Evidence map›Paper›PMID 30748096›Full record

ArticleAmerican journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons2019

IL-2 therapy preferentially expands adoptively transferred donor-specific Tregs improving skin allograft survival.

Kulachelvy Ratnasothy, Jacintha Jacob, Sim Tung, Dominic Boardman, Robert Ian Lechler, Alberto Sanchez-Fueyo, Marc Martinez-Llordella, Giovanna Lombardi

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In one paragraph

Article in American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
5.4field-weighted citation impact, top 3% 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, 41 citations in OpenAlex.

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  7. Molecular Engineering of Interleukin-2 for Enhanced Therapeutic Activity in Autoimmune Diseases.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2024
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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

8 authors at 1 institution in 1 country.

Kulachelvy RatnasothyMRC Centre for Transplantation, Peter Gorer Department of Immunobiology, Faculty of Life Sciences & Medicine, King's College London, London, UK.
Jacintha JacobMRC Centre for Transplantation, Peter Gorer Department of Immunobiology, Faculty of Life Sciences & Medicine, King's College London, London, UK.
Sim TungMRC Centre for Transplantation, Peter Gorer Department of Immunobiology, Faculty of Life Sciences & Medicine, King's College London, London, UK.
Dominic BoardmanMRC Centre for Transplantation, Peter Gorer Department of Immunobiology, Faculty of Life Sciences & Medicine, King's College London, London, UK.
Robert Ian LechlerMRC Centre for Transplantation, Peter Gorer Department of Immunobiology, Faculty of Life Sciences & Medicine, King's College London, London, UK.
Alberto Sanchez-FueyoDepartment of Inflammation Biology, MRC Centre for Transplantation, Institute of Liver Studies, Faculty of Life Sciences & Medicine, King's College London, London, UK.
Marc Martinez-LlordellaDepartment of Inflammation Biology, MRC Centre for Transplantation, Institute of Liver Studies, Faculty of Life Sciences & Medicine, King's College London, London, UK.
Giovanna LombardiMRC Centre for Transplantation, Peter Gorer Department of Immunobiology, Faculty of Life Sciences & Medicine, King's College London, London, UK.
King's College London · GB

Funding

British Heart Foundation RG/08/005/25303British Heart Foundation RG/13/12/30395King's Health ParMedical Research Council MR/L008890/1Medical Research Council MR/P007694/1National Institute for Health Research
6 · The paper itself

Abstract

Regulatory T cells (Tregs) have unique immunosuppressive properties and are essential to ensure effective immunoregulation. In animal models, Tregs have been shown to prevent autoimmune disorders and establish transplantation tolerance. Therefore, the prospect of harnessing Tregs, either by increasing their frequency or by conferring allospecificity, has prompted a growing interest in the development of immunotherapies. Here, employing a well-established skin transplant model with a single major histocompatibility complex mismatch, we compared the therapeutic efficacy of adoptively transfer Treg with or without donor specificity and the administration of IL-2 to promote in vivo expansion of Treg. We showed that IL-2 treatment preferentially enhances the proliferation of the allospecific Tregs adoptively transferred in an antigen-dependent manner. In addition, donor-specific Tregs significantly increased the expression of regulatory-related marker, such as CTLA4 and inducible costimulator (ICOS), in the skin allograft and draining lymph nodes compared to endogenous and polyclonal transferred Tregs. Importantly, by combining IL-2 with donor-specific Tregs, but not with polyclonal Tregs, a synergistic effect in prolonging skin allograft survival was observed. Altogether, our data suggest that this combination therapy could provide the appropriate conditions to enhance the immunoregulation of alloimmune responses in clinical transplantation.

Indexed as

Graft SurvivalTissue DonorsAdoptive TransferAllograftsAnimalsDrug SynergismHistocompatibilityImmunotherapyInterleukin-2MiceMice, Inbred CBAMice, TransgenicReceptors, Antigen, T-CellSkin TransplantationT-Lymphocytes, RegulatoryTransplantation, HomologousInterleukin-2Receptors, Antigen, T-Cellantigen presentation/recognitionbasic (laboratory) research/sciencegraft survivalimmune regulationimmunobiologyimmunosuppression/immune modulationorgan transplantation in generalT cell biologytolerancetranslational research/science

Identifiers

PMID30748096
PMCPMC6618286
OpenAlexW2912432695

What OpenQuestion holds

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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.