4.6 Article

Skin sensitization to fragrance hydroperoxides: interplay between dendritic cells, keratinocytes and free radicals

Journal

BRITISH JOURNAL OF DERMATOLOGY
Volume 184, Issue 6, Pages 1143-1152

Publisher

OXFORD UNIV PRESS
DOI: 10.1111/bjd.19685

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Funding

  1. DEFCHEMSKALL Franco-German Collaborative International Research Project [ANR-15-CE15-0023-01]
  2. DEFCHEMSKALL Franco-German Collaborative International Research Project (DFG) [BL340/6-1]

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Skin sensitization to hydroperoxides from commonly used fragrances can lead to allergic reactions, possibly through radical intermediates. This study found clear individual differences in DC maturation induced by different hydroperoxides, suggesting small structural alterations translate into specific immune responses. Understanding the differing activation levels and frequencies of DCs by these compounds may provide insights into sensitization mechanisms.
Background Skin sensitization to hydroperoxides (R-OOHs) of the commonly used fragrance terpenes limonene, linalool and citronellol is frequently reported. ROOHs are believed to initiate the process leading to sensitization and allergic contact dermatitis through mechanisms involving radical intermediates. Thus, radical intermediates, keratinocytes and dendritic cells (DCs) may act in concert to initiate the process. Objectives To evaluate individual DC activation profiles by R-OOHs in the context of keratinocytes with regard to frequency, specificity and magnitude of upregulation. Methods We used 2D and 3D cocultures with keratinocytes/reconstructed human epidermis (RHE) and DCs to evaluate cell surface levels of the costimulatory molecules CD86, CD80 and the adhesion molecule CD54 on cocultured DCs. Analysis of radical formation from limonene hydroperoxides in RHE was performed using electron paramagnetic resonance combined with the spin trapping technique. Results R-OOHs induce donor-dependent DC activation. Major differences were found between the limonene-OOHs. Limonene-1-OOH was stronger with respect to both frequency and magnitude of response. Using a 3D coculture model, no DC activation was detected after topical application of 0.2% limonene-OOHs (20 mu g cm(-2)), while 1.2% limonene-1-OOH or 2% limonene-2-OOH induced DC activation. Furthermore, we demonstrated differences in the carbon and oxygen radicals formed from the limonene-OOHs using RHE, mimicking what may happen in vivo. Conclusions We report clear individual differences in DC maturation induced by the most important hydroperoxides. Response rates and magnitude of response both indicate that very small structural alterations in the hydroperoxides are translated into specific DC responses. In addition, we provide more insight into the amounts of hydroperoxides that can activate DCs and induce sensitization.

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