Evidence map›Paper›PMID 33480151›Full record

ArticleAging cell2021

Interleukin-37 improves T-cell-mediated immunity and chimeric antigen receptor T-cell therapy in aged backgrounds.

Jamie A G Hamilton, Miyoung Y Lee, Rae Hunter, Raira S Ank, Jamie Y Story, Ganesh Talekar, Talia Sisroe, Dov B Ballak, Andrew Fedanov, Christopher C Porter and 5 more

Open access · goldAbstract read
In one paragraph

Article in Aging cell, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 12% 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

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

  1. Pooled it
  2. Review
  3. Interleukin-18 armours antitumour immune effectors.Nature reviews. Immunology · 2026
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  7. Restoration of LAMP2A expression in old mice leads to changes in the T cell compartment that support improved immune function.Proceedings of the National Academy of Sciences of the United States of America · 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

15 authors at 3 institutions in 2 countries.

Jamie A G HamiltonDepartment of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.
Miyoung Y LeeDepartment of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.
Rae HunterDepartment of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.
Raira S AnkDepartment of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.
Jamie Y StoryAflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Atlanta, GA, USA.
Ganesh TalekarDepartment of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.
Talia SisroeEmory University, Atlanta, GA, USA.
Dov B BallakDepartment of Biochemistry and Molecular Genetics, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Andrew FedanovDepartment of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.
Christopher C PorterDepartment of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.
Elan Z EisenmesserDepartment of Biochemistry and Molecular Genetics, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Charles A DinarelloDepartment of Biochemistry and Molecular Genetics, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Sunil S RaikarDepartment of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.
James DeGregoriDepartment of Biochemistry and Molecular Genetics, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Curtis J HenryDepartment of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.ORCID 0000-0002-5523-554X
Emory University · USRadboud University Nijmegen · NLUniversity of Colorado Anschutz Medical Campus · US

Funding

University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR025780 · NCRR · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2008 to 2011
$61.3M
University of Colorado Aging Training GrantT32AG000279 · NIA · UNIVERSITY OF COLORADO DENVER · PI Kerrie Moreau · 2001 to 2026
$10.1M
Yeast-based HTS Assay Technologies for ProteasesR01AI015614 · NIAID · UNIVERSITY OF COLORADO DENVER · PI DINARELLO, CHARLES ANTHONY · 1985 to 2025
$8.5M
Atlanta Pediatric Scholars ProgramK12HD072245 · NICHD · EMORY UNIVERSITY · PI Shari Barkin · 2012 to 2026
$5.5M
Aging-associated alterations in adaptive landscapes and the evolution of leukemiaR01CA180175 · NCI · UNIVERSITY OF COLORADO DENVER · PI DEGREGORI, JAMES V · 2013 to 2018
$1.8M
Gamma delta T-cell immunotherapy for T-cell acute lymphoblastic leukemiaK08CA248962 · NCI · EMORY UNIVERSITY · PI RAIKAR, SUNIL SUDHIR · 2020 to 2024
$1.1M
Dissecting the relationship between declining lymphoid progenitor fitness and agiK01CA160798 · NCI · UNIVERSITY OF COLORADO DENVER · PI HENRY, CURTIS JAMES · 2012 to 2016
$441k
Identifying the missing link in inflammatory signalingR56CA230069 · NCI · UNIVERSITY OF COLORADO DENVER · PI EISENMESSER, ELAN Z · 2019 to 2019
$233k
Interleukin-37: The molecular basis of the atypical interleukin-1 family dimerR03CA219743 · NCI · UNIVERSITY OF COLORADO DENVER · PI EISENMESSER, ELAN Z · 2017 to 2018
$156k
Colorado Clinical & Translational Sciences Institute (CCTSI) P30-CA046934NCI NIH HHS K01 CA160798NCI NIH HHS K08 CA248962NCI NIH HHS P30 CA046934NCI NIH HHS R01 CA180175NCI NIH HHS R03 CA219743NCI NIH HHS R56 CA230069NCRR NIH HHS UL1 RR025780NIAID NIH HHS R01 AI015614NIA NIH HHS T32 AG000279NICHD NIH HHS K12 HD072245NIH HHS 5UL1-RR025780NIH HHS K01 CA160798NIH HHS R01 AI15614NIH HHS R01 CA180175NIH HHS T32 AG000279
6 · The paper itself

Abstract

Aging-associated declines in innate and adaptive immune responses are well documented and pose a risk for the growing aging population, which is predicted to comprise greater than 40 percent of the world's population by 2050. Efforts have been made to improve immunity in aged populations; however, safe and effective protocols to accomplish this goal have not been universally established. Aging-associated chronic inflammation is postulated to compromise immunity in aged mice and humans. Interleukin-37 (IL-37) is a potent anti-inflammatory cytokine, and we present data demonstrating that IL-37 gene expression levels in human monocytes significantly decline with age. Furthermore, we demonstrate that transgenic expression of interleukin-37 (IL-37) in aged mice reduces or prevents aging-associated chronic inflammation, splenomegaly, and accumulation of myeloid cells (macrophages and dendritic cells) in the bone marrow and spleen. Additionally, we show that IL-37 expression decreases the surface expression of programmed cell death protein 1 (PD-1) and augments cytokine production from aged T-cells. Improved T-cell function coincided with a youthful restoration of Pdcd1, Lat, and Stat4 gene expression levels in CD4

Indexed as

AgingCell- and Tissue-Based TherapyAnimalsCell LineFemaleHumansInterleukin-1MaleMiceMice, Inbred BALB CMice, Inbred C57BLMice, TransgenicReceptors, Chimeric AntigenIL37 protein, humanInterleukin-1Receptors, Chimeric AntigenagingCAR T-cellscytokinesinflammationleukemiaPD-1signalingT-cells

Identifiers

PMID33480151
PMCPMC7884049
OpenAlexW3124767772

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.