Surface Area- and Mass-Based Comparison of Fine and Ultrafine Nickel Oxide Lung Toxicity and Augmentation of Allergic Response in an Ovalbumin Asthma Model

Details

• Personal Author:
  Anderson, Stacey E. ; Kashon M ; Kodali V ; Roach KA ; Roberts, Jennifer R. ; Shane HL ; Stefaniak, Aleksandr B.
• Description:
  Background: The correlation of physico-chemical properties with mechanisms of toxicity has been proposed as an approach to predict the toxic potential of the vast number of emerging nanomaterials. Although relationships have been established between properties and the acute pulmonary inflammation induced by nanomaterials, properties' effects on other responses, such as exacerbation of respiratory allergy, have been less frequently explored. Methods: In this study, the role of nickel oxide (NiO) physico-chemical properties in the modulation of ovalbumin (OVA) allergy was examined in a murine model. Results: 181nm fine (NiO-F) and 42nm ultrafine (NiO-UF) particles were characterized and incorporated into a time course study where measured markers of pulmonary injury and inflammation were associated with NiO particle surface area. In the OVA model, exposure to NiO, irrespective of any metric was associated with elevated circulating total IgE levels. Serum and lung cytokine levels were similar with respect to NiO surface area. The lower surface area was associated with an enhanced Th2 profile, whereas the higher surface area was associated with a Th1-dominant profile. Surface area-normalized groups also exhibited similar alterations in OVA-specific IgE levels and lung neutrophil number. However, lung eosinophil number and allergen challenge-induced alterations in lung function related more to particle size, wherein NiO-F was associated with an increased enhanced pause response and NiO-UF was associated with increased lung eosinophil burden. Conclusions: Collectively, these findings suggest that although NiO surface area correlates best with acute pulmonary injury and inflammation following respiratory exposure, other physico-chemical properties may contribute to the modulation of immune responses in the lung. [Description provided by NIOSH]
• Subjects:
  Hypersensitivity Immune System Laboratories Lung Occupational Health Particulate Matter Respiratory System Safety Toxicology
• Keywords:
  Allergic Reactions Author Keywords: Nanotoxicology Immune Reaction Immune Response Laboratory Animals Lung Function Nanomaterials Nanotoxicology Nickel Oxide Nickel Oxide Nanoparticles Ovalbumin Allergy Model Particle Size Ultrafine Particles

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• ISSN:
  0895-8378
• Document Type:
  Text
• Genre:
  Journal Article
• Place as Subject:
  OSHA Region 3 ; West Virginia
• CIO:
  National Institute for Occupational Safety and Health (NIOSH)
• Division:
  HELD - Health Effects Laboratory Division ; RHD - Respiratory Health Division
• Topic:
  Workplace Safety & Health
• Location:
  North America
• Pages in Document:
  299-324
• Volume:
  31
• Issue:
  8
• NIOSHTIC Number:
  nn:20057885
• Citation:
  Inhal Toxicol 2019 Jul; 31(8):299-324
• Contact Point Address:
  Katherine A. Roach, Allergy and Clinical Immunology Branch (ACIB), National Institute of Occupational Safety and Health (NIOSH), 1095 Willowdale Road, Morgantown, WV 26505, USA
• Email:
  WVQ1@cdc.gov
• CAS Registry Number:
  Nickel monoxide (CAS RN 1313-99-1)
• Federal Fiscal Year:
  2019
• NORA Priority Area:
  Manufacturing
• Peer Reviewed:
  True
• Source Full Name:
  Inhalation Toxicology
• Collection(s):
  National Institute for Occupational Safety and Health
• Main Document Checksum:
  urn:sha-512:f4ec045ae7766b92d2a56e63e7b93b9e9eb0fc5f9e3392196afecf5bc87c14e8d5a8f8fef940004567b0cad51e365bc9e337866f9f774e031b525e8bb9231a6b
• Download URL:
  https://stacks.cdc.gov/view/cdc/215091/cdc_215091_DS1.pdf
• File Type:
  [PDF - 5.16 MB ]