Evidence map›Paper›PMID 30894497›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

Development of highly potent glucocorticoids for steroid-resistant severe asthma.

Yuanzheng He, Jingjing Shi, Quang Tam Nguyen, Erli You, Hongbo Liu, Xin Ren, Zhongshan Wu, Jianshuang Li, Wenli Qiu, Sok Kean Khoo and 8 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Article
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  4. Article
  5. Article
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  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Structural insights into glucocorticoid receptor function.Biochemical Society transactions · 2021
    Review
  13. Cutting Edge: Steroid Responsiveness in Foxp3Journal of immunology (Baltimore, Md. : 1950) · 2021
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. 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

18 authors.

Yuanzheng HeLaboratory of Receptor Structure and Signaling, HIT Center for Life Science, Harbin Institute of Technology, Harbin 150001, China; ajian.he@hit.edu.cn yiwei@gzhmu.edu.cn minb@ccf.org eric.xu@vai.org.
Jingjing ShiVan Andel Research Institute-Shanghai Institute of Materia Medica, Center for Structure and Function of Drug Targets, Key Laboratory of Receptor Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China.
Quang Tam NguyenDepartment of Inflammation and Immunity, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, OH 44195.
Erli YouVan Andel Research Institute-Shanghai Institute of Materia Medica, Center for Structure and Function of Drug Targets, Key Laboratory of Receptor Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China.
Hongbo LiuCenter of Epigenetics, Van Andel Research Institute, Grand Rapids, MI 49503.
Xin RenDepartment of Medicine, Lung Biology Center, University of California, San Francisco, CA 94158.
Zhongshan WuDepartment of Research and Development, Palo Alto Pharmaceuticals, Shanghai 201203, China.
Jianshuang LiLaboratory of Skeletal Biology, Van Andel Research Institute, Grand Rapids, MI 49503.
Wenli QiuDepartment of Medicine, Lung Biology Center, University of California, San Francisco, CA 94158.
Sok Kean KhooDepartment of Cell and Molecular Biology, Grand Valley State University, Grand Rapids, MI 49401.
Tao YangLaboratory of Skeletal Biology, Van Andel Research Institute, Grand Rapids, MI 49503.
Wei YiVan Andel Research Institute-Shanghai Institute of Materia Medica, Center for Structure and Function of Drug Targets, Key Laboratory of Receptor Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China; ajian.he@hit.edu.cn yiwei@gzhmu.edu.cn minb@ccf.org eric.xu@vai.org.
Feng SunDepartment of Research and Development, Palo Alto Pharmaceuticals, Shanghai 201203, China.
Zhijian XiDepartment of Research and Development, Palo Alto Pharmaceuticals, Shanghai 201203, China.
Xiaozhu HuangDepartment of Medicine, Lung Biology Center, University of California, San Francisco, CA 94158.
Karsten MelcherLaboratory of Structural Sciences, Van Andel Research Institute, Grand Rapids, MI 49503.ORCID 0000-0002-9125-4027
Booki MinDepartment of Inflammation and Immunity, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, OH 44195; ajian.he@hit.edu.cn yiwei@gzhmu.edu.cn minb@ccf.org eric.xu@vai.org.
H Eric XuLaboratory of Structural Sciences, Van Andel Research Institute, Grand Rapids, MI 49503; ajian.he@hit.edu.cn yiwei@gzhmu.edu.cn minb@ccf.org eric.xu@vai.org.

Funding

The role of IL-27/Lag3 axis in regulating Foxp3+ regulatory T cell functionR01AI125247 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Booki Min · 2017 to 2026
$3.4M
Preclinical Study of IL-27-Conditioned Tregs to Treat GvHDR21AI121524 · NIAID · CLEVELAND CLINIC LERNER COM-CWRU · PI HAMILTON, BETTY K, MIN, BOOKI · 2016 to 2017
$436k
NIAID NIH HHS R01 AI125247NIAID NIH HHS R21 AI121524
6 · The paper itself

Abstract

Clinical application of inhaled glucocorticoids (GCs) has been hampered in the case of steroid-resistant severe asthma. To overcome this limitation, we have developed a series of highly potent GCs, including VSGC12, VSG158, and VSG159 based on the structural insight into the glucocorticoid receptor (GR). Particularly, VSG158 exhibits a maximal repression of lung inflammation and is 10 times more potent than the currently most potent clinical GC, Fluticasone Furoate (FF), in a murine model of asthma. More importantly, VSG158 displays a unique property to reduce neutrophilic inflammation in a steroid-resistant airway inflammation model, which is refractory to clinically available GCs, including dexamethasone and FF. VSG158 and VSG159 are able to deliver effective treatments with reduced off-target and side effects. In addition, these GCs also display pharmacokinetic properties that are suitable for the inhalation delivery method for asthma treatment. Taken together, the excellent therapeutic and side-effect profile of these highly potent GCs holds promise for treating steroid-resistant severe asthma.

Indexed as

Anti-Asthmatic AgentsDrug DevelopmentGlucocorticoidsAnimalsAsthmaDisease Models, AnimalFemaleMaleMiceReceptors, GlucocorticoidSeverity of Illness IndexAnti-Asthmatic AgentsGlucocorticoidsReceptors, Glucocorticoidglucocorticoidhigh potencysteroid-resistant asthmaVSG158VSG159

Identifiers

PMID30894497
PMCPMC6452690

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.