Synergistic effect of Dermatophagoides pteronyssinus allergen and Escherichia coli lipopolysaccharide on human blood cells

PLoS One. 2018 Nov 9;13(11):e0207311. doi: 10.1371/journal.pone.0207311. eCollection 2018.

Abstract

Purpose: House dust mites Dermatophagoides pteronyssinus are the main source of major inhalatory allergens inducing inflammatory response. Mite extract contain both allergenic proteins and lipopolysaccharides (LPS). The main allergenic protein, Der p 2, is a functional homolog of sMD-2, a protein providing blood cell response on LPS. Der p 2 may restore the response to LPS in absence of MD-2, but its interaction with LPS in whole blood is unknown. We studied the effect of Der p 2 on LPS-mediated activation of human whole blood cells.

Methods: Interaction of Der p 2 and LPS was studied on eight healthy donors. The whole blood was incubated with extract of house dust mite Dermatophagoides pteronyssinus (DP-e), recombinant antigenic protein Der p 2 variant 5 (rDep 2), Escherichia coli lipopolysaccharide and their combination. Supernatants were collected for ELISA analysis of protein content. Activation degree was determined by change in concentration of TNF-α, IL-8, IL-1Ra cytokines and sMD-2 protein.

Results: extract of mite Dermatophagoides pteronyssinus (DP-e) possessed weak inherent activity and did not cause significant increase of cytokine production. Simultaneous activation of blood cells by LPS and DP-e led to considerable increase of pro-inflammatory cytokine production. We have shown the intrinsic inducing activity of Der p 2 allergen on sMD-2 protein and TNF-α cytokine expression.

Conclusions: Der p 2 allergen enhances the response of human whole blood cells to external LPS by inducing additional expression of LPS-transporting protein sMD-2. The obtained data show an important role of LPS contamination of allegrens in the progress of allergic inflammatory response.

MeSH terms

  • Adolescent
  • Adult
  • Animals
  • Antigens, Dermatophagoides / chemistry
  • Antigens, Dermatophagoides / pharmacology*
  • Arthropod Proteins / chemistry
  • Arthropod Proteins / pharmacology*
  • Blood Cells / metabolism*
  • Blood Cells / pathology
  • Cytokines / biosynthesis*
  • Dermatophagoides pteronyssinus / chemistry*
  • Escherichia coli / chemistry*
  • Female
  • Gene Expression Regulation / drug effects
  • Humans
  • Lipopolysaccharides / chemistry
  • Lipopolysaccharides / pharmacology*
  • Male

Substances

  • Antigens, Dermatophagoides
  • Arthropod Proteins
  • Cytokines
  • Dermatophagoides pteronyssinus antigen p 2
  • Lipopolysaccharides

Grants and funding

The authors received no specific funding for this work.