italy.
Mikaël CroyalNantes Université, CNRS, INSERM, L'institut du Thorax, 44000 Nantes, France.
Silvia GregoriMechanisms of Peripheral Tolerance Unit, San Raffaele Telethon Institute for Gene Therapy (SR-TIGET), IRCCS San Raffaele Scientific Institute, 20132 Milan, Italy.
Aurélie MoreauNantes Université, INSERM, Center for Research in Transplantation and Translational Immunology, UMR 1064, ITUN, 44000 Nantes, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell therapy is a promising approach for inducing tolerance and thus reducing the use of immunosuppressive drugs in several immune-mediated conditions. Tolerogenic dendritic cells (tolDCs) regulate antigen-specific tolerance and control the immune response, making them an interesting candidate for cell therapy. Over the last years, different human tolDCs have been generated

Indexed as

cell therapyclinical applicationimmunoregulationmetabolismtolerogenic dendritic cellstranscriptome

Identifiers

PMID41210169
PMCPMC12589953

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.