Evidence map›Paper›PMID 31312878›Full record

ReviewCellular and molecular life sciences : CMLS2019

Cell-surface molecule-mediated cell-cell interactions in the regulation of ILC2-driven allergic inflammation.

Aihua Lei, Jie Zhou

Open access · greenAbstract readReview
In one paragraph

Review in Cellular and molecular life sciences : CMLS, 2019. 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
0.5field-weighted citation impact, top 35% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Engineering nanoparticle therapeutics for food allergy.The Journal of allergy and clinical immunology · 2024
    Review
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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

2 authors at 2 institutions in 1 country.

Aihua LeiInstitute of Pathogenic Biology, Hengyang Medical College, University of South China, Hengyang, 421001, Hunan, China.
Jie ZhouKey Laboratory of Immune Microenvironment and Disease (Ministry of Education), Department of Immunology, School of Basic Medical Sciences, Tianjin Medical University, 22 Qixiangtai Road, Tianjin, 300070, China. zhoujie@tmu.edu.cn.ORCID http://orcid.org/0000-0002-6234-033X
Tianjin Medical University · CNUniversity of South China · CN

Funding

National Natural Science Foundation of China (CN) 81571520National Natural Science Foundation of China (CN) 81742002National Natural Science Foundation of China (CN) 81771665National Natural Science Foundation of China (CN) 81800031National Natural Science Foundation of China (CN) 91542112Natural Science Foundation of Guangdong Province 2017B030311014Natural Science Foundation of Guangdong Province 2018A030313648Science and Technology Program of Guangzhou 201707010452
6 · The paper itself

Abstract

Group 2 innate lymphoid cells (ILC2s) are a subset of innate immune cells that do not express antigen receptors. ILC2-mediated type 2 responses, which are mainly characterized by the production of interleukin (IL)-5 and IL-13, play key roles in inducing inflammation, protecting against infection, and maintaining tissue homeostasis. Although recent years have largely enhanced our understanding of the transcriptional networks and soluble mediators that regulate ILC2 development or function, emerging evidence suggests that ILC2s express a variety of cell-surface molecules and interact with themselves or other immune cells. These cell-cell interactions are essential in the modulation of ILC2 number and their type 2 cytokine production during ILC2-driven allergic inflammation. In this review, we summarize the extensive array of cell-surface molecules on ILC2s that mediate cell-cell interactions and their role in regulating ILC2 generation or function in the context of ILC2-induced allergic inflammation.

Indexed as

AnimalsCell CommunicationCytokinesHumansHypersensitivityImmunity, InnateInflammationLymphocytesCytokinesAllergic inflammationCell-surface moleculesILC2

Identifiers

PMID31312878
PMCPMC11105661
OpenAlexW2960310113

What OpenQuestion holds

Textmetadata
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.