Evidence map›Paper›PMID 32659786›Full record

Trial reportBlood2020

Glucocorticoid-induced eosinopenia results from CXCR4-dependent bone marrow migration.

So Gun Hong, Noriko Sato, Fanny Legrand, Manasi Gadkari, Michelle Makiya, Kindra Stokes, Katherine N Howe, Shiqin Judy Yu, Nathaniel Seth Linde, Randall R Clevenger and 6 more

Registry-linked trialOpen access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Blood, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02798523 (Genomic Response of Human Immune and Non-Immune Cells to Glucocorticoids), which is not on this map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.9field-weighted citation impact, top 5% 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.

NCT02798523 phase1completednot on this map

Genomic Response of Human Immune and Non-Immune Cells to Glucocorticoids

TypeinterventionalSponsorNational Institute of Allergy and Infectious Diseases (NIAID)Ran2017 to 2022Enrolled33ConditionsNormal PhysiologyArmsMethylprednisolone sodium succinate(Solu-Medrol), Topical methylprednisolone (Advantan emulsion 0 /1%)
3 · Its place in the literature

Who cites it

30 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Social Housing of Postoperative Animals to Support Animal Welfare.Journal of the American Association for Laboratory Animal Science : JAALAS · 2026
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. In vivo tracking of ex-vivo-generatedMolecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  16. Non-Malignant Granulocyte and Monocyte Disorders: An Update.British journal of biomedical science · 2025
    Review
  17. Article
  18. Article
  19. Immune Response Dynamics and Biomarkers in COVID-19 Patients.International journal of molecular sciences · 2024
    Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 4 institutions in 2 countries.

So Gun HongTranslational Stem Cell Biology Branch, National Heart, Lung, and Blood Institute.
Noriko SatoMolecular Imaging Program, National Cancer Institute.
Fanny LegrandHuman Eosinophil Section, Laboratory of Parasitic Diseases.
Manasi GadkariLaboratory of Immune System Biology, and.
Michelle MakiyaHuman Eosinophil Section, Laboratory of Parasitic Diseases.
Kindra StokesHuman Eosinophil Section, Laboratory of Parasitic Diseases.
Katherine N HoweLaboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases.
Shiqin Judy YuTranslational Stem Cell Biology Branch, National Heart, Lung, and Blood Institute.
Nathaniel Seth LindeTranslational Stem Cell Biology Branch, National Heart, Lung, and Blood Institute.
Randall R ClevengerAnimal Surgery and Resources Core, National Heart, Lung, and Blood Institute, and.
Timothy HuntAnimal Surgery and Resources Core, National Heart, Lung, and Blood Institute, and.
Zonghui HuBiostatistics Research Branch, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD.
Peter L ChoykeMolecular Imaging Program, National Cancer Institute.
Cynthia E DunbarTranslational Stem Cell Biology Branch, National Heart, Lung, and Blood Institute.
Amy D KlionHuman Eosinophil Section, Laboratory of Parasitic Diseases.
Luis M FrancoLaboratory of Immune System Biology, and.
National Heart Lung and Blood Institute · USMorphoSys (Germany) · DENational Institute of Allergy and Infectious Diseases · USNational Institutes of Health · US

Funding

Retroviral Mediated Gene Transfer Into Primate Hematopoietic CellsZIAHL002338 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI HONG, SO GUN · 2019 to 2025
$26.3M
Understanding hematopoietic stem cell mobilization and engraftmentZIAHL006063 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI DUNBAR, CYNTHIA E · 2010 to 2025
$23.5M
Eosinophils and Eosinophil Activation in the Pathogenesis of Human DiseaseZIAAI001130 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI KLION, AMY · 2010 to 2025
$22.5M
Integrative genomic analysis of the human response to glucocorticoidsZIAAR041213 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI FRANCO, LUIS · 2020 to 2025
$4.8M
6 · The paper itself

Abstract

Glucocorticoids are considered first-line therapy in a variety of eosinophilic disorders. They lead to a transient, profound decrease in circulating human eosinophils within hours of administration. The phenomenon of glucocorticoid-induced eosinopenia has been the basis for the use of glucocorticoids in eosinophilic disorders, and it has intrigued clinicians for 7 decades, yet its mechanism remains unexplained. To investigate, we first studied the response of circulating eosinophils to in vivo glucocorticoid administration in 3 species and found that the response in rhesus macaques, but not in mice, closely resembled that in humans. We then developed an isolation technique to purify rhesus macaque eosinophils from peripheral blood and performed live tracking of zirconium-89-oxine-labeled eosinophils by serial positron emission tomography/computed tomography imaging, before and after administration of glucocorticoids. Glucocorticoids induced rapid bone marrow homing of eosinophils. The kinetics of glucocorticoid-induced eosinopenia and bone marrow migration were consistent with those of the induction of the glucocorticoid-responsive chemokine receptor CXCR4, and selective blockade of CXCR4 reduced or eliminated the early glucocorticoid-induced reduction in blood eosinophils. Our results indicate that glucocorticoid-induced eosinopenia results from CXCR4-dependent migration of eosinophils to the bone marrow. These findings provide insight into the mechanism of action of glucocorticoids in eosinophilic disorders, with implications for the study of glucocorticoid resistance and the development of more targeted therapies. The human study was registered at ClinicalTrials.gov as #NCT02798523.

Indexed as

AnimalsBone MarrowEosinophilsFemaleGlucocorticoidsHumansLeukopeniaMacaca mulattaMaleMiceReceptors, CXCR4CXCR4 protein, humanCXCR4 protein, mouseGlucocorticoidsReceptors, CXCR4

Identifiers

PMID32659786
PMCPMC7735160
OpenAlexW3043642888

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.