Deriving a Continuous Point of Departure for Skin Sensitization Risk Assessment Using a Bayesian Network Model

被引:0
作者
Tourneix, Fleur [1 ]
Carron, Leopold [1 ]
Jouffe, Lionel [2 ]
Hoffmann, Sebastian [3 ]
Alepee, Nathalie [1 ]
机构
[1] LOreal, Res & Innovat, 1Eugene Schueller, F-93600 Aulnay Sous Bois, France
[2] Bayesia SAS, Parc Ceres,Batiment N 21,Rue Ferdinand Buisson, F-53810 Change, France
[3] Seh Consulting Serv, Stembergring 15, D-33106 Paderborn, Germany
关键词
skin sensitization; risk assessment; point of departure; Bayesian network; defined approach; MOLECULAR INITIATING EVENT; PEPTIDE REACTIVITY ASSAY; POTENCY ASSESSMENT; IN-VITRO; ACTIVATION; KERATINOSENS; PREDICTIVITY; FUTURE;
D O I
10.3390/toxics12080536
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Regulations of cosmetic ingredients and products have been the most advanced in embracing new approach methodologies (NAMs). Consequently, the cosmetic industry has assumed a forerunner role in the development and implementation of animal-free next-generation risk assessment (NGRA) that incorporates defined approaches (DAs) to assess the skin sensitization potency of ingredients. A Bayesian network DA predicting four potency categories (SkinSens-BN) was constructed against reference Local Lymph Node Assay data for a total of 297 substances, achieving a predictive performance similar to that of other DAs. With the aim of optimally informing risk assessment with a continuous point of departure (PoD), a weighted sum of the SkinSens-BN probabilities for four potency classes (non-, weak, moderate, and strong/extreme sensitizer) was calculated, using fixed weights based on associated LLNA EC3-values. The approach was promising, e.g., the derived PoDs for substances classified as non-sensitizers did not overlap with any others and 77% of PoDs were similar or more conservative than LLNA EC3. In addition, the predictions were assigned a level of confidence based on the probabilities to inform the evaluation of uncertainty in an NGRA context. In conclusion, the PoD derivation approach can substantially contribute to reliable skin sensitization NGRAs.
引用
收藏
页数:16
相关论文
共 52 条
[1]   Off to a Good Start? Review of the Predictivity of Reactivity Methods Modelling the Molecular Initiating Event of Skin Sensitization [J].
Alepee, Nathalie ;
Tourneix, Fleur ;
Singh, Akanksha ;
Ade, Nadege ;
Gregoire, Sebastien .
ALTEX-ALTERNATIVES TO ANIMAL EXPERIMENTATION, 2023, 40 (04) :606-618
[2]  
Alpe N., 2017, Alternatives for Dermal Toxicity Testing, P311
[3]  
[Anonymous], 2015, Globally Harmonized System of Classification and Labelling of Chemicals (GHS)
[4]  
[Anonymous], 2014, OECD SERIES TESTING, DOI DOI 10.1787/9789264221444-EN
[5]  
[Anonymous], 2003, CONTACT SENSITISATIO
[6]  
[Anonymous], 2009, European Commission Regulation (EC) No 1223/2009 of the European parliament and the council of 30 November 2009 on cosmetic products, VL342, P59
[7]  
Conrady S., 2015, Bayesian Networks BayesiaLabA Practical Introduction for Researchers, P382
[8]  
FAYYAD UM, 1993, IJCAI-93, VOLS 1 AND 2, P1022
[9]   Alternative Methods for Skin-Sensitization Assessment [J].
Gadarowska, Dominika ;
Kalka, Joanna ;
Daniel-Wojcik, Anna ;
Mrzyk, Inga .
TOXICS, 2022, 10 (12)
[10]   Read-across can increase confidence in the Next Generation Risk Assessment for skin sensitisation: A case study with resorcinol [J].
Gautier, Francoise ;
Tourneix, Fleur ;
Vandecasteele, Hind Assaf ;
van Vliet, Erwin ;
Bury, Dagmar ;
Alepee, Nathalie .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 2020, 117