Pplase of Dermatophagoides farinae promotes ovalbumin-induced airway allergy by modulating the functions of dendritic cells in a mouse model

Sci Rep. 2017 Feb 27:7:43322. doi: 10.1038/srep43322.

Abstract

Our previous studies revealed that many proteins in addition to the known allergens of D. farinae have not been fully characterized. We observed that Pplase did not respond to serum collected from patients sensitized to D. farinae. In a mouse model, Pplase significantly enhanced airway hyperresponsiveness (AHR) and Th2 responses induced by ovalbumin (OVA) compared with mice treated with OVA alone. Moreover, exposure to Pplase significantly increased the expression of IRF4, CD80, CD83, MHCII and TNF-α in DC2.4 cells, which was abolished in the presence of a TLR4 inhibitor. In vitro T cell polarization experiments revealed that Pplase alone could not induce T cell polarization but enhanced T cell polarization together with OVA. In addition, transfer of Pplase-primed bone marrow-derived DCs (BMDCs) to naïve mice enhanced AHR and Th2 immune responses in mice sensitized to OVA. In conclusion, Pplase is not an allergen of D. farinae but can activate DC cells to facilitate OVA-induced allergic responses.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Allergens / administration & dosage
  • Animals
  • Antigens, CD / genetics
  • Antigens, CD / immunology
  • Arthropod Proteins / pharmacology*
  • B7-1 Antigen / genetics
  • B7-1 Antigen / immunology
  • Basic Helix-Loop-Helix Transcription Factors / genetics
  • Basic Helix-Loop-Helix Transcription Factors / immunology
  • CD83 Antigen
  • Cell Line
  • Dendritic Cells / drug effects
  • Dendritic Cells / immunology*
  • Dendritic Cells / pathology
  • Dendritic Cells / transplantation
  • Dermatophagoides farinae / chemistry
  • Dermatophagoides farinae / immunology*
  • Disease Models, Animal
  • Female
  • Gene Expression Regulation
  • Histocompatibility Antigens Class II / genetics
  • Histocompatibility Antigens Class II / immunology
  • Humans
  • Immunoglobulins / genetics
  • Immunoglobulins / immunology
  • Interferon Regulatory Factors / genetics
  • Interferon Regulatory Factors / immunology
  • Lung / drug effects
  • Lung / immunology
  • Lung / pathology
  • Macrophage Activation / drug effects
  • Macrophages, Alveolar / drug effects
  • Macrophages, Alveolar / immunology
  • Macrophages, Alveolar / pathology
  • Male
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / immunology
  • Mice
  • Middle Aged
  • Ovalbumin / administration & dosage
  • Peptidylprolyl Isomerase / pharmacology*
  • Receptors, Aryl Hydrocarbon / genetics
  • Receptors, Aryl Hydrocarbon / immunology
  • Respiratory Hypersensitivity / chemically induced
  • Respiratory Hypersensitivity / genetics
  • Respiratory Hypersensitivity / immunology*
  • Respiratory Hypersensitivity / pathology
  • Signal Transduction
  • Sulfonamides / pharmacology
  • Toll-Like Receptor 4 / antagonists & inhibitors
  • Toll-Like Receptor 4 / genetics
  • Toll-Like Receptor 4 / immunology
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / immunology

Substances

  • Ahr protein, mouse
  • Allergens
  • Antigens, CD
  • Arthropod Proteins
  • B7-1 Antigen
  • Basic Helix-Loop-Helix Transcription Factors
  • Histocompatibility Antigens Class II
  • Immunoglobulins
  • Interferon Regulatory Factors
  • Membrane Glycoproteins
  • Receptors, Aryl Hydrocarbon
  • Sulfonamides
  • Tlr4 protein, mouse
  • Toll-Like Receptor 4
  • Tumor Necrosis Factor-alpha
  • ethyl 6-(N-(2-chloro-4-fluorophenyl)sulfamoyl)cyclohex-1-ene-1-carboxylate
  • interferon regulatory factor-4
  • Ovalbumin
  • Peptidylprolyl Isomerase