Evidence map›Paper›PMID 39543655›Full record

ArticleJournal of nanobiotechnology2024

Magnetic nanoradiotracers for targeted neutrophil detection in pulmonary arterial hypertension.

Lucía Fadón-Padilla, Claudia Miranda-Pérez de Alejo, Ana Beatriz Miguel-Coello, Marta Beraza, Desiré Di Silvio, Ainhize Urkola-Arsuaga, María Jesús Sánchez-Guisado, Irati Aiestaran-Zelaia, Laura Fernández-Méndez, Lydia Martinez-Parra and 4 more

Abstract read
In one paragraph

Article in Journal of nanobiotechnology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. 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

14 authors.

Lucía Fadón-PadillaDepartment of Diagnostic Radiology and Nuclear Medicine, University of Maryland School of Medicine, Baltimore, 21201, USA.
Claudia Miranda-Pérez de AlejoCenter for Cooperative Research in Biomaterials (CIC biomaGUNE), Basque Research and Technology Alliance (BRTA), Donostia, 20014, Spain.
Ana Beatriz Miguel-CoelloCenter for Cooperative Research in Biomaterials (CIC biomaGUNE), Basque Research and Technology Alliance (BRTA), Donostia, 20014, Spain.
Marta BerazaCenter for Cooperative Research in Biomaterials (CIC biomaGUNE), Basque Research and Technology Alliance (BRTA), Donostia, 20014, Spain.
Desiré Di SilvioCenter for Cooperative Research in Biomaterials (CIC biomaGUNE), Basque Research and Technology Alliance (BRTA), Donostia, 20014, Spain.
Ainhize Urkola-ArsuagaCenter for Cooperative Research in Biomaterials (CIC biomaGUNE), Basque Research and Technology Alliance (BRTA), Donostia, 20014, Spain.
María Jesús Sánchez-GuisadoCenter for Cooperative Research in Biomaterials (CIC biomaGUNE), Basque Research and Technology Alliance (BRTA), Donostia, 20014, Spain.
Irati Aiestaran-ZelaiaCenter for Cooperative Research in Biomaterials (CIC biomaGUNE), Basque Research and Technology Alliance (BRTA), Donostia, 20014, Spain.
Laura Fernández-MéndezCenter for Cooperative Research in Biomaterials (CIC biomaGUNE), Basque Research and Technology Alliance (BRTA), Donostia, 20014, Spain.
Lydia Martinez-ParraCenter for Cooperative Research in Biomaterials (CIC biomaGUNE), Basque Research and Technology Alliance (BRTA), Donostia, 20014, Spain.
Ermal IsmalajCenter for Cooperative Research in Biomaterials (CIC biomaGUNE), Basque Research and Technology Alliance (BRTA), Donostia, 20014, Spain.
Edurne BerraCenter for Cooperative Research in Bioscience (CIC bioGUNE), Basque Research and Technology Alliance (BRTA), Derio, 4810, Spain.
Susana Carregal-RomeroCenter for Cooperative Research in Biomaterials (CIC biomaGUNE), Basque Research and Technology Alliance (BRTA), Donostia, 20014, Spain. scarregal@cicbiomagune.es.
Jesús Ruíz-CabelloCenter for Cooperative Research in Biomaterials (CIC biomaGUNE), Basque Research and Technology Alliance (BRTA), Donostia, 20014, Spain. jruizcabello@cicbiomagune.es.

Funding

Eusko Jaurlaritza 2022333041Fundación Ramon Areces CIVP21S13151Ministerio de Ciencia e Innovación CNS2023-143944, RYC2020-030241-I, PID2022-142842OB-I00Ministerio de Ciencia e Innovación PID2021-123238OB-I00
6 · The paper itself

Abstract

backgroundPulmonary arterial hypertension (PAH) is a severe disease characterized by elevated blood pressure in the pulmonary artery that can ultimately damage the right ventricle of the heart. PAH is pathophysiologically heterogeneous, which makes early diagnosis and treatment difficult. Inflammation is thought to be an important factor in the development and progression of this disease and may explain some of the observed interindividual differences. In the context of both acute and chronic inflammation, neutrophil recruitment to the lung has been suggested as a potential biomarker for studying PAH progression. However, there are currently no specific probes for its non-invasive in vivo detection. The imaging-based gold standard for assessing inflammation is [

methodsThis study investigated the potential of magnetic nanoradiotracers based on ultrasmall iron oxide nanoparticles, functionalized with N-cinnamoyl-F-(D)L-F-(D)L-F peptide, to detect increased neutrophil infiltration in vivo in different PAH animal models via positron emission tomography. These nanoprobes target formyl peptide receptor 1, which is abundantly expressed in the cell membrane of neutrophils. To assess the benefit of these nanoprobes, their biodistribution was first assessed via magnetic resonance imaging and histology. Then, their lung uptake was compared by positron emission tomography with that of

resultsOur targeted magnetic nanoradiotracer detected an increase in pulmonary neutrophil infiltration in both PAH models and distinguished between them, which was not possible with

conclusionsThis study underscores the importance of targeted imaging in providing an individualized and longitudinal evaluation of heterogeneous and multifactorial diseases such as PAH. The use of targeted multimodal nanoprobes, for magnetic resonance/positron emission tomography imaging has the potential to facilitate the diagnosis and monitoring of diseases, as well as the development of novel therapies.

Indexed as

LungNeutrophilsPulmonary Arterial HypertensionAnimalsDisease Models, AnimalFluorodeoxyglucose F18HumansHypertension, PulmonaryMagnetic Iron Oxide NanoparticlesMalePositron-Emission TomographyRadiopharmaceuticalsRatsRats, Sprague-DawleyTissue DistributionFluorodeoxyglucose F18RadiopharmaceuticalsMagnetic nanoparticlesMagnetic resonance imagingNeutrophil detectionPositron emission tomographyPulmonary arterial hypertensionTargeted molecular imaging

Identifiers

PMID39543655
PMCPMC11562838

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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.