Evidence map›Paper›PMID 26851134›Full record

ArticleJournal of applied toxicology : JAT2016

Integrated decision strategies for skin sensitization hazard.

Judy Strickland, Qingda Zang, Nicole Kleinstreuer, Michael Paris, David M Lehmann, Neepa Choksi, Joanna Matheson, Abigail Jacobs, Anna Lowit, David Allen and 1 more

Erratum issuedAbstract read
In one paragraph

Article in Journal of applied toxicology : JAT, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing 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

35 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. The MAK collection for occupational health and safety · 2025
    Review
  5. Article
  6. Article
  7. Adverse effects in traditional and alternative toxicity tests.Regulatory toxicology and pharmacology : RTP · 2024
    Article
  8. Use ofFrontiers in toxicology · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Evaluation of skin sensitization induced by four ionic liquids.Journal of applied toxicology : JAT · 2022
    Article
  18. Laboratory Techniques for Identifying Causes of Allergic Dermatitis.Immunology and allergy clinics of North America · 2021
    Review
  19. Frontiers in pharmacology · 2021
    Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Judy StricklandILS, Research Triangle Park, North Carolina, 27709, USA.
Qingda ZangILS, Research Triangle Park, North Carolina, 27709, USA.
Nicole KleinstreuerILS, Research Triangle Park, North Carolina, 27709, USA.
Michael ParisILS, Research Triangle Park, North Carolina, 27709, USA.
David M LehmannEPA/NHEERL/EPHD/CIB, Research Triangle Park, North Carolina, 27709, USA.
Neepa ChoksiILS, Research Triangle Park, North Carolina, 27709, USA.
Joanna MathesonU.S. Consumer Product Safety Commission, Bethesda, Maryland, 20814, USA.
Abigail JacobsFDA/CDER, Silver Spring, Maryland, 20993, USA.
Anna LowitEPA/OCSPP/OPP/HED, Washington, District of Columbia, 20460, USA.
David AllenILS, Research Triangle Park, North Carolina, 27709, USA.
Warren CaseyNIH/NIEHS/DNTP/NICEATM, Research Triangle Park, North Carolina, 27709, USA.

Funding

Intramural NIH HHS Z99 ES999999NIEHS NIH HHS HHSN273201500010C
6 · The paper itself

Abstract

One of the top priorities of the Interagency Coordinating Committee for the Validation of Alternative Methods (ICCVAM) is the identification and evaluation of non-animal alternatives for skin sensitization testing. Although skin sensitization is a complex process, the key biological events of the process have been well characterized in an adverse outcome pathway (AOP) proposed by the Organisation for Economic Co-operation and Development (OECD). Accordingly, ICCVAM is working to develop integrated decision strategies based on the AOP using in vitro, in chemico and in silico information. Data were compiled for 120 substances tested in the murine local lymph node assay (LLNA), direct peptide reactivity assay (DPRA), human cell line activation test (h-CLAT) and KeratinoSens assay. Data for six physicochemical properties, which may affect skin penetration, were also collected, and skin sensitization read-across predictions were performed using OECD QSAR Toolbox. All data were combined into a variety of potential integrated decision strategies to predict LLNA outcomes using a training set of 94 substances and an external test set of 26 substances. Fifty-four models were built using multiple combinations of machine learning approaches and predictor variables. The seven models with the highest accuracy (89-96% for the test set and 96-99% for the training set) for predicting LLNA outcomes used a support vector machine (SVM) approach with different combinations of predictor variables. The performance statistics of the SVM models were higher than any of the non-animal tests alone and higher than simple test battery approaches using these methods. These data suggest that computational approaches are promising tools to effectively integrate data sources to identify potential skin sensitizers without animal testing. Published 2016. This article has been contributed to by US Government employees and their work is in the public domain in the USA.

Indexed as

AllergensAnimalsAnimal Testing AlternativesCell LineComputational BiologyDecision MakingDermatitis, Allergic ContactHumansLocal Lymph Node AssayMiceReproducibility of ResultsRisk AssessmentSkinXenobioticsAllergensXenobioticsallergic contact dermatitisDPRAh-CLATintegrated decision strategyKeratinoSensLLNAmachine learningskin sensitizationsupport vector machine

Identifiers

PMID26851134
PMCPMC4945438

What OpenQuestion holds

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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.