Evidence map›Paper›PMID 36674876›Full record

ArticleInternational journal of molecular sciences2023

Effects of Magnetic Nanoparticles on the Functional Activity of Human Monocytes and Dendritic Cells.

Marta Donini, Francesca Pettinella, Giorgia Zanella, Salvatore Calogero Gaglio, Carlo Laudanna, Monica Jimenez-Carretero, Concepcion Jimenez-Lopez, Massimiliano Perduca, Stefano Dusi

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
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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

9 authors at 2 institutions in 2 countries.

Marta DoniniSection of General Pathology, Department of Medicine, University of Verona, Strada Le Grazie 8, 37134 Verona, Italy.
Francesca PettinellaSection of General Pathology, Department of Medicine, University of Verona, Strada Le Grazie 8, 37134 Verona, Italy.
Giorgia ZanellaDepartment of Biotechnology, University of Verona, Strada Le Grazie 15, 37134 Verona, Italy.
Salvatore Calogero GaglioDepartment of Biotechnology, University of Verona, Strada Le Grazie 15, 37134 Verona, Italy.
Carlo LaudannaSection of General Pathology, Department of Medicine, University of Verona, Strada Le Grazie 8, 37134 Verona, Italy.ORCID 0000-0003-4050-1056
Monica Jimenez-CarreteroDepartment of Microbiology, Faculty of Sciences, University of Granada, 18071 Granada, Spain.ORCID 0000-0002-5867-2083
Concepcion Jimenez-LopezDepartment of Microbiology, Faculty of Sciences, University of Granada, 18071 Granada, Spain.ORCID 0000-0002-5645-2079
Massimiliano PerducaDepartment of Biotechnology, University of Verona, Strada Le Grazie 15, 37134 Verona, Italy.ORCID 0000-0001-8291-0523
Stefano DusiSection of General Pathology, Department of Medicine, University of Verona, Strada Le Grazie 8, 37134 Verona, Italy.ORCID 0000-0001-9753-5076
University of Verona · ITUniversidad de Granada · ES

Funding

FEDER Operational Program B-BIO-432-UGR20Instituto de Salud Carlos III PI20-01658Ministry of Economy, Industry and Competitiveness PDC2021-121135.100University of Verona FUR (Fondo Unico della Ricerca)
6 · The paper itself

Abstract

The use of nanoparticles in medicine is sometimes hampered by their potential to activate immune cells, eliciting inflammation or allergy. We investigated whether magnetic nanoparticles (MNPs) or biomimetic magnetic nanoparticles (BMNPs) affect relevant activities of human monocytes. We found that the nanoparticles neither elicited the production of pro-inflammatory mediators IL-6 and TNFα by resting monocytes (when BMNP dose < 300 μg/mL) nor enhanced their secretion induced by R848, a molecule engaging virus-recognizing receptors, or bacterial lipopolysaccharide (LPS). MNPs and BMNPs neither induced the generation of reactive oxygen species (ROS), nor affected the ROS production elicited by the NADPH oxidase activator phorbol myristate acetate (PMA) or the fungal derivative β-glucan. BMNPs, but not MNPs, caused an up-regulation of the maturation markers CD80, CD83, and CD86 in immature monocyte-derived dendritic cells (DCs), whereas both nanoparticles did not affect the LPS-induced expression of these markers. Moreover, the nanoparticles were greedily ingested by monocytes and DCs without altering their viability. Therefore, these nanoparticles are candidates for medical applications because they do not activate pro-inflammatory activities of monocytes. Furthermore, their ability to stimulate DC maturation could be used for the design of vaccines. Moreover, harmlessly engulfed nanoparticles could be vehicles to carry molecules inside the immune cells to regulate the immune response.

Indexed as

Magnetite NanoparticlesMonocytesCell DifferentiationCells, CulturedCytokinesDendritic CellsHumansLipopolysaccharidesReactive Oxygen SpeciesCytokinesLipopolysaccharidesMagnetite NanoparticlesReactive Oxygen Speciesdendritic cellsimmunityinflammationmagnetic nanoparticlesmonocytespro-inflammatory mediatorsreactive oxygen species

Identifiers

PMID36674876
PMCPMC9864373
OpenAlexW4315649532

What OpenQuestion holds

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LicenceCC BY
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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.