Evidence map›Paper›PMID 32609880›Full record

ReviewImmunology2020

Role of myeloid cells in the regulation of group 2 innate lymphoid cell-mediated allergic inflammation.

Aihua Lei, Yumei He, Qiong Yang, Xiaofang Li, Ranhui Li

Abstract readReview
In one paragraph

Review in Immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. 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

5 authors.

Aihua LeiInstitute of Pathogenic Biology, Hengyang Medical College, Hunan Provincial Key Laboratory for Special Pathogens Prevention and Control, Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study, University of South China, Hengyang, China.ORCID 0000-0002-1498-5520
Yumei HeDepartment of Immunology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Qiong YangChronic Disease Laboratory, Institutes for Life Sciences and School of Medicine, South China University of Technology, Guangzhou, China.
Xiaofang LiInstitute of Pathogenic Biology, Hengyang Medical College, Hunan Provincial Key Laboratory for Special Pathogens Prevention and Control, Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study, University of South China, Hengyang, China.
Ranhui LiInstitute of Pathogenic Biology, Hengyang Medical College, Hunan Provincial Key Laboratory for Special Pathogens Prevention and Control, Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study, University of South China, Hengyang, China.

Funding

Foundation of Hunan Provincial Key Laboratory for Special Pathogens Prevention and Control 2014-5Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study 2015-351National Natural Science Foundation of China 81800031National Natural Science Foundation of Guangdong 2019A1515011435Natural Science Foundation of Guangdong Province 2016A030310182Natural Science Foundation of Guangdong Province 2018A030313648Natural Science Foundation of Hunan Province 2020JJ4521Science and Technology Program of Guangzhou 201904010073
6 · The paper itself

Abstract

Group 2 innate lymphoid cells (ILC2s) are an important component of the innate immune system that execute important effector functions at barrier surfaces, such as lung and skin. Like T helper type 2 cells, ILC2s are able to release high amounts of type 2 cytokines that are essential in inducing allergic inflammation and eliminating helminth infections. The past few years have contributed to our better understanding of the interactions between ILC2s and other cells of the immune system via soluble factors or in a cell-cell contact manner. Myeloid cells, including mononuclear leukocytes and polymorphonuclear leukocytes, are excellent sensors of tissue damage and infection and can influence ILC2 responses in the process of allergic inflammation. In this review, we summarize recent insights on how myeloid cell subsets regulate ILC2 activation with focus on soluble factors in the context of allergic inflammation.

Indexed as

AsthmaDermatitis, AtopicGATA3 Transcription FactorHumansImmunity, InnateInflammationInterleukin-13Interleukin-4Interleukin-5Myeloid CellsTh2 CellsGATA3 protein, humanGATA3 Transcription FactorIL4 protein, humanIL5 protein, humanInterleukin-13Interleukin-4Interleukin-5allergic inflammationgroup 2 innate lymphoid cellsmyeloid cell

Identifiers

PMID32609880
PMCPMC7450169

What OpenQuestion holds

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Registered trials

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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.