Evidence map›Paper›PMID 37897225›Full record

ArticleJournal of applied toxicology : JAT2024

The inter-laboratory validation study of EpiSensA for predicting skin sensitization potential.

Hideyuki Mizumachi, Mika Watanabe, Mayu Ikezumi, Michika Kajiwara, Michiyo Yasuda, Makoto Mizuno, Noriyasu Imai, Megumi Sakuma, Momoko Shibata, Shin-Ichi Watanabe and 11 more

Open access · greenAbstract read
In one paragraph

Article in Journal of applied toxicology : JAT, 2024. 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
1.4field-weighted citation impact, top 17% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
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

21 authors at 10 institutions in 5 countries.

Hideyuki MizumachiR&D Safety Science Research, Kao Corporation, 2606 Akabane, Ichikai-Machi, Haga-Gun, Tochigi, 321-3497, Japan.ORCID 0000-0001-8778-1951
Mika WatanabeFood and Drug Safety Center, Hatano Research Institute, 729-5 Ochiai, Hadano, Kanagawa, 257-8523, Japan.
Mayu IkezumiFood and Drug Safety Center, Hatano Research Institute, 729-5 Ochiai, Hadano, Kanagawa, 257-8523, Japan.
Michika KajiwaraFood and Drug Safety Center, Hatano Research Institute, 729-5 Ochiai, Hadano, Kanagawa, 257-8523, Japan.
Michiyo YasudaFood and Drug Safety Center, Hatano Research Institute, 729-5 Ochiai, Hadano, Kanagawa, 257-8523, Japan.
Makoto MizunoSafety and Analytical Research Laboratories, KOSÉ Corporation, 48-18 Sakae-cho, Kita-ku, Tokyo, 114-0005, Japan.ORCID 0000-0002-2300-1618
Noriyasu ImaiSafety and Analytical Research Laboratories, KOSÉ Corporation, 48-18 Sakae-cho, Kita-ku, Tokyo, 114-0005, Japan.ORCID 0000-0003-1488-4292
Megumi SakumaSafety and Analytical Research Laboratories, KOSÉ Corporation, 48-18 Sakae-cho, Kita-ku, Tokyo, 114-0005, Japan.
Momoko ShibataSafety and Analytical Research Laboratories, KOSÉ Corporation, 48-18 Sakae-cho, Kita-ku, Tokyo, 114-0005, Japan.
Shin-Ichi WatanabeSafety Research Science Laboratory, LION Corporation, 100 Tajima, Odawara-shi, Kanagawa, 256-0811, Japan.
Junko MotoyamaSafety Research Science Laboratory, LION Corporation, 100 Tajima, Odawara-shi, Kanagawa, 256-0811, Japan.
David BasketterDABMEB Consultancy Ltd., Kingswood, Gloucestershire, GL12 8RN, UK.
Chantra EskesServices and Consultation on Alternative Methods (SeCAM), Magliaso, Switzerland and Swiss 3R Competence Centre (3RCC), Bern, Switzerland.
Sebastian Hoffmannseh consulting + services, Stembergring 15, Paderborn, 33106, Germany.
David M LehmannOffice of Research and Development, US Environmental Protection Agency, 109 T.W. Alexander Drive, Research Triangle Park, NC, 27709, USA.
Takao AshikagaJapanese Center for the Validation of Alternative Methods (JaCVAM), National Institute of Health Sciences, 3-25-26 Tonomachi, Kawasaki-ku, Kanagawa, 210-9501, Japan.
Takashi SozuDepartment of Information and Computer Technology, Faculty of Engineering, Tokyo University of Science, Katsushika-ku, Tokyo, 125-0051, Japan.
Masahiro TakeyoshiChemicals Assessment and Research Center, Chemicals Evaluation and Research Institute (CERI), 1600 Shimotakano, Sugito-machi, Kitakatsushika-gun, Saitama, 345-0043, Japan.ORCID 0000-0001-8941-2076
Sho SuzukiR&D Safety Science Research, Kao Corporation, 2606 Akabane, Ichikai-Machi, Haga-Gun, Tochigi, 321-3497, Japan.
Masaaki MiyazawaR&D Safety Science Research, Kao Corporation, 2606 Akabane, Ichikai-Machi, Haga-Gun, Tochigi, 321-3497, Japan.
Hajime KojimaJapanese Center for the Validation of Alternative Methods (JaCVAM), National Institute of Health Sciences, 3-25-26 Tonomachi, Kawasaki-ku, Kanagawa, 210-9501, Japan.
Food and Drug Safety Center · JPKao Corporation (Japan) · JPLion Corporation (Japan) · JPNational Institute of Health Sciences · JPBH Consulting (Ireland) · IEChemicals Evaluation and Research Institute · JPEnvironmental Protection Agency · USFederal Roads Office · CHTokyo University of Science · JPWildfowl & Wetlands Trust · GB

Funding

Intramural EPA EPA999999Japan Agency for Medical Research and Development JP20mk0101131Japanese Society for Alternative to Animal ExperimentsLong-range Research Initiative by the Japan Chemical Industry Association
6 · The paper itself

Abstract

The Epidermal Sensitization Assay (EpiSensA) is a reconstructed human epidermis (RhE)-based gene expression assay for predicting the skin sensitization potential of chemicals. Since the RhE model is covered by a stratified stratum corneum, various kinds of test chemicals, including lipophilic ones and pre-/pro-haptens, can be tested with a route of exposure akin to an in vivo assay and human exposure. This article presents the results of a formally managed validation study of the EpiSensA that was carried out by three participating laboratories. The purpose of this validation study was to assess transferability of the EpiSensA to new laboratories along with its within- (WLR) and between-laboratory reproducibility (BLR). The validation study was organized into two independent stages. As demonstrated during the first stage, where three sensitizers and one non-sensitizer were correctly predicted by all participating laboratories, the EpiSensA was successfully transferred to all three participating laboratories. For Phase I of the second stage, each participating laboratory performed three experiments with an identical set of 15 coded test chemicals resulting in WLR of 93.3%, 93.3%, and 86.7%, respectively. Furthermore, when the results from the 15 test chemicals were combined with those of the additional 12 chemicals tested in Phase II of the second stage, the BLR for 27 test chemicals was 88.9%. Moreover, the predictive capacity among the three laboratories showed 92.6% sensitivity, 63.0% specificity, 82.7% accuracy, and 77.8% balanced accuracy based on murine local lymph node assay (LLNA) results. Overall, this validation study concluded that EpiSensA is easily transferable and sufficiently robust for assessing the skin sensitization potential of chemicals.

Indexed as

AllergensDermatitis, Allergic ContactAnimalsAnimal Testing AlternativesEpidermisHaptensHumansLocal Lymph Node AssayMiceReproducibility of ResultsSkinAllergensHaptensgene expressionlipophilic chemicalnon-animal test methodreconstructed human epidermisskin sensitizationvalidation study

Identifiers

PMID37897225
PMCPMC11503481
OpenAlexW4387996732

What OpenQuestion holds

Textmetadata
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.