Publications by authors named "J M Ovigne"

The U-SENS™ assay, formerly known as MUSST (Myeloid U937 Skin Sensitization Test), is an in vitro method to assess skin sensitization. Dendritic cell activation following exposure to sensitizers was modelled in the U937 human myeloid cell line by measuring the induction of the expression of CD86 by flow cytometry. The predictive performance of U-SENS™ was assessed via a comprehensive comparison analysis with the available human and LLNA data of 175 substances.

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Allergic contact dermatitis is a delayed-type hypersensitivity reaction induced by small reactive chemicals (haptens). Currently, the sensitising potential and potency of new chemicals is usually characterised using data generated via animal studies, such as the local lymph node assay (LLNA). There are, however, increasing public and political concerns regarding the use of animals for the testing of new chemicals.

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The sensitizing potential of chemicals is usually identified and characterized using one of the available animal test methods, such as the mouse local lymph node assay. Due to the increasing public and political concerns regarding the use of animals for the screening of new chemicals, the Colipa Skin Tolerance Task Force collaborates with and/or funds research groups to increase and apply our understanding of the events occurring during the acquisition of skin sensitization. Knowledge gained from this research is used to support the development and evaluation of novel alternative approaches for the identification and characterization of skin sensitizing chemicals.

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Regulatory policies in Europe prohibited the testing of cosmetic ingredients in animals for a number of toxicological endpoints. Currently no validated non-animal test methods exist for skin sensitization. Evaluation of changes in cell surface marker expression in dendritic cell (DC)-surrogate cell lines represents one non-animal approach.

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Article Synopsis
  • The 7th amendment of the EU Cosmetics Directive banned animal testing for eye irritation in cosmetics starting March 11th, 2009, prompting the search for alternative testing methods.
  • Researchers utilized the SkinEthic HCE model to assess the eye irritancy of 102 cosmetic substances, establishing a prediction model that effectively classified irritants and non-irritants with high sensitivity and specificity.
  • The method was further validated with an expanded set of 435 substances, achieving over 82% accuracy and demonstrating its potential as a reliable in vitro tool for predicting eye irritancy, leading to collaborations for prospective validation.
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