House dust mite allergy: Its innate immune response and immunotherapy

Immunobiology. 2018 Mar;223(3):300-302. doi: 10.1016/j.imbio.2017.10.035. Epub 2017 Oct 16.

Abstract

Over the past few decades, allergic diseases have become increasingly prevalent worldwide. House dust mite (HDM) is the most important domestic source for allergic diseases such as allergic rhinitis, asthma and atopic dermatitis. Dermatophagoides pteronyssinus (Der p) is the major environmental allergen in southeast Asia because of the humid and warm environment is suitable for its growth. In the recent year, role of HDM allergen in allergic inflammation through innate immune system has been well studied. Toll-like receptors (TLRs), protease-activated receptors (PARs) and DC-SIGN could be activated by different HDM major allergens and proinflammatory cytokines also be upregulated. Treatment efficacy for HDM allergy is unsatisfied to the patients and the medication is limited. Immunotherapy provided an alternative option for treating HDM allergy through targeted to the mechanisms of allergic reaction and represented a long-term symptoms relief. Gene specific immunotherapy was currently being developed and it could decrease allergic inflammation and improve the efficacy of treatment. In this report, we reviewed recent studies about the role of HDM allergy in innate immune system and its immunotherapy. Understanding the HDM allergen induced signal transduction pathway and developed allergen specific immunotherapy could help physicians to create precise diagnosis and solve unmet need in HDM allergy.

Keywords: House dust mite allergy; Immunotherapy; Innate immune response.

Publication types

  • Review

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / therapeutic use
  • Antibodies, Monoclonal / therapeutic use
  • Antigens, Dermatophagoides / immunology
  • Antigens, Dermatophagoides / therapeutic use
  • Asthma / immunology*
  • Asthma / therapy
  • Dermatitis, Atopic / immunology*
  • Dermatitis, Atopic / therapy
  • Genetic Therapy
  • Humans
  • Immunity, Innate
  • Immunotherapy / methods*
  • Lymphocyte Antigen 96 / immunology
  • Molecular Targeted Therapy
  • Pyroglyphidae / immunology
  • Rhinitis, Allergic / immunology*
  • Rhinitis, Allergic / therapy
  • Signal Transduction

Substances

  • Anti-Inflammatory Agents
  • Antibodies, Monoclonal
  • Antigens, Dermatophagoides
  • Lymphocyte Antigen 96