Evidence map›Paper›PMID 33178840›Full record

ArticleJournal of immunology research2020

Tissue-Resident Type 2 Innate Lymphoid Cells Arrest Alveolarization in Bronchopulmonary Dysplasia.

Lanlan Mi, Shaoxuan Zhu, Jiayu Cai, Suqing Xu, Zhengyang Xue, Hongyan Lu

Open access · goldAbstract read
In one paragraph

Article in Journal of immunology research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 30% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. [Changes and significance of type 2 innate lymphoid cells and their related factors in bronchopulmonary dysplasia].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2023
    Article
  7. The Role of the Interleukin-1 Family in Complications of Prematurity.International journal of molecular sciences · 2023
    Review
  8. Article
  9. Crosstalk between ILC2s and Th2 CD4Journal of immunology research · 2022
    Review
  10. 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

6 authors at 1 institution in 1 country.

Lanlan MiDepartment of Pediatrics, The Affiliated Hospital of Jiangsu University, Zhenjiang 212001, China.ORCID https://orcid.org/0000-0002-3541-5551
Shaoxuan ZhuDepartment of Pediatrics, The Affiliated Hospital of Jiangsu University, Zhenjiang 212001, China.ORCID https://orcid.org/0000-0001-5378-5479
Jiayu CaiDepartment of Pediatrics, The Affiliated Hospital of Jiangsu University, Zhenjiang 212001, China.ORCID https://orcid.org/0000-0001-5303-7876
Suqing XuDepartment of Pediatrics, The Affiliated Hospital of Jiangsu University, Zhenjiang 212001, China.ORCID https://orcid.org/0000-0003-0534-4825
Zhengyang XueDepartment of Pediatrics, The Affiliated Hospital of Jiangsu University, Zhenjiang 212001, China.ORCID https://orcid.org/0000-0002-4378-1471
Hongyan LuDepartment of Pediatrics, The Affiliated Hospital of Jiangsu University, Zhenjiang 212001, China.ORCID https://orcid.org/0000-0003-4367-2715
Jiangsu University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bronchopulmonary dysplasia (BPD) is a severe complication of the respiratory system associated with preterm birth. Type 2 innate lymphoid cells (ILC2s) play a major role in tissue homeostasis, inflammation, and wound healing. However, the role in BPD remains unclear. The present study showed that ILC2s, interleukin-4 (IL-4), IL-13, and anti-inflammatory (M2) macrophages increased significantly in BPD mice as compared to the control mice. Administration with recombinant mouse IL-33 amplified the above phenomena and aggravated the alveolar structural disorder and functional injury in mice subjected to BPD, and the opposite was true with anti-ST2 antibody. In addition, the depletion of ILC2s in BPD mice with anti-CD90.2 antibody substantially abolished the destructive effect on BPD. In the treatment of BPD with dexamethasone, the number of ILC2s and M2 macrophages and levels of IL-4 and IL-13 decreased with remission as compared to the control group. This study identified a major destructive role of the ILC2s in BPD that could be attenuated as a therapeutic strategy.

Indexed as

Immunity, InnateAnimalsBiomarkersBronchopulmonary DysplasiaCytokinesDexamethasoneDisease Models, AnimalDisease SusceptibilityFemaleImmunophenotypingLymphocytesMacrophagesMicePulmonary AlveoliBiomarkersCytokinesDexamethasone

Identifiers

PMID33178840
PMCPMC7648679
OpenAlexW3094711557

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.