Evidence map›Paper›PMID 32104579›Full record

ReviewClinical & translational immunology2020

Regulatory T cells in solid organ transplantation.

Muhammad Atif, Filomena Conti, Guy Gorochov, Ye Htun Oo, Makoto Miyara

Open access · goldAbstract readReview
In one paragraph

Review in Clinical & translational immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 1 pooled it
4.6field-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

50 citing papers in PubMed, 1 synthesis or guideline pooled it, 80 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Receptor-Mediated SPION Labeling of CD4Nanomaterials (Basel, Switzerland) · 2025
    Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. CD4Scientific reports · 2024
    Article
  19. Donor-Specific Blood Transfusion in Lung Transplantation.Transplant international : official journal of the European Society for Organ Transplantation · 2024
    Review
  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

5 authors at 4 institutions in 2 countries.

Muhammad AtifSorbonne Université Inserm U1135 Centre d'Immunologie et des Maladies Infectieuses (CIMI-Paris) Hôpital Pitié-Salpêtrière AP-HP Paris France.
Filomena ContiUnité de Transplantation Hépatique Hôpital Pitié-Salpêtrière AP-HP Paris France.
Guy GorochovSorbonne Université Inserm U1135 Centre d'Immunologie et des Maladies Infectieuses (CIMI-Paris) Hôpital Pitié-Salpêtrière AP-HP Paris France.
Ye Htun OoCentre for Liver and Gastro Research NIHR Birmingham Biomedical Research Centre University of Birmingham Birmingham UK.
Makoto MiyaraSorbonne Université Inserm U1135 Centre d'Immunologie et des Maladies Infectieuses (CIMI-Paris) Hôpital Pitié-Salpêtrière AP-HP Paris France.
Pitié-Salpêtrière Hospital · FRInserm · FRSorbonne Université · FRUniversity of Birmingham · GB

Funding

Medical Research Council G1002552
6 · The paper itself

Abstract

The induction of graft tolerance remains the holy grail of transplantation. This is important as chronic allograft dysfunction and the side effects of immunosuppression regimens place a major burden on the lives of transplant patients and their healthcare systems. This has mandated the need to understand the immunobiology of graft rejection and identify novel therapeutics. Regulatory T (Treg) cells play an important role in modulating pro-inflammatory microenvironments and maintaining tissue homeostasis. However, there are fundamental unanswered questions regarding Treg cell immunobiology. These cells are a heterogeneous entity with functionally diverse roles. Moreover, the adoption of novel deeper immunophenotyping and genomic sequencing technologies has identified this phenotype and function to be more complex than expected. Hence, a comprehensive understanding of Treg cell heterogeneity is needed to safely and effectively exploit their therapeutic potential. From a clinical perspective, the recent decade has seen different clinical teams commence and complete first-in-man clinical trials utilising Treg cells as an adoptive cellular therapy. In this review, we discuss these trials from a translational perspective with an important focus on safety. Finally, we identify crucial knowledge gaps for future study.

Indexed as

clinical trialFOXP3regulatory T cellssafetytransplantTreg

Identifiers

PMID32104579
PMCPMC7036337
OpenAlexW3007293401

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.