Evidence map›Paper›PMID 34021046›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2021

MicroRNA-142 Critically Regulates Group 2 Innate Lymphoid Cell Homeostasis and Function.

Luke B Roberts, Geraldine M Jowett, Emily Read, Tomas Zabinski, Rita Berkachy, Murray E Selkirk, Ian Jackson, Umar Niazi, Nelomi Anandagoda, Masatake Araki and 9 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
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  6. Regulation of noncoding RNAs in innate lymphoid cells.Cellular & molecular immunology · 2023
    Article
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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

19 authors at 5 institutions in 2 countries.

Luke B RobertsSchool of Immunology and Microbial Sciences, King's College London, London, United Kingdom.ORCID 0000-0003-1143-304X
Geraldine M JowettCentre for Host-Microbiome Interactions, King's College London, London, United Kingdom.ORCID 0000-0002-8436-6637
Emily ReadCentre for Host-Microbiome Interactions, King's College London, London, United Kingdom.ORCID 0000-0002-0376-2989
Tomas ZabinskiSchool of Immunology and Microbial Sciences, King's College London, London, United Kingdom.
Rita BerkachyDepartment of Life Sciences, Imperial College London, United Kingdom.ORCID 0000-0002-2053-5913
Murray E SelkirkDepartment of Life Sciences, Imperial College London, United Kingdom.ORCID 0000-0002-6274-6014
Ian JacksonSchool of Immunology and Microbial Sciences, King's College London, London, United Kingdom.
Umar NiaziGuy's and St Thomas' National Health Service Foundation Trust and King's College London National Institute for Health Research Biomedical Research Centre Translational Bioinformatics Platform, Guy's Hospital, London, United Kingdom.ORCID 0000-0001-7176-8883
Nelomi AnandagodaSchool of Immunology and Microbial Sciences, King's College London, London, United Kingdom.
Masatake ArakiInstitute of Resource Development and Analysis, Kumamoto University, Kumamoto, Japan.
Kimi ArakiInstitute of Resource Development and Analysis, Kumamoto University, Kumamoto, Japan.
Jagath KasturiarachchiUniversity College London Cancer Institute, University College London, London, United Kingdom.
Chela JamesUniversity College London Cancer Institute, University College London, London, United Kingdom.ORCID 0000-0003-3996-0909
Tariq EnverUniversity College London Cancer Institute, University College London, London, United Kingdom.
Rachael NimmoUniversity College London Cancer Institute, University College London, London, United Kingdom.ORCID 0000-0001-6213-9030
Rita ReisSchool of Immunology and Microbial Sciences, King's College London, London, United Kingdom.ORCID 0000-0002-0182-6694
Jane K HowardSchool of Life Course Sciences, King's College London, London, United Kingdom; and.ORCID 0000-0003-2754-8300
Joana F NevesCentre for Host-Microbiome Interactions, King's College London, London, United Kingdom.ORCID 0000-0001-5842-4162
Graham M LordSchool of Immunology and Microbial Sciences, King's College London, London, United Kingdom; graham.lord@manchester.ac.uk.ORCID 0000-0003-2069-4743
King's College London · GBLondon Cancer · GBImperial College London · GBKumamoto Industrial Research Institute · JPNational Health Service · GB

Funding

British Heart Foundation PG/12/36/29444Cancer Research UK 12796Medical Research Council MR/M003493/1Medical Research Council MR/R024812/1Wellcome Trust 107387/Z/15/ZWellcome Trust 203757/Z/16/AWellcome Trust 204394Wellcome Trust 215027/Z/18/Z
6 · The paper itself

Abstract

Innate lymphoid cells are central to the regulation of immunity at mucosal barrier sites, with group 2 innate lymphoid cells (ILC2s) being particularly important in type 2 immunity. In this study, we demonstrate that microRNA(miR)-142 plays a critical, cell-intrinsic role in the homeostasis and function of ILC2s. Mice deficient for miR-142 expression demonstrate an ILC2 progenitor-biased development in the bone marrow, and along with peripheral ILC2s at mucosal sites, these cells display a greatly altered phenotype based on surface marker expression. ILC2 proliferative and effector functions are severely dysfunctional following

Indexed as

AnimalsHEK293 CellsHomeostasisHumansImmunity, InnateLymphocytesMiceMice, Inbred C57BLMice, KnockoutMicroRNAsMicroRNAsMirn142 microRNA, mouse

Identifiers

PMID34021046
PMCPMC7610861
OpenAlexW3162564363

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.