Evidence map›Paper›PMID 30093707›Full record

ArticleNature communications2018

T cell-intrinsic IL-1R signaling licenses effector cytokine production by memory CD4 T cells.

Aakanksha Jain, Ran Song, Edward K Wakeland, Chandrashekhar Pasare

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 93 papers.

0numbers the graph read from it
0cells of the map it votes in
93citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

93 citing papers in PubMed, 131 citations in OpenAlex.

  1. Trial
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  17. IL1RAJournal of clinical and translational hepatology · 2025
    Article
  18. Review
  19. Article
  20. Review

33 more citing papers are in PubMed but not listed here.

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

4 authors at 2 institutions in 1 country.

Aakanksha JainDepartment of Immunology, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.ORCID http://orcid.org/0000-0001-9602-4987
Ran SongDepartment of Immunology, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
Edward K WakelandDepartment of Immunology, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
Chandrashekhar PasareDepartment of Immunology, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA. chandrashekhar.pasare@cchmc.org.ORCID http://orcid.org/0000-0002-8142-2488
The University of Texas Southwestern Medical Center · USCincinnati Children's Hospital Medical Center · US

Funding

Innate mechanisms of regulation of Th17 responsesR01AI123176 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI Chandrashekhar Pasare · 2017 to 2026
$4.4M
ROLE OF BCAP IN REGULATING INFLAMMATION AND ADAPTIVE IMMUNITYR01AI113125 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI PASARE, CHANDRASHEKHAR · 2015 to 2019
$1.8M
NIAID NIH HHS R01 AI113125NIAID NIH HHS R01 AI123176U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID) AI113125U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID) AI123176
6 · The paper itself

Abstract

Innate cytokines are critical drivers of priming and differentiation of naive CD4 T cells, but their functions in memory T cell response are largely undefined. Here we show that IL-1 acts as a licensing signal to permit effector cytokine production by pre-committed Th1 (IFN-γ), Th2 (IL-13, IL-4, and IL-5) and Th17 (IL-17A, IL-17F, and IL-22) lineage cells. This licensing function of IL-1 is conserved across effector CD4 T cells generated by diverse immunological insults. IL-1R signaling stabilizes cytokine transcripts to enable productive and rapid effector functions. We also demonstrate that successful lineage commitment does not translate into productive effector functions in the absence of IL-1R signaling. Acute abrogation of IL-1R signaling in vivo results in reduced IL-17A production by intestinal Th17 cells. These results extend the role of innate cytokines beyond CD4 T cell priming and establish IL-1 as a licensing signal for memory CD4 T cell function.

Indexed as

Immunologic MemoryAnimalsCD4-Positive T-LymphocytesCell LineageCell ProliferationCytokinesDendritic CellsHumansHyaluronan ReceptorsInterleukin-17Interleukin-18Interleukin-1betaL-SelectinMiceMice, Inbred C57BLMice, TransgenicCD44 protein, humanCd44 protein, mouseCytokinesHyaluronan ReceptorsIL17A protein, humanIl17a protein, mouseIL1R1 protein, humanIL1R1 protein, mouseInterleukin-17Interleukin-18Interleukin-1betaL-SelectinMYD88 protein, humanMyd88 protein, mouseMyeloid Differentiation Factor 88Receptors, Interleukin-1 Type IRNA, Messenger

Identifiers

PMID30093707
PMCPMC6085393
OpenAlexW2886350482

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.