Evidence map›Paper›PMID 40368637›Full record

ArticleACS nano2025

Nanodiamonds Interact with Primary Human Macrophages and Dendritic Cells Evoking a Vigorous Interferon Response.

Tomas Malina, Jasreen Kaur, Sebastin Martin, Audrey Gallud, Shintaro Katayama, Arianna Gazzi, Marco Orecchioni, Martin Petr, Martin Šrejber, Lars Haag and 5 more

Abstract read
In one paragraph

Article in ACS nano, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

15 authors.

Tomas MalinaInstitute of Environmental Medicine, Division of Molecular Toxicology, Karolinska Institutet, 171 77 Stockholm, Sweden.
Jasreen KaurInstitute of Environmental Medicine, Division of Molecular Toxicology, Karolinska Institutet, 171 77 Stockholm, Sweden.
Sebastin MartinInstitute of Environmental Medicine, Division of Molecular Toxicology, Karolinska Institutet, 171 77 Stockholm, Sweden.
Audrey GalludInstitute of Environmental Medicine, Division of Molecular Toxicology, Karolinska Institutet, 171 77 Stockholm, Sweden.ORCID 0000-0003-0283-4028
Shintaro KatayamaDepartment of Biosciences and Nutrition, Karolinska Institutet, 148 13 Huddinge, Sweden.ORCID 0000-0001-7581-5157
Arianna GazziDepartment of Biomedical Sciences, University of Padua, Padua 351 29, Italy.
Marco OrecchioniLa Jolla Institute for Immunology, San Diego, California 92037, United States.
Martin PetrRegional Centre of Advanced Technologies and Materials, Czech Advanced Technology and Research Institute (CATRIN), Palacký University, 772 00 Olomouc, Czech Republic.
Martin ŠrejberRegional Centre of Advanced Technologies and Materials, Czech Advanced Technology and Research Institute (CATRIN), Palacký University, 772 00 Olomouc, Czech Republic.ORCID 0000-0001-9556-2978
Lars HaagDepartment of Laboratory Medicine, Karolinska Institutet, 141 52 Huddinge, Sweden.
Bejan HamawandiDepartment of Applied Physics, KTH-Royal Institute of Technology, 106 91 Stockholm, Sweden.
Muhammet S ToprakDepartment of Applied Physics, KTH-Royal Institute of Technology, 106 91 Stockholm, Sweden.ORCID 0000-0001-5678-5298
Juha KereDepartment of Biosciences and Nutrition, Karolinska Institutet, 148 13 Huddinge, Sweden.
Lucia Gemma DeloguDepartment of Biomedical Sciences, University of Padua, Padua 351 29, Italy.
Bengt FadeelInstitute of Environmental Medicine, Division of Molecular Toxicology, Karolinska Institutet, 171 77 Stockholm, Sweden.ORCID 0000-0001-5559-8482

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nanodiamonds (NDs) display several attractive features rendering them useful for medical applications such as drug delivery. However, the interactions between NDs and the immune system remain poorly understood. Here, we investigated amino-, carboxyl-, and poly(ethylene glycol) (PEG)-terminated NDs with respect to primary human immune cells. We applied cytometry by time-of-flight (CyToF) to assess the impact on peripheral blood mononuclear cells at the single-cell level, and observed an expansion of plasmacytoid dendritic cells (pDCs) which are critically involved in antiviral responses. Subsequent experiments demonstrated that the NDs were actively internalized, leading to a vigorous type I interferon response involving endosomal Toll-like receptors. ND-NH

Indexed as

Dendritic CellsInterferon Type IMacrophagesNanodiamondsAnimalsEndosomesHumansLysosomesMicePolyethylene GlycolsRAW 264.7 CellsTHP-1 CellsToll-Like ReceptorsInterferon Type INanodiamondsPolyethylene GlycolsToll-Like Receptorsautophagydendritic cellsinterferonmacrophagesnanodiamonds

Identifiers

PMID40368637
PMCPMC12120995

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.