Evidence map›Paper›PMID 38091227›Full record

ArticleImmunologic research2024

An epicutaneous therapeutic pollen-allergen extract delivery system in an allergic rhinitis mouse model: based on allergen loading on DC-specific aptamers conjugated nanogolds.

Safoora Pordel, Navideh Haghnavaz, MohammadAli Rezaee, Saeideh Sadat Shobeiri, Bahareh Ansari, Mohammadreza Dashti, Malihe Moghadam, Motahare Khorrami, Mojtaba Sankian

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Article in Immunologic research, 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
1.2field-weighted citation impact, top 19% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
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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 1 institution in 1 country.

Safoora PordelImmunology Research Center, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Navideh HaghnavazImmunology Research Center, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
MohammadAli RezaeeImmunology Research Center, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Saeideh Sadat ShobeiriImmunology Research Center, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Bahareh AnsariImmunology Research Center, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Mohammadreza DashtiImmunology Research Center, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Malihe MoghadamImmunology Research Center, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Motahare KhorramiImmunology Research Center, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Mojtaba SankianImmunology Research Center, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran. sankianm@mums.ac.ir.ORCID 0000-0003-0602-6431
Mashhad University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGold nanoparticles (GNPs) have previously been suggested as appropriate carriers for allergen-specific immunotherapy (AIT). In this study, we assessed efficacy of GNPs and dendritic cells (DC)-specific aptamer-modified GNPs (Apts-GNP) for epicutaneous immunotherapy (EPIT) in the case of pollen allergen extracts containing a variety of allergenic and non-allergenic components.

methodsBALB/c mice were sensitized to the total protein extract of Platanus orientalis pollen and epicutaneously treated in different groups either with free P. orientalis total pollen extract, naked GNPs, total extract loaded GNPs, and total extract loaded Apts-GNPs with and without skin-penetrating peptides (SPPs). Then, the specific IgE level (sIgE), total IgE concentration (tIgE) in the serum sample, IL-4, IL-17a, IFN-γ, and IL-10 cytokine concentrations in re-stimulated splenocytes with the total extract and mixture of recombinant allergens, nasopharyngeal lavage fluid (NALF) analysis, and histopathological analysis of lung tissue were evaluated.

resultsThis study indicated the total extract-loaded GNPs, especially Pla. ext (50 μg)-GNPs, significantly decreased sIgE, tIgE, IL-17a, and IL-4 concentrations, immune cells and eosinophils infiltration in NALF, and increased IL-10 and IFN-γ concentrations compared with the PBS-treated group. In addition, the histopathological analysis of lung tissue showed a significant decrease in allergic inflammation and histopathological damage. The DC-targeted group revealed the most significant improvement in allergic-related immune factors with no histopathological damage compared with the same dose without aptamer.

conclusionLoading total protein extract on the GNPs and the Apt-modified GNPs could be an effective approach to improve EPIT efficacy in a pollen-induced allergic mouse model.

Indexed as

AllergensAptamers, NucleotideCytokinesDendritic CellsDisease Models, AnimalGoldMetal NanoparticlesMice, Inbred BALB CPollenAdministration, CutaneousAnimalsAntigens, PlantDesensitization, ImmunologicFemaleHumansImmunoglobulin EAllergensAntigens, PlantAptamers, NucleotideCytokinesGoldImmunoglobulin EAllergic rhinitisAptamerEpicutaneous immunotherapyGold nanoparticlesPollen allergySkin penetrating peptide

Identifiers

PMID38091227
OpenAlexW4389675154

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Registered trials

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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.