Evidence map›Paper›PMID 30294962›Full record

ReviewImmunological reviews2018

Type 2 innate lymphoid cells in the induction and resolution of tissue inflammation.

Antonia Wallrapp, Samantha J Riesenfeld, Patrick R Burkett, Vijay K Kuchroo

Open access · greenAbstract readReview
In one paragraph

Review in Immunological reviews, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

37 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
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  15. Review
  16. Neuroimmune Interactions in the Intestine.Annual review of immunology · 2024
    Review
  17. Article
  18. Review
  19. International journal of molecular sciences · 2023
    Article
  20. Review
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.

Antonia WallrappEvergrande Center for Immunologic Diseases, Harvard Medical School and Brigham & Women's Hospital, Boston, Massachusetts.
Samantha J RiesenfeldKlarman Cell Observatory, Broad Institute of MIT and Harvard, Cambridge, Massachusetts.
Patrick R BurkettEvergrande Center for Immunologic Diseases, Harvard Medical School and Brigham & Women's Hospital, Boston, Massachusetts.
Vijay K KuchrooEvergrande Center for Immunologic Diseases, Harvard Medical School and Brigham & Women's Hospital, Boston, Massachusetts.ORCID 0000-0001-7177-2110
Brigham and Women's Hospital · USBroad Institute · US

Funding

Role of Negative Costimulation in Regulation of AutoimmunityP01AI039671 · NIAID · YALE UNIVERSITY · PI David A. Hafler · 1996 to 2026
$51.7M
Transgenic/KnockoutP01AI056299 · NIAID · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI BLAZAR, BRUCE R · 2003 to 2023
$42.5M
TCR recognition of MHC class II peptide compexes in multiple sclerosisP01AI045757 · NIAID · DANA-FARBER CANCER INSTITUTE · PI KUCHROO, VIJAY K., LOVE, JOHN CHRISTOPHER · 1999 to 2017
$22.8M
Transgenic / Knock-out mouse coreP01AI073748 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI BEHAR, SAMUEL M · 2008 to 2019
$17.1M
Transcriptional regulations of effector and regulatory T cells in EAEP01NS076410 · NINDS · BRIGHAM AND WOMEN'S HOSPITAL · PI KUCHROO, VIJAY K. · 2013 to 2017
$5.6M
In situ transcriptional analysis of brain circuits at single cell resolutionR01MH111502 · NIMH · HARVARD UNIVERSITY · PI DULAC, CATHERINE, REGEV, AVIV · 2016 to 2018
$4.6M
T CELL RESPONSE TO MYELIN PROTEOLIPID PROTEINR01NS030843 · NINDS · BRIGHAM AND WOMEN'S HOSPITAL · PI KUCHROO, VIJAY K. · 1998 to 2019
$4.1M
Neuroimmune interactions regulate development of allergic inflammationR01AI139536 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI KUCHROO, VIJAY K. · 2018 to 2022
$2.9M
CLEC-2/Pdpn Mediated Regulation of Airway InflammationK08AI123516 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI BURKETT, PATRICK RYLAND · 2016 to 2019
$744k
NIAID NIH HHS K08 AI123516NIAID NIH HHS P01 AI039671NIAID NIH HHS P01 AI045757NIAID NIH HHS P01 AI056299NIAID NIH HHS P01 AI073748NIAID NIH HHS R01 AI139536NIH HHS 1K08AI123516NIH HHS 1R01 MH111502NIH HHS R01 AI139536NIMH NIH HHS R01 MH111502NINDS NIH HHS P01 NS076410NINDS NIH HHS R01 NS030843
6 · The paper itself

Abstract

Type 2 immunity against pathogens is tightly regulated to ensure appropriate inflammatory responses that clear infection and prevent excessive tissue damage. Recent research has shown that type 2 innate lymphoid cells (ILC2s) contribute to steady-state tissue integrity and exert tissue-specific functions. However, upon exposure to inflammatory stimuli, they also initiate and amplify type 2 inflammation by inducing mucus production, eosinophilia, and Th2 differentiation. In this review, we discuss the regulation of ILC2 activation by transcription factors and metabolic pathways, as well as by extrinsic signals such as cytokines, lipid mediators, hormones, and neuropeptides. We also review recent discoveries about ILC2 plasticity and heterogeneity in different tissues, as revealed partly through single-cell RNA sequencing of transcriptional responses to various stimuli. Understanding the tissue-specific pathways that regulate ILC2 diversity and function is a critical step in the development of potential therapies for allergic diseases.

Indexed as

AnimalsCell DifferentiationCytokinesHigh-Throughput Nucleotide SequencingHumansImmunity, InnateInflammationLymphocyte ActivationSingle-Cell AnalysisTh2 CellsCytokinesdisease resolutioninnate immunityinnate lymphoid cellsmucosal immunologyneuroimmunologytype 2 inflammation

Identifiers

PMID30294962
PMCPMC7370855
OpenAlexW2896268091

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.