Evidence map›Paper›PMID 30464452›Full record

ArticleInternational journal of nanomedicine2018

Functionalization-dependent effects of cellulose nanofibrils on tolerogenic mechanisms of human dendritic cells.

Sergej Tomić, Nataša Ilić, Vanja Kokol, Alisa Gruden-Movsesijan, Dušan Mihajlović, Marina Bekić, Ljiljana Sofronić-Milosavljević, Miodrag Čolić, Dragana Vučević

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. 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

9 authors.

Sergej TomićInstitute for the Application of Nuclear Energy, University of Belgrade, Belgrade, Serbia, sergej.tomic@inep.co.rs.
Nataša IlićInstitute for the Application of Nuclear Energy, University of Belgrade, Belgrade, Serbia, sergej.tomic@inep.co.rs.
Vanja KokolInstitute of Engineering Materials and Design, University of Maribor, Maribor, Slovenia.
Alisa Gruden-MovsesijanInstitute for the Application of Nuclear Energy, University of Belgrade, Belgrade, Serbia, sergej.tomic@inep.co.rs.
Dušan MihajlovićInstitute for Medical Research, Medical Faculty of the Military Medical Academy, University of Defense, Belgrade, Serbia, sergej.tomic@inep.co.rs.
Marina BekićInstitute for the Application of Nuclear Energy, University of Belgrade, Belgrade, Serbia, sergej.tomic@inep.co.rs.
Ljiljana Sofronić-MilosavljevićInstitute for the Application of Nuclear Energy, University of Belgrade, Belgrade, Serbia, sergej.tomic@inep.co.rs.
Miodrag ČolićInstitute for the Application of Nuclear Energy, University of Belgrade, Belgrade, Serbia, sergej.tomic@inep.co.rs.
Dragana VučevićInstitute for Medical Research, Medical Faculty of the Military Medical Academy, University of Defense, Belgrade, Serbia, sergej.tomic@inep.co.rs.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCellulose nanofibrils (CNF) are attractive nanomaterials for various biomedical applications due to their excellent biocompatibility and biomimetic properties. However, their immunoregulatory properties are insufficiently investigated, especially in relation to their functionalization, which could cause problems during their clinical application.

methodsUsing a model of human dendritic cells (DC), which have a central role in the regulation of immune response, we investigated how differentially functionalized CNF, ie, native (n) CNF, 2,2,6,6-tetramethylpiperidine 1-oxyl radical-oxidized (c) CNF, and 3-aminopropylphosphoric acid-functionalized (APAc) CNF, affect DC properties, their viability, morphology, differentiation and maturation potential, and the capacity to regulate T cell-mediated immune response.

resultsNontoxic doses of APAcCNF displayed the strongest inhibitory effects on DC differentiation, maturation, and T helper (Th) 1 and Th17 polarization capacity, followed by cCNF and nCNF, respectively. These results correlated with a specific pattern of regulatory cytokines production by APAcCNF-DC and their increased capacity to induce suppressive CD8

conclusionThe capacity to induce different types of DC-mediated tolerogenic immune responses by functionalized CNF opens new perspectives for their application as well-tolerated nanomaterials in tissue engineering and novel platforms for the therapy of inflammatory T cell-mediated pathologies.

Indexed as

Immune ToleranceCell DifferentiationCell PolarityCell ProliferationCell SurvivalCelluloseCytokinesDendritic CellsHumansIndoleamine-Pyrrole 2,3,-DioxygenaseNanofibersPhenotypePiperidinesTh17 CellsTh1 CellsT-Lymphocytes, Regulatory2,2,6,6-tetramethylpiperidideCelluloseCytokinesIDO1 protein, humanIndoleamine-Pyrrole 2,3,-DioxygenasePiperidinesbiocompatibilitycellulose nanofibrilsimmunomodulationregulatory T-cell subsetstolerogenic dendritic cells

Identifiers

PMID30464452
PMCPMC6217907

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.