Evidence map›Paper›PMID 33400692›Full record

ArticleJCI insight2021

STING activation in alveolar macrophages and group 2 innate lymphoid cells suppresses IL-33-driven type 2 immunopathology.

Li She, Gema D Barrera, Liping Yan, Hamad H Alanazi, Edward G Brooks, Peter H Dube, Yilun Sun, Hong Zan, Daniel P Chupp, Nu Zhang and 3 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

21 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. Article
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  8. Article
  9. Group 2 innate lymphoid cells suppress neuroinflammation and brain injury following intracerebral hemorrhage.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2024
    Article
  10. Article
  11. The preprogrammed anti-inflammatory phenotypes of CD11cJournal of translational medicine · 2023
    Article
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  13. 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

13 authors at 2 institutions in 2 countries.

Li SheDepartment of Microbiology, Immunology and Molecular Genetics, Long School of Medicine, University of Texas Health San Antonio, San Antonio, Texas, USA.
Gema D BarreraDepartment of Microbiology, Immunology and Molecular Genetics, Long School of Medicine, University of Texas Health San Antonio, San Antonio, Texas, USA.
Liping YanDepartment of Microbiology, Immunology and Molecular Genetics, Long School of Medicine, University of Texas Health San Antonio, San Antonio, Texas, USA.
Hamad H AlanaziDepartment of Microbiology, Immunology and Molecular Genetics, Long School of Medicine, University of Texas Health San Antonio, San Antonio, Texas, USA.
Edward G BrooksDivision of Immunology and Infectious Disease, Long School of Medicine, University of Texas Health San Antonio, San Antonio, Texas, USA.
Peter H DubeDepartment of Microbiology, Immunology and Molecular Genetics, Long School of Medicine, University of Texas Health San Antonio, San Antonio, Texas, USA.
Yilun SunDepartment of Microbiology, Immunology and Molecular Genetics, Long School of Medicine, University of Texas Health San Antonio, San Antonio, Texas, USA.
Hong ZanDepartment of Microbiology, Immunology and Molecular Genetics, Long School of Medicine, University of Texas Health San Antonio, San Antonio, Texas, USA.
Daniel P ChuppDepartment of Microbiology, Immunology and Molecular Genetics, Long School of Medicine, University of Texas Health San Antonio, San Antonio, Texas, USA.
Nu ZhangDepartment of Microbiology, Immunology and Molecular Genetics, Long School of Medicine, University of Texas Health San Antonio, San Antonio, Texas, USA.
Xin ZhangDepartment of Otolaryngology-Head and Neck Surgery, Xiangya Hospital, Central South University, Changsha, China.
Yong LiuDepartment of Otolaryngology-Head and Neck Surgery, Xiangya Hospital, Central South University, Changsha, China.
Xiao-Dong LiDepartment of Microbiology, Immunology and Molecular Genetics, Long School of Medicine, University of Texas Health San Antonio, San Antonio, Texas, USA.
The University of Texas Health Science Center at San Antonio · USCentral South University · CN

Funding

TISSUE CULTURE---COREP30CA054174 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Robin Jean Leach · 1991 to 2026
$59.1M
Institute for Integration of Medicine & Science: A Partnership to Improve HealthUL1TR001120 · NCATS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CLARK, ROBERT A, HARGREAVES, KENNETH M · 2013 to 2017
$16.5M
NCATS NIH HHS UL1 TR001120NCI NIH HHS P30 CA054174
6 · The paper itself

Abstract

2'3'-cGAMP is known as a nonclassical second messenger and small immune modulator that possesses potent antitumor and antiviral activities via inducing the stimulator of IFN genes-mediated (STING-mediated) signaling pathway. However, its function in regulating type 2 immune responses remains unknown. Therefore, we sought to determine a role of STING activation by 2'3'-cGAMP in type 2 inflammatory reactions in multiple mouse models of eosinophilic asthma. We discovered that 2'3'-cGAMP administration strongly attenuated type 2 lung immunopathology and airway hyperreactivity induced by IL-33 and a fungal allergen, Aspergillus flavus. Mechanistically, upon the respiratory delivery, 2'3'-cGAMP was mainly internalized by alveolar macrophages, in which it activated the STING/IFN regulatory factor 3/type I IFN signaling axis to induce the production of inhibitory factors containing IFN-α, which blocked the IL-33-mediated activation of group 2 innate lymphoid (ILC2) cells in vivo. We further demonstrated that 2'3'-cGAMP directly suppressed the proliferation and function of both human and mouse ILC2 cells in vitro. Taken together, our findings suggest that STING activation by 2'3'-cGAMP in alveolar macrophages and ILC2 cells can negatively regulate type 2 immune responses, implying that the respiratory delivery of 2'3'-cGAMP might be further developed as an alternative strategy for treating type 2 immunopathologic diseases such as eosinophilic asthma.

Indexed as

AllergensAnimalsAspergillus flavusAsthmaDisease Models, AnimalEosinophiliaFemaleGuanine NucleotidesHumansImmunity, InnateInterleukin-33In Vitro TechniquesLymphocytesMacrophages, AlveolarMembrane ProteinsMice2',3'-cyclic GMPAllergensGuanine NucleotidesIL33 protein, humanIl33 protein, mouseInterleukin-33Membrane ProteinsSTING1 protein, humanSting1 protein, mouseSTING ProteinAllergyAsthmaImmunologyInflammationInnate immunity

Identifiers

PMID33400692
PMCPMC7934858
OpenAlexW3118572716

What OpenQuestion holds

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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.