Evidence map›Paper›PMID 35148827›Full record

ArticleImmunity2022

Interferon-β acts directly on T cells to prolong allograft survival by enhancing regulatory T cell induction through Foxp3 acetylation.

Francisco Fueyo-González, Mitchell McGinty, Mehek Ningoo, Lisa Anderson, Chiara Cantarelli, Andrea Angeletti, Markus Demir, Inés Llaudó, Carolina Purroy, Nada Marjanovic and 5 more

Open access · greenAbstract read
In one paragraph

Article in Immunity, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 7% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

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  11. Endogenous retroelements promote tolerance to dietary antigens.bioRxiv : the preprint server for biology · 2025
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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

15 authors at 6 institutions in 4 countries.

Francisco Fueyo-GonzálezDivision of Nephrology, Department of Medicine, Translational Transplant Research Center, Icahn School of Medicine at Mount Sinai, New York City, NY, USA; Immunology Institute Icahn School of Medicine at Mount Sinai, New York City, NY, USA.
Mitchell McGintyCarter Immunology Center, University of Virginia, Charlottesville, VA 22903, USA.
Mehek NingooDivision of Nephrology, Department of Medicine, Translational Transplant Research Center, Icahn School of Medicine at Mount Sinai, New York City, NY, USA; Immunology Institute Icahn School of Medicine at Mount Sinai, New York City, NY, USA.
Lisa AndersonDivision of Nephrology, Department of Medicine, Translational Transplant Research Center, Icahn School of Medicine at Mount Sinai, New York City, NY, USA; Immunology Institute Icahn School of Medicine at Mount Sinai, New York City, NY, USA.
Chiara CantarelliUO Nefrologia, Azienda Ospedaliero-Universitaria Parma, Parma, Italy.
Andrea AngelettiDivision of Nephrology, Dialysis, Transplantation, IRCCS Giannina Gaslini, Genoa, Italy.
Markus DemirDepartment of Anesthesiology, University of Cologne, Cologne, Germany.
Inés LlaudóDivision of Nephrology, Department of Medicine, Translational Transplant Research Center, Icahn School of Medicine at Mount Sinai, New York City, NY, USA; Immunology Institute Icahn School of Medicine at Mount Sinai, New York City, NY, USA.
Carolina PurroyDepartment of Nephrology, Complejo Hospitalario de Navarra, Navarra, Spain.
Nada MarjanovicImmunology Institute Icahn School of Medicine at Mount Sinai, New York City, NY, USA; Department of Neurology, Icahn School of Medicine at Mount Sinai, New York City, NY, USA.
David HejaDivision of Nephrology, Department of Medicine, Translational Transplant Research Center, Icahn School of Medicine at Mount Sinai, New York City, NY, USA; Immunology Institute Icahn School of Medicine at Mount Sinai, New York City, NY, USA.
Stuart C SealfonImmunology Institute Icahn School of Medicine at Mount Sinai, New York City, NY, USA; Department of Neurology, Icahn School of Medicine at Mount Sinai, New York City, NY, USA.
Peter S HeegerDivision of Nephrology, Department of Medicine, Translational Transplant Research Center, Icahn School of Medicine at Mount Sinai, New York City, NY, USA; Immunology Institute Icahn School of Medicine at Mount Sinai, New York City, NY, USA.
Paolo CravediDivision of Nephrology, Department of Medicine, Translational Transplant Research Center, Icahn School of Medicine at Mount Sinai, New York City, NY, USA; Immunology Institute Icahn School of Medicine at Mount Sinai, New York City, NY, USA.
Miguel FribourgDivision of Nephrology, Department of Medicine, Translational Transplant Research Center, Icahn School of Medicine at Mount Sinai, New York City, NY, USA; Immunology Institute Icahn School of Medicine at Mount Sinai, New York City, NY, USA. Electronic address: miguel.fribourg@mssm.edu.
Icahn School of Medicine at Mount Sinai · USCarter Center · USComplejo Hospitalario de Navarra · ESIstituto Giannina Gaslini · ITOspedale di Parma · ITUniversity of Cologne · DE

Funding

Project I: Immunity to Influenza in Primary Lung Epithelial CellsU19AI117873 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI HAYOT, FERNAND · 2015 to 2019
$8.6M
Erythropoietin mediated immunoregulation in murine lupus nephritisR01AI132949 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CRAVEDI, PAOLO · 2018 to 2022
$2.1M
Interferon-beta in transplantR01AI141710 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI FRIBOURG, MIGUEL · 2018 to 2022
$2.1M
Interferon-beta trans-signaling in transplantR56AI141710 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI FRIBOURG, MIGUEL · 2023 to 2023
$381k
NIAID NIH HHS R01 AI132949NIAID NIH HHS R01 AI141710NIAID NIH HHS R56 AI141710NIAID NIH HHS U19 AI117873
6 · The paper itself

Abstract

Type I interferons (IFNs) are pleiotropic cytokines with potent antiviral properties that also promote protective T cell and humoral immunity. Paradoxically, type I IFNs, including the widely expressed IFNβ, also have immunosuppressive properties, including promoting persistent viral infections and treating T-cell-driven, remitting-relapsing multiple sclerosis. Although associative evidence suggests that IFNβ mediates these immunosuppressive effects by impacting regulatory T (Treg) cells, mechanistic links remain elusive. Here, we found that IFNβ enhanced graft survival in a Treg-cell-dependent murine transplant model. Genetic conditional deletion models revealed that the extended allograft survival was Treg cell-mediated and required IFNβ signaling on T cells. Using an in silico computational model and analysis of human immune cells, we found that IFNβ directly promoted Treg cell induction via STAT1- and P300-dependent Foxp3 acetylation. These findings identify a mechanistic connection between the immunosuppressive effects of IFNβ and Treg cells, with therapeutic implications for transplantation, autoimmunity, and malignancy.

Indexed as

Interferon-betaT-Lymphocytes, RegulatoryAcetylationAllograftsAnimalsForkhead Transcription FactorsGraft SurvivalHumansMiceForkhead Transcription FactorsFOXP3 protein, humanFoxp3 protein, mouseInterferon-betaacetylationCTLA-4 IgFoxp3interferon-betaregulatory T cellstransplant

Identifiers

PMID35148827
PMCPMC8917088
OpenAlexW4211252841

What OpenQuestion holds

Textmetadata
LicenceTDM
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.