Evidence map›Paper›PMID 33589340›Full record

ArticleJournal of cystic fibrosis : official journal of the European Cystic Fibrosis Society2021

Neutrophil dysfunction in cystic fibrosis.

Lael M Yonker, Anika Marand, Sinan Muldur, Alex Hopke, Hui Min Leung, Denis De La Flor, Grace Park, Hanna Pinsky, Lauren B Guthrie, Guillermo J Tearney and 2 more

Open access · greenAbstract read
In one paragraph

Article in Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

25 citing papers in PubMed, 33 citations in OpenAlex.

  1. Phage-Based Approaches to ChronicAntibiotics (Basel, Switzerland) · 2026
    Review
  2. Review
  3. Microbial and host innate immune factors affecting the persistence ofFrontiers in cellular and infection microbiology · 2026
    Review
  4. Review
  5. Neutrophil store-operated CaJournal of cystic fibrosis : official journal of the European Cystic Fibrosis Society · 2025
    Article
  6. Article
  7. Spatial self-organization of confined bacterial suspensions.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Depths of Dysfunctional Epithelial and Immune Crosstalk in Cystic Fibrosis Revealed.American journal of respiratory and critical care medicine · 2024
    Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Super resolution microscopy analysis reveals increased Orai1 activity in asthma and cystic fibrosis lungs.Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society · 2023
    Article
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

12 authors at 3 institutions in 1 country.

Lael M YonkerMassachusetts General Hospital, Department of Pediatrics, Pulmonary Division, Boston, MA, United States; Massachusetts General Hospital, Mucosal Immunology and Biology Research Center, Boston, MA, United States; Harvard Medical School, Department of Pediatrics, Boston, MA, United States. Electronic address: lyonker@mgh.harvard.edu.
Anika MarandMassachusetts General Hospital, Center for Engineering in Medicine, Boston, MA, United States; Shriners Hospital for Children, Boston, MA, United States.
Sinan MuldurMassachusetts General Hospital, Center for Engineering in Medicine, Boston, MA, United States; Harvard Medical School, Department of Surgery, Boston, MA, United States; Shriners Hospital for Children, Boston, MA, United States.
Alex HopkeMassachusetts General Hospital, Center for Engineering in Medicine, Boston, MA, United States; Harvard Medical School, Department of Surgery, Boston, MA, United States; Shriners Hospital for Children, Boston, MA, United States.
Hui Min LeungMassachusetts General Hospital, Wellman Center for Photomedicine, Boston, MA, United States; Harvard Medical School, Department of Dermatology, Boston, MA, United States.
Denis De La FlorMassachusetts General Hospital, Mucosal Immunology and Biology Research Center, Boston, MA, United States.
Grace ParkMassachusetts General Hospital, Department of Pediatrics, Pulmonary Division, Boston, MA, United States.
Hanna PinskyMassachusetts General Hospital, Department of Pediatrics, Pulmonary Division, Boston, MA, United States.
Lauren B GuthrieMassachusetts General Hospital, Department of Pediatrics, Pulmonary Division, Boston, MA, United States.
Guillermo J TearneyMassachusetts General Hospital, Wellman Center for Photomedicine, Boston, MA, United States; Harvard Medical School, Department of Pathology, Boston, MA, United States; Harvard Medical School, Department of Dermatology, Boston, MA, United States.
Daniel IrimiaMassachusetts General Hospital, Center for Engineering in Medicine, Boston, MA, United States; Harvard Medical School, Department of Surgery, Boston, MA, United States; Shriners Hospital for Children, Boston, MA, United States.
Bryan P HurleyMassachusetts General Hospital, Mucosal Immunology and Biology Research Center, Boston, MA, United States; Harvard Medical School, Department of Pediatrics, Boston, MA, United States.
Harvard University · USMassachusetts General Hospital · USShriners Hospitals for Children - Erie · US

Funding

The Role of Hepoxilin A3 in Neutrophil Breach of the Infected Airway MucosaR01AI095338 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI HURLEY, BRYAN P · 2012 to 2022
$5.2M
Neutrophil Decision Making in Confined Environments in Health and DiseaseR01GM092804 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI IRIMIA, DANIEL · 2010 to 2022
$4.3M
Microfluidic Assessment of Clinical Outcomes in Preterm NewbornsR01HD089939 · NICHD · UNIVERSITY OF FLORIDA · PI IRIMIA, DANIEL, MOLDAWER, LYLE L · 2017 to 2021
$3.3M
Defining neutrophil pathobiology in pediatric Long COVIDR01HL173059 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI Lael Yonker · 2024 to 2026
$2.4M
Mechanistically Disentangling the Infected, Inflamed LungK08HL143183 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI YONKER, LAEL · 2018 to 2022
$869k
NHLBI NIH HHS K08 HL143183NHLBI NIH HHS R01 HL173059NIAID NIH HHS L40 AI120042NIAID NIH HHS R01 AI095338NICHD NIH HHS R01 HD089939NIGMS NIH HHS R01 GM092804
6 · The paper itself

Abstract

backgroundExcessive neutrophil inflammation is the hallmark of cystic fibrosis (CF) airway disease. Novel technologies for characterizing neutrophil dysfunction may provide insight into the nature of these abnormalities, revealing a greater mechanistic understanding and new avenues for CF therapies that target these mechanisms.

methodsBlood was collected from individuals with CF in the outpatient clinic, CF individuals hospitalized for a pulmonary exacerbation, and non-CF controls. Using microfluidic assays and advanced imaging technologies, we characterized 1) spontaneous neutrophil migration using microfluidic motility mazes, 2) neutrophil migration to and phagocytosis of Staphylococcal aureus particles in a microfluidic arena, 3) neutrophil swarming on Candida albicans clusters, and 4) Pseudomonas aeruginosa-induced neutrophil transepithelial migration using micro-optical coherence technology (µOCT).

resultsParticipants included 44 individuals: 16 Outpatient CF, 13 Hospitalized CF, and 15 Non-CF individuals. While no differences were seen with spontaneous migration, CF neutrophils migrated towards S. aureus particles more quickly than non-CF neutrophils (p < 0.05). CF neutrophils, especially Hospitalized CF neutrophils, generated significantly larger aggregates around S. aureus particles over time. Hospitalized CF neutrophils were more likely to have dysfunctional swarming (p < 0.01) and less efficient clearing of C. albicans (p < 0.0001). When comparing trans-epithelial migration towards Pseudomonas aeruginosa epithelial infection, Outpatient CF neutrophils displayed an increase in the magnitude of transmigration and adherence to the epithelium (p < 0.05).

conclusionsAdvanced technologies for characterizing CF neutrophil function reveal significantly altered migratory responses, cell-to-cell clustering, and microbe containment. Future investigations will probe mechanistic basis for abnormal responses in CF to identify potential avenues for novel anti-inflammatory therapeutics.

Indexed as

AdultCandida albicansCell MovementCystic FibrosisFemaleHumansInflammationMaleMicrofluidic Analytical TechniquesNeutrophilsPhagocytosisPseudomonas aeruginosaStaphylococcus aureusTomography, Optical CoherenceCystic fibrosisInflammationMicro-fluidicsMicro-optical coherence tomographyNeutrophil

Identifiers

PMID33589340
PMCPMC8568301
OpenAlexW3131000747

What OpenQuestion holds

Textmetadata
LicenceTDM
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.