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The human Cell Line Activation Test (h-CLAT) is an in vitro skin sensitization assay adopted by the OECD as Test Guideline 442E. In the h-CLAT, 2,4-dinitrochlorobenzene (DNCB) is used as a positive control; however, DNCB is considered a poisonous substance under the Poisonous and Deleterious Substances Control Act in Japan since 2014 because of its high acute toxicity. Strict control, handling, and storage are required when using DNCB, which is a burden to the users.

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Background/aim: Regulatory T cells (Tregs) play a crucial role in inflammatory responses by regulating the activity of various immune cells. M2 macrophages induced by IL-10 and TGF-β exhibit anti-inflammatory functions and induce Treg differentiation. Although the beneficial effects of 3-bromo-4,5-dihydroxybenzaldehyde (BDB) on various diseases have been widely reported, the mechanisms, through which it alleviates allergic contact dermatitis (ACD) via Tregs and macrophages, are not well understood.

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Atopic dermatitis (AD) is among the most frequently encountered skin diseases, bothering a considerable number of patients. Today, corticosteroids and antihistamines are among the numerous drugs applied for the therapy of AD. However, lengthy use of them contributes to side effects, such as physiological changes in skin.

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Article Synopsis
  • Research on dendritic cell (DC) activation has mostly relied on animal models, highlighting the need for human-based in vitro models due to differences in DC types across species.
  • Scientists have created a full-thickness human skin tissue model with Langerhans cell (LC) and dermal dendritic cell (DDC) surrogates from human leukemia cell lines to study their activation.
  • When exposed to nickel sulfate or DNCB, the model showed significant increases in CD1a positive cells, indicating that these treatments trigger a response leading to DC migration and activation within a short time frame.
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Article Synopsis
  • Silica, titanium dioxide, and zinc oxide nanoparticles are commonly found in skin products, but their potential to cause skin sensitization, especially when combined with other sensitizers, is not well understood.
  • This study utilized various cellular assays to explore how these nanoparticles affect skin cells, focusing on keratinocytes and dendritic cells, both alone and in co-cultures.
  • Results showed that the effects of nanoparticles vary significantly depending on the cell type and their interactions, indicating that exposure to these NPs can enhance the skin's reaction to known sensitizers.
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