4.5 Article

Application of the adverse outcome pathway framework for investigating skin sensitization potential of nanomaterials using new approach methods

期刊

CONTACT DERMATITIS
卷 84, 期 2, 页码 67-74

出版社

WILEY
DOI: 10.1111/cod.13669

关键词

fullerene; immunotoxicity; nanomaterials; single-wall carbon nanotubes; skin sensitization; titanium dioxide

资金

  1. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico [001]
  2. Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior
  3. Coordination for the Improvement of Higher Education Personnel
  4. National Council for Scientific and Technological Development

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The study reveals that nanomaterials can easily internalize into keratinocytes cells, interact with skin proteins, and induce activation of U937 cells by increasing CD86 expression and modulating inflammatory cytokine production, leading to their classification as skin sensitizers in vitro. This highlights the importance of studying the immunotoxicity and skin sensitization potential of nanomaterials to anticipate possible human health risks and contribute toward the applicability of existing OECD testing guidelines.
Background Currently, there are considerable efforts to standardize methods for accurate assessment of properties and safety aspects of nanomaterials. However, immunomodulation effects upon skin exposure to nanomaterial have been negligibly explored. Objectives To investigate the immunotoxicity of single-wall carbon nanotubes, titanium dioxide, and fullerene using the current mechanistic understanding of skin sensitization by applying the concept of adverse outcome pathway (AOP). Methods Investigation of the ability of nanomaterials to interact with skin proteins using the micro-direct peptide reactivity assay; the expression of CD86 cell surface marker using the U937 cell activation test (OECD No. 442E/2018); and the effects of nanomaterials on modulating inflammatory response through inflammatory cytokine release by U937 cells. Results The nanomaterials easily internalized into keratinocytes cells, interacted with skin proteins, and triggered activation of U937 cells by increasing CD86 expression and modulating inflammatory cytokine production. Consequently, these nanomaterials were classified as skin sensitizers in vitro. Conclusions Our study suggests the potential immunotoxicity of nanomaterials and highlights the importance of studying the immunotoxicity and skin sensitization potential of nanomaterials to anticipate possible human health risks using standardized mechanistic nonanimal methods with high predictive accuracy. Therefore, it contributes toward the applicability of existing OECD (Organisation for Economic Co-operation and Development) testing guidelines for accurate assessment of nanomaterial skin sensitization potential.

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