Project

Contribution of antigen-presenting cells, airway epithelial cells and innate immune cells in controlling house dust mite specific T lymphocyte immunity

Code
3G037014
Duration
01 January 2014 → 31 December 2019
Funding
Research Foundation - Flanders (FWO)
Research disciplines
  • Medical and health sciences
    • Laboratory medicine
    • Palliative care and end-of-life care
    • Regenerative medicine
    • Other basic sciences
    • Laboratory medicine
    • Palliative care and end-of-life care
    • Regenerative medicine
    • Other clinical sciences
    • Other health sciences
    • Nursing
    • Other paramedical sciences
    • Laboratory medicine
    • Palliative care and end-of-life care
    • Regenerative medicine
    • Other translational sciences
    • Other medical and health sciences
Keywords
antigen-presenting cells innate immune cells airway epithelial cells
 
Project description

Asthma is a chronic inflammatory disease of the airways that is seen increasingly in westernalized countries. Airway dendritic cells (DC) and epithelial cells play a crucial role in the process of allergic sensitization to house dust mite (HDM), leading to asthma. Moreover, the recruitment of innate cells in the vicinity of DCs helps development of allergic inflammation. So far, HDM-specific T cell responses to HDM have never been studied due to the absence of any specific tools. To be able to address specific T cell activation to HDM, the host lab has successfully generated a new mouse line (1-Der mice) in which almost all T cells react to Der p 1, one of the major allergens of HDM. The specific objective of this project is to further characterize the immune response to HDM allergen inhalation. We will examine where and with what kinetics the HDMspecific T lymphocyte response occurs upon first or repeated encounter with HDM. We will analyze which antigen presenting cell (sub)population is presenting HDM allergen to T cells in vivo. Finally, the precise contribution of the epithelium and the innate cells on generation of HDM-specific T cell immunity will be addressed. Defining in more detail how T lymphocyte differentiation occurs in response to HDM might allow us to understand the influence of environmental and genetic risk factors on allergy. The ultimate goal is to halt harmful T cell responses to allergens.