Materials Map

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (1/1 displayed)

  • 2016Triple co-culture cell model as an in vitro model for oral particulate vaccine systemscitations

Places of action

Chart of shared publication
Rossi, C. De
1 / 1 shared
Lehr, C-M.
1 / 1 shared
Boisen, Anja
1 / 62 shared
Rades, T.
1 / 1 shared
Gordon, S.
1 / 2 shared
Nielsen, Line Hagner
1 / 12 shared
Chart of publication period
2016

Co-Authors (by relevance)

  • Rossi, C. De
  • Lehr, C-M.
  • Boisen, Anja
  • Rades, T.
  • Gordon, S.
  • Nielsen, Line Hagner
OrganizationsLocationPeople

document

Triple co-culture cell model as an in vitro model for oral particulate vaccine systems

  • Rossi, C. De
  • Boyd, B.
  • Lehr, C-M.
  • Boisen, Anja
  • Rades, T.
  • Gordon, S.
  • Nielsen, Line Hagner
Abstract

A triple co-culture cell model of Caco-2 cells, dendritic cells and macrophages (Figure 1) has previously been developed for studying intestinal permeability in a state of inflammation [1],[2].The aim of this study was to investigate the applicability of this cell model for testing the immunostimulatory ability of particulate vaccine formulations designed for oral delivery. Levels of cytokine production in response to vaccine administration were measured following particulate vaccine administration, as an indication of dendritic cell and macrophage activation. Precursors of cubosomes containing the model antigen ovalbumin was spray dried to obtain a particulate vaccine model system for testing in the cell model. The precursors were shown to form cubosomes when dispersed in aqueous medium, and was therefore used as the vaccine formulation for testing on the co-cultures. After 11 days, the TEER values of the co-cultures were found to be 860-1340 Ω∙cm2; the formulations were incubated with the co-cultures at this time point. From confocal microscopy images, it was observed that the THP-1 cells (macrophages) migrated into the overlying Caco-2 cell monolayer when the co-cultures were incubated with particle formulations. This was not the case when incubating with ovalbumin solution or blank. The ELISA screening assay showed production of a wide range of cytokines following culture incubation with cubosomes (with and without ovalbumin) and LPS solutions, indicative of a stimulatory effect; this was not observed with ovalbumin and blank solution. An example of the results is shown in Figure 2 for IL-17A. An established co-culture of Caco-2, THP-1 and MUTZ-3 cells showed promise as an in vitro model for testing of oral vaccine formulations. Mobility of co-culture immune cells as well as cytokine production observed following treatment with spray dried cubosomes as a particulate vaccine formulation will be further investigated. <br/>

Topics
  • impedance spectroscopy
  • mobility
  • permeability
  • activation
  • confocal microscopy