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Unbiased Quantitative Proteomics Reveals a Crucial Role of the Allergen Context for the Activation of Human Dendritic Cells.

Abstract
Worldwide, more than 1 billion people suffer from allergic diseases. However, until now it is not fully understood how certain proteins can induce allergic immune responses, while others cannot. Studies suggest that allergenicity is a process not only determined by properties of the allergen itself but also by costimulatory factors, that are not classically associated with allergic reactions. To investigate the allergenicity of the major birch pollen allergen Bet v 1 and the impact of adjuvants associated with pollen, e.g. lipopolysaccharide (LPS), we performed quantitative proteome analysis to study the activation of monocyte-derived dendritic cells (moDCs). Thus, we treated cells with birch pollen extract (BPE), recombinant Bet v 1, and LPS followed by proteomic profiling via high-performance liquid chromatography and tandem mass spectrometry (HPLC-MS/MS) using isobaric labelling. Enrichment and pathway analysis revealed the influence of regulated proteins especially in cytokine signalling and dendritic cell activation. We found highly regulated, but differentially expressed proteins after treatment with BPE and LPS, whereas the cellular response to Bet v 1 was limited. Our findings lead to the conclusion that Bet v 1 needs a specific "allergen context" involving cofactors apart from LPS to induce an immune response in human moDCs.
AuthorsL Strasser, H-H Dang, H Schwarz, C Asam, F Ferreira, J Horejs-Hoeck, C G Huber
JournalScientific reports (Sci Rep) Vol. 7 Issue 1 Pg. 16638 (11 30 2017) ISSN: 2045-2322 [Electronic] England
PMID29192156 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Allergens
  • Biomarkers
  • Cytokines
  • Lipopolysaccharides
  • NF-kappa B
  • Proteome
Topics
  • Allergens (immunology)
  • Analysis of Variance
  • Biomarkers
  • Computational Biology (methods)
  • Cytokines (metabolism)
  • Cytotoxicity, Immunologic
  • Dendritic Cells (immunology, metabolism)
  • Gene Ontology
  • Humans
  • Hypersensitivity (immunology, metabolism)
  • Immunophenotyping
  • Lipopolysaccharides (immunology)
  • Molecular Sequence Annotation
  • NF-kappa B (metabolism)
  • Proteome
  • Proteomics (methods)

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