Evidence map›Paper›PMID 38522826›Full record

ArticleAmerican journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons2024

Nanoparticle targeting of neutrophil glycolysis prevents lung ischemia-reperfusion injury.

Fuyi Liao, Davide Scozzi, Dequan Zhou, Mina Maksimos, Camila Diedrich, Marlene Cano, Laneshia K Tague, Zhyi Liu, Jeffrey A Haspel, Jennifer M Leonard and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Interplay between ischemia-reperfusion and metabolic reprogramming.Apoptosis : an international journal on programmed cell death · 2026
    Review
  4. Article
  5. Article
  6. Dysregulated immunometabolism in gut inflammation.Acta biochimica et biophysica Sinica · 2026
    Review
  7. Review
  8. Article
  9. Review
  10. 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

16 authors at 4 institutions in 1 country.

Fuyi LiaoDepartment of Surgery, Washington University School of Medicine, St. Louis, Missouri, USA.
Davide ScozziDepartment of Surgery, Washington University School of Medicine, St. Louis, Missouri, USA.
Dequan ZhouDepartment of Surgery, Washington University School of Medicine, St. Louis, Missouri, USA.
Mina MaksimosDepartment of Biomedical Engineering, UT Southwestern Medical Center, Dallas, Texas, USA.
Camila DiedrichDepartment of Biomedical Engineering, UT Southwestern Medical Center, Dallas, Texas, USA.
Marlene CanoDepartment of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Laneshia K TagueDepartment of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Zhyi LiuDepartment of Surgery, Washington University School of Medicine, St. Louis, Missouri, USA.
Jeffrey A HaspelDepartment of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Jennifer M LeonardDepartment of Surgery, Washington University School of Medicine, St. Louis, Missouri, USA.
Wenjun LiDepartment of Surgery, Washington University School of Medicine, St. Louis, Missouri, USA.
Alexander S KrupnickDepartment of Surgery, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Brian W WongDepartment of Surgery, Washington University School of Medicine, St. Louis, Missouri, USA.
Daniel KreiselDepartment of Surgery, Washington University School of Medicine, St. Louis, Missouri, USA.
Abdel Kareem AzabDepartment of Biomedical Engineering, UT Southwestern Medical Center, Dallas, Texas, USA. Electronic address: abdelkareem.azab@utsouthwestern.edu.
Andrew E GelmanDepartment of Surgery, Washington University School of Medicine, St. Louis, Missouri, USA. Electronic address: gelmana@wudosis.wustl.edu.
Washington University in St. Louis · USSouthwestern Medical CenterSouthwestern Medical Center · USUniversity of Maryland, Baltimore · US

Funding

The Role of Neutrophils in Regulating Lung Transplant ToleranceP01AI116501 · NIAID · WASHINGTON UNIVERSITY · PI Andrew Eric Gelman · 2015 to 2026
$19.4M
THE ROLE OF ISCHEMIA REPERFUSION INJURY IN LUNG ALLOGRAFT REJECTIONR01HL094601 · NHLBI · WASHINGTON UNIVERSITY · PI Andrew Eric Gelman, Daniel Kreisel · 2009 to 2026
$6.9M
The Role of Eosinophils in the Lung AllograftR01AI145108 · NIAID · UNIVERSITY OF VIRGINIA · PI Elizabeth A Jacobsen, ALEXANDER S. KRUPNICK · 2019 to 2026
$4.1M
Targeting a Defined Surgical Stress-Induced Inflammatory Pathway to Improve Peri-Operative OutcomesR01HL166402 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI Elizabeth A Jacobsen, ALEXANDER S. KRUPNICK · 2023 to 2026
$2.2M
Netosis in Trauma Mediated Acute Lung InjuryK08GM137323 · NIGMS · WASHINGTON UNIVERSITY · PI LEONARD, JENNIFER · 2021 to 2024
$721k
Influence of Mycophenolic Acid Pharmacogenomics on Lung Transplant OutcomesK01HL155231 · NHLBI · WASHINGTON UNIVERSITY · PI TAGUE, LANESHIA K · 2021 to 2024
$596k
Mechanisms of Immunosurveillance for Lung Cancer-the Role of CD8+ T Cells in Tumor Tolerance InductionI01BX002299 · VA · ST. LOUIS VA MEDICAL CENTER · PI ALEXANDER S. KRUPNICK · 2014 to 2026
–
BLRD VA I01 BX002299NHLBI NIH HHS K01 HL155231NHLBI NIH HHS L70 HL165646NHLBI NIH HHS R01 HL094601NHLBI NIH HHS R01 HL166402NIAID NIH HHS P01 AI116501NIAID NIH HHS R01 AI145108NIGMS NIH HHS K08 GM137323
6 · The paper itself

Abstract

Neutrophils exacerbate pulmonary ischemia-reperfusion injury (IRI) resulting in poor short and long-term outcomes for lung transplant recipients. Glycolysis powers neutrophil activation, but it remains unclear if neutrophil-specific targeting of this pathway will inhibit IRI. Lipid nanoparticles containing the glycolysis flux inhibitor 2-deoxyglucose (2-DG) were conjugated to neutrophil-specific Ly6G antibodies (NP-Ly6G[2-DG]). Intravenously administered NP-Ly6G(2-DG) to mice exhibited high specificity for circulating neutrophils. NP-Ly6G(2-DG)-treated neutrophils were unable to adapt to hypoglycemic conditions of the lung airspace environment as evident by the loss of demand-induced glycolysis, reductions in glycogen and ATP content, and an increased vulnerability to apoptosis. NP-Ly6G(2-DG) treatment inhibited pulmonary IRI following hilar occlusion and orthotopic lung transplantation. IRI protection was associated with less airspace neutrophil extracellular trap generation, reduced intragraft neutrophilia, and enhanced alveolar macrophage efferocytotic clearance of neutrophils. Collectively, our data show that pharmacologically targeting glycolysis in neutrophils inhibits their activation and survival leading to reduced pulmonary IRI.

Indexed as

GlycolysisLung TransplantationMice, Inbred C57BLNanoparticlesNeutrophilsReperfusion InjuryAnimalsApoptosisDeoxyglucoseLungMaleMiceDeoxyglucoseacute lung injury and immunosuppressionefferocytosisglycolysisimmunometabolismischemia-reperfusion injurylung transplantnanoparticlesneutrophilsprimary graft dysfunction

Identifiers

PMID38522826
PMCPMC11305958
OpenAlexW4393129460

What OpenQuestion holds

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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.