Evidence map›Paper›PMID 34375446›Full record

ReviewEuropean journal of immunology2021

Advances in Liver Transplantation: where are we in the pursuit of transplantation tolerance?

Niloufar Safinia, Trishan Vaikunthanathan, Robert Ian Lechler, Alberto Sanchez-Fueyo, Giovanna Lombardi

Open access · hybridFull text readReview
In one paragraph

Review in European journal of immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
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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 2 institutions in 2 countries.

Niloufar SafiniaDivision of Transplantation Immunology & Mucosal Biology, King's College London, London, UK.
Trishan VaikunthanathanDepartment of Inflammation Biology, King's College London, London, UK.
Robert Ian LechlerDivision of Transplantation Immunology & Mucosal Biology, King's College London, London, UK.
Alberto Sanchez-FueyoDepartment of Inflammation Biology, King's College London, London, UK.
Giovanna LombardiDivision of Transplantation Immunology & Mucosal Biology, King's College London, London, UK.
King's College London · GBHealth First · US

Funding

Department of HealthMedical Research Council G1002000Medical Research Council MC_PC_15108Medical Research Council MC_PC_19041Wellcome Trust 211113/Z/18/Z
6 · The paper itself

Abstract

Liver transplantation is the ultimate treatment option for end-stage liver disease. Breakthroughs in surgical practice and immunosuppression have seen considerable advancements in survival after transplantation. However, the intricate management of immunosuppressive regimens, balancing desired immunological quiescence while minimizing toxicity has proven challenging. Diminishing improvements in long-term morbidity and mortality have been inextricably linked with the protracted use of these medications. As such, there is now enormous interest to devise protocols that will allow us to minimize or completely withdraw immunosuppressants after transplantation. Immunosuppression withdrawal trials have proved the reality of tolerance following liver transplantation, however, without intervention will only occur after several years at the risk of potential cumulative immunosuppression-related morbidity. Focus has now been directed at accelerating this phenomenon through tolerance-inducing strategies. In this regard, efforts have seen the use of regulatory cell immunotherapy. Here we focus particularly on regulatory T cells, discussing preclinical data that propagated several clinical trials of adoptive cell therapy in liver transplantation. Furthermore, we describe efforts to further optimize the specificity and survival of regulatory cell therapy guided by concurrent immunomonitoring studies and the development of novel technologies including chimeric antigen receptors and co-administration of low-dose IL-2.

Indexed as

Transplantation ImmunologyAnimalsCell CommunicationClinical Studies as TopicClinical Trials as TopicCombined Modality TherapyHumansImmunomodulationLiverLiver DiseasesLiver TransplantationModels, AnimalOrgan SpecificityT-Lymphocytes, RegulatoryT-Lymphocyte SubsetsTransplantation Toleranceimmunosuppression withdrawalimmunotherapyliver transplantationregulatory T cellstolerance

Identifiers

PMID34375446
PMCPMC10015994
OpenAlexW3189986953

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read17
identifiers read16
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.