Evidence map›Paper›PMID 35044462›Full record

ArticleThe Journal of experimental medicine2022

Angiotensin II enhances group 2 innate lymphoid cell responses via AT1a during airway inflammation.

Gaoyu Liu, Yingying Chen, Ying Wang, Xiaohui Deng, Qiang Xiao, Lijuan Zhang, Haixu Xu, Xu Han, Aihua Lei, Juan He and 13 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Group 2 innate lymphoid cells: Where are we 15 years out?The Journal of allergy and clinical immunology · 2026
    Review
  3. Article
  4. The immunoproteasome regulates ILC2 responses by modulating mitochondrial capacity.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  5. Antibodies to angiotensin II type 1 receptor and endothelin type A receptor are associated with cytokine production enriched for type 2 immune response and antibody production in pediatric kidney transplant recipients.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2025
    Article
  6. Article
  7. The immunology of asthma.Nature immunology · 2025
    Review
  8. Article
  9. Review
  10. Article
  11. 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

23 authors at 6 institutions in 2 countries.

Gaoyu LiuJoint Program in Immunology, Department of Internal Medicine, Affiliated Guangzhou Women and Children's Medical Center, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China.ORCID 0000-0001-8487-2815
Yingying ChenKey Laboratory of Immune Microenvironment and Disease of the Ministry of Education, Department of Immunology, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, China.ORCID 0000-0002-1669-3003
Ying WangKey Laboratory of Immune Microenvironment and Disease of the Ministry of Education, Department of Immunology, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, China.ORCID 0000-0001-6902-3217
Xiaohui DengInstitute of Human Virology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China.ORCID 0000-0003-0030-439X
Qiang XiaoDepartment of Clinical Laboratory, Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai, China.ORCID 0000-0001-8495-2882
Lijuan ZhangKey Laboratory of Immune Microenvironment and Disease of the Ministry of Education, Department of Immunology, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, China.ORCID 0000-0001-6720-6001
Haixu XuKey Laboratory of Immune Microenvironment and Disease of the Ministry of Education, Department of Immunology, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, China.ORCID 0000-0002-8310-2461
Xu HanKey Laboratory of Immune Microenvironment and Disease of the Ministry of Education, Department of Immunology, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, China.ORCID 0000-0003-1068-4517
Aihua LeiInstitute of Human Virology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China.ORCID 0000-0002-1498-5520
Juan HeJoint Program in Immunology, Department of Internal Medicine, Affiliated Guangzhou Women and Children's Medical Center, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China.ORCID 0000-0001-8568-5480
Xing LiThird Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.ORCID 0000-0001-9145-4769
Yingjiao CaoInstitute of Human Virology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China.ORCID 0000-0003-1689-0397
Pan ZhouKey Laboratory of Immune Microenvironment and Disease of the Ministry of Education, Department of Immunology, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, China.ORCID 0000-0002-7105-6808
Chunhui HeDepartment of Respiration, Guangzhou Women and Children's Medical Center, Guangzhou, China.ORCID 0000-0001-9870-242X
Peiqiong WuDepartment of Respiration, Guangzhou Women and Children's Medical Center, Guangzhou, China.ORCID 0000-0001-6492-3187
Wenhui JiangDepartment of Respiration, Guangzhou Women and Children's Medical Center, Guangzhou, China.ORCID 0000-0002-1786-3617
Meizheng TanDepartment of Child Health Care, Guangzhou Institute of Pediatrics, Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.ORCID 0000-0003-3102-0066
Chun ChenDivision of Hematology/Oncology, Department of Pediatrics, Seventh Affiliated Hospital, Sun Yat-Sen University, Shenzhen, China.ORCID 0000-0002-7103-3374
Quan YangKey Laboratory of Immunology, Sino-French Hoffmann Institute, School of Basic Medical Sciences, Guangdong Provincial Key Laboratory of Allergy and Clinical Immunology, Second Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.ORCID 0000-0002-2778-6862
Liwei LuDepartment of Pathology and Shenzhen Institute of Research and Innovation, Shenzhen Hospital, University of Hong Kong, Hong Kong, China.ORCID 0000-0002-8634-0967
Kai DengInstitute of Human Virology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China.ORCID 0000-0002-9973-8130
Zhi YaoKey Laboratory of Immune Microenvironment and Disease of the Ministry of Education, Department of Immunology, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, China.ORCID 0000-0001-8472-0731
Jie ZhouJoint Program in Immunology, Department of Internal Medicine, Affiliated Guangzhou Women and Children's Medical Center, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China.ORCID 0000-0001-5964-1599
Sun Yat-sen University · CNTianjin Medical University · CNGuangzhou Women and Children Medical Center · CNGuangzhou Medical University · CNSecond Affiliated Hospital of Guangzhou Medical University · CNUniversity of Hong Kong - Shenzhen Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Group 2 innate lymphoid cells (ILC2s) have emerged as critical mediators in driving allergic airway inflammation. Here, we identified angiotensin (Ang) II as a positive regulator of ILC2s. ILC2s expressed higher levels of the Ang II receptor AT1a, and colocalized with lung epithelial cells expressing angiotensinogen. Administration of Ang II significantly enhanced ILC2 responses both in vivo and in vitro, which were almost completely abrogated in AT1a-deficient mice. Deletion of AT1a or pharmacological inhibition of the Ang II-AT1 axis resulted in a remarkable remission of airway inflammation. The regulation of ILC2s by Ang II was cell intrinsic and dependent on interleukin (IL)-33, and was associated with marked changes in transcriptional profiling and up-regulation of ERK1/2 phosphorylation. Furthermore, higher levels of plasma Ang II correlated positively with the abundance of circulating ILC2s as well as disease severity in asthmatic patients. These observations reveal a critical role for Ang II in regulating ILC2 responses and airway inflammation.

Indexed as

Immunity, InnateAngiotensin IIAnimalsBiomarkersBronchial HyperreactivityDisease Models, AnimalDisease SusceptibilityInflammationInterleukin-33Lymphocyte SubsetsMiceMice, KnockoutReceptor, Angiotensin, Type 1Respiratory Tract DiseasesAngiotensin IIBiomarkersInterleukin-33Receptor, Angiotensin, Type 1

Identifiers

PMID35044462
PMCPMC8932533
OpenAlexW4205491447

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.