Abstract

BackgroundThe use of engineered nanoparticles (NP) is widespread and still increasing. There is a great need to assess their safety. Newly engineered NP enter the market in a large variety; therefore safety evaluation should preferably be in a high-throughput fashion. In vitro screening is suitable for this purpose. TiO2NP exist in a large variety (crystal structure, coating and size), but information on their relative toxicities is scarce. TiO2NP may be inhaled by workers in e.g. paint production and application. In mice, inhalation of TiO2NP increases allergic reactions. Dendritic cells (DC) form an important part of the lung immune system, and are essential in adjuvant activity. The present study aimed to establish the effect of a variety of TiO2NP on DC maturation in vitro. Two NP of different crystal structure but similar in size, uncoated and from the same supplier, were evaluated for their adjuvant activity in vivo.MethodsImmature DC were differentiated in vitro from human peripheral blood monocytes. Exposure effects of a series of fourteen TiO2NP on cell viability, CD83 and CD86 expression, and IL-12p40 and TNF-α production were measured. BALB/c mice were intranasally sensitized with ovalbumin (OVA) alone, OVA plus anatase TiO2NP, OVA plus rutile TiO2NP, and OVA plus Carbon Black (CB; positive control). The mice were intranasally challenged with OVA. OVA-specific IgE and IgG1 in serum, cellular inflammation in bronchoalveolar lavage fluid (BALF) and IL-4 and IL-5 production in draining bronchial lymph nodes were evaluated.ResultsAll NP dispersions contained NP aggregates. The anatase NP and anatase/rutile mixture NP induced a higher CD83 and CD86 expression and a higher IL-12p40 production in vitro than the rutile NP (including coated rutile NP and a rutile NP of a 10-fold larger primary diameter). OVA-specific serum IgE and IgG1 were increased by anatase NP, rutile NP, and CB, in the order rutile<anatase<CB. The three particles similarly increased IL-4 and IL-5 production by bronchial LN cells and eosinophils and lymphocytes in the BALF. Neutrophils were induced by rutile NP and CB but not by anatase NP.ConclusionsOur data show that measuring CD83 and CD86 expression and IL-12p40 and TNF-α production in DC in vitro may provide an efficient way to screen NP for potential adjuvant activity; future studies should establish whether this also holds for other NP. Based on antigen-specific IgE and IgG1, anatase NP have higher adjuvant activity than rutile NP, confirming our in vitro data. Other parameters of the allergic response showed a similar response for the two NP crystal structures. From the viewpoint of safe(r) by design products, rutile NP may be preferred over anatase NP, especially when inhalation exposure can be expected during production or application of the product.

Highlights

  • The use of engineered nanoparticles (NP) is widespread and still increasing

  • A series of TiO2 NP with different crystal structure, coating, and size were evaluated in the Dendritic cells (DC) maturation assay in order to evaluate their DC activation potency as measure for their safety from the viewpoint of safe(r) by design products, especially when inhalation exposure can be expected during production or application of the product

  • Here we have shown that in vitro anatase and anatase/ rutile TiO2 NP induced a higher expression of CD83 and CD86 and a higher production of IL-12p40, than rutile NP, suggesting that DC maturation is induced to a greater extent by anatase and anatase/rutile NP than by rutile NP

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Summary

Introduction

The use of engineered nanoparticles (NP) is widespread and still increasing. There is a great need to assess their safety. Engineered NP enter the market in a large variety; safety evaluation should preferably be in a high-throughput fashion. Dendritic cells (DC) form an important part of the lung immune system, and are essential in adjuvant activity. Developed NP enter the market frequently and in a large variety, safety evaluation should preferably provide results quickly and in a high-throughput fashion. DC maturation is an essential step in the adaptive immune response [8] and plays an important role in enhancing an allergic response after inhalation of diesel soot particles [9, 10] and particulate matter [11] and likely of TiO2 NP. In the present study DC maturation is used as in vitro screening assay to determine the activation potency of TiO2 NP

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