Evidence map›Paper›PMID 26819498›Full record

ReviewMediators of inflammation2015

Clinical Use of Tolerogenic Dendritic Cells-Harmonization Approach in European Collaborative Effort.

Anja Ten Brinke, Catharien M U Hilkens, Nathalie Cools, Edward K Geissler, James A Hutchinson, Giovanna Lombardi, Phillip Lord, Birgit Sawitzki, Piotr Trzonkowski, S Marieke Van Ham and 1 more

Registry-linked trialOpen access · goldAbstract readReview
In one paragraph

Review in Mediators of inflammation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02903537 (Tolerance-Induction With Dendritic Cells Treated With Vitamin-D3 and Loaded With Myelin Peptides, in Multiple Sclerosis Patients), which is not on this map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.7field-weighted citation impact, top 6% 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.

NCT02903537 phase1unknown statusnot on this mapstarted 2017, after this paper: background citation

Tolerance-Induction With Dendritic Cells Treated With Vitamin-D3 and Loaded With Myelin Peptides, in Multiple Sclerosis Patients (TOLERVIT-MS)

TypeinterventionalSponsorFundació Institut Germans Trias i PujolRan2017 to 2023Enrolled16ConditionsMultiple Sclerosis, Relapsing-Remitting, Multiple Sclerosis, Chronic ProgressiveArmsAutologous VitD3 tolerogenic monocyte-derived dendritic cells loaded with a pool of myelin peptides (tolDC-VitD3), Interferon-beta
3 · Its place in the literature

Who cites it

37 citing papers in PubMed, 53 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Functional Imaging Using Fluorine (Methods in molecular biology (Clifton, N.J.) · 2021
    Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Regulatory dendritic cells for human organ transplantation.Transplantation reviews (Orlando, Fla.) · 2019
    Review
  15. Summary of the Third International Workshop on Clinical Tolerance.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2019
    Article
  16. Review
  17. Review
  18. Frontiers in immunology · 2019
    Article
  19. Article
  20. 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

11 authors at 9 institutions in 8 countries.

Anja Ten BrinkeDepartment of Immunopathology, Sanquin Blood Supply, Division of Research and Landsteiner Laboratory, Academic Medical Center, University of Amsterdam, Plesmanlaan 125, 1066 CX Amsterdam, Netherlands.
Catharien M U HilkensInstitute of Cellular Medicine, Newcastle University, Newcastle NE2 4HH, UK.
Nathalie CoolsLaboratory of Experimental Hematology, Vaccine & Infectious Disease Institute, Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp University Hospital (UZA), Wilrijkstraat 10, 2650 Edegem, Belgium.
Edward K GeisslerDivision of Experimental Surgery, Department of Surgery, University Hospital Regensburg, Regensburg, 93053 Bavaria, Germany.
James A HutchinsonDivision of Experimental Surgery, Department of Surgery, University Hospital Regensburg, Regensburg, 93053 Bavaria, Germany.
Giovanna LombardiDivision of Transplantation Immunology & Mucosal Biology, MRC Centre for Transplantation, King's College London, Guy's Hospital, London SE1 9RT, UK.
Phillip LordSchool of Computing Science, Newcastle University, Newcastle NE2 4HH, UK.
Birgit SawitzkiInstitute of Medical Immunology, Charité University Medicine, Augustenburger Platz 1, 13353 Berlin, Germany.
Piotr TrzonkowskiDepartment of Clinical Immunology and Transplantology, Medical University of Gdansk, Debinki 7, 80-952 Gdansk, Poland.
S Marieke Van HamDepartment of Immunopathology, Sanquin Blood Supply, Division of Research and Landsteiner Laboratory, Academic Medical Center, University of Amsterdam, Plesmanlaan 125, 1066 CX Amsterdam, Netherlands.
Eva M Martinez-CaceresImmunology Division, Germans Trias i Pujol University Hospital, Department of Cellular Biology, Physiology, and Immunology, Universitat Autònoma Barcelona, Campus Can Ruti, 08916 Barcelona, Spain.
Newcastle University · GBUniversity Hospital Regensburg · DEAcademic Medical Center · NLAntwerp University Hospital · BECharité - Universitätsmedizin Berlin · DEGdańsk Medical University · PLGuy's Hospital · GBUniversitat Autònoma de Barcelona · ESUniversity of Amsterdam · NL

Funding

British Heart Foundation RG/13/12/30395
6 · The paper itself

Abstract

The number of patients with autoimmune diseases and severe allergies and recipients of transplants increases worldwide. Currently, these patients require lifelong administration of immunomodulatory drugs. Often, these drugs are expensive and show immediate or late-occurring severe side effects. Treatment would be greatly improved by targeting the cause of autoimmunity, that is, loss of tolerance to self-antigens. Accumulating knowledge on immune mechanisms has led to the development of tolerogenic dendritic cells (tolDC), with the specific objective to restrain unwanted immune reactions in the long term. The first clinical trials with tolDC have recently been conducted and more tolDC trials are underway. Although the safety trials have been encouraging, many questions relating to tolDC, for example, cell-manufacturing protocols, administration route, amount and frequency, or mechanism of action, remain to be answered. Aiming to join efforts in translating tolDC and other tolerogenic cellular products (e.g., Tregs and macrophages) to the clinic, a European COST (European Cooperation in Science and Technology) network has been initiated-A FACTT (action to focus and accelerate cell-based tolerance-inducing therapies). A FACTT aims to minimize overlap and maximize comparison of tolDC approaches through establishment of minimum information models and consensus monitoring parameters, ensuring that progress will be in an efficient, safe, and cost-effective way.

Indexed as

Adoptive TransferImmune ToleranceAutoimmunityClinical Trials as TopicCooperative BehaviorDendritic CellsEuropeHumans

Identifiers

PMID26819498
PMCPMC4706930
OpenAlexW2261752149

What OpenQuestion holds

Textmetadata
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Read underepoch 390

Registered trials

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.