Evidence map›Paper›PMID 29313026›Full record

ArticleBioengineering & translational medicine2017

Transcutaneous pollinosis immunotherapy using a solid-in-oil nanodispersion system carrying T cell epitope peptide and R848.

Momoko Kitaoka, Ayaka Naritomi, Yoshinori Kawabe, Masamichi Kamihira, Noriho Kamiya, Masahiro Goto

Abstract read
In one paragraph

Article in Bioengineering & translational medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
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  7. Editorial: The launch phase ofBioengineering & translational medicine · 2019
    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

6 authors.

Momoko KitaokaDept. of Applied Chemistry Kyushu University 744 Moto-oka Fukuoka 819-0395 Japan.
Ayaka NaritomiDept. of Applied Chemistry Kyushu University 744 Moto-oka Fukuoka 819-0395 Japan.
Yoshinori KawabeDept. of Chemical Engineering Kyushu University 744 Moto-oka Fukuoka 819-0395 Japan.
Masamichi KamihiraDept. of Chemical Engineering Kyushu University 744 Moto-oka Fukuoka 819-0395 Japan.
Noriho KamiyaDept. of Applied Chemistry Kyushu University 744 Moto-oka Fukuoka 819-0395 Japan.
Masahiro GotoDept. of Applied Chemistry Kyushu University 744 Moto-oka Fukuoka 819-0395 Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antigen-specific immunotherapy is the only curative approach for the treatment of allergic diseases such as Japanese cedar pollinosis. Immunotherapy using a T cell epitope vaccine in combination with the adjuvant R848 is of particular interest as a safe and effective approach to treat allergic diseases. Herein, we propose a simple and easy to handle vaccine administration method using the original solid-in-oil (S/O) nanodispersion system that permeates through the skin. The S/O nanodispersion system is composed of nanoparticles of hydrophilic molecules surrounded with hydrophobic surfactants that are dispersed in an oil vehicle. The system has potential to carry and deliver both hydrophilic and hydrophobic bioactives. Hydrophilic T cell epitope peptide was efficiently delivered through mouse skin using the S/O nanodispersion system and lowered antigen-specific IgE levels in pollinosis model mice. Addition of the hydrophobic adju1vant R848 significantly lowered the antibody secretion and shifted the Th1/Th2-balance toward Th1-type immunity in the model mice, showing the potential to alleviate Japanese cedar pollinosis.

Indexed as

immunotherapyR848Resiquimodsolid‐in‐oil nanodispersionT cell epitopetranscutaneous drug delivery

Identifiers

PMID29313026
PMCPMC5689524

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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.