4.6 Review

Progress on the development of human in vitro dendritic cell based assays for assessment of the sensitizing potential of a compound

期刊

TOXICOLOGY AND APPLIED PHARMACOLOGY
卷 236, 期 3, 页码 372-382

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.taap.2009.02.004

关键词

Animal alternative; U-937; THP-1; MUTZ-3; Monocyte derived dendritic cell; CD34+derived dendritic cell; Test; Research; Validation; Biomarker; Allergen; Irritant; EU Directive 76/768/EEC; Sensitizer; Non-sensitizer

资金

  1. Integrated project 'Novel Testing Strategies for In Vitro Assessment of Allergens [LSHB-CT-2005-018681]

向作者/读者索取更多资源

Allergic contact dermatitis is the result of an adaptive immune response of the skin to direct exposure to an allergen. Since many chemicals are also allergens, European regulations require strict screening of all ingredients in consumer products. Until recently, identifying a potential allergen has completely relied on animal testing (e.g.: Local Lymph Node Assay). In addition to the ethical problems, both the 7th Amendment to the Cosmetics Directive and REACH have stimulated the development of alternative tests for the assessment of potential sensitizers. This review is aimed at summarising the progress on cell based assays, in particular dendritic cell based assays, being developed as animal alternatives. Primary cells (CD34(+) derived dendritic cells, monocyte derived dendritic cells) as well as dendritic cell-like cell lines (THP-1, U-937, MUT-Z-3, KG-1, HL-60, and K562) are extensively described along with bionnarkers such as cell surface markers, cytokines, chemokines and kinases. From this review, it can be concluded that no single cell based assay nor single marker is yet able to distinguish all sensitizers from non-sensitizers in a test panel of chemicals, nor is it possible to rank the sensitizing potential of the test chemicals. This suggests that sensitivity and specificity may be increased by a tiered assay approach. Only a limited number of genomic and proteomic studies have been completed until now. Such studies have the potential to identify novel biomarkers for inclusion in future assay development. Although progress is promising, this review suggests that it may be difficult to meet the up and coming European regulatory deadlines. (C) 2009 Elsevier Inc. All rights reserved.

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