Evaluating innate immune memory in allergy and infection: this research investigated whether respiratory infections and allergen exposure induced a memory function in innate immune cells that predisposed individuals or asthma development.
![[Eva Kaufmann]](/research/sites/vp2www/files/uploaded_images/researchers/Kaufmann-Eva-700X700.jpeg)
Tier 2
Innate immune memory in asthma and the quest for targeted immunotherapies
Eva Kaufmann’s research explored a new concept in innate immunity, termed "innate immune memory", or "trained immunity". Her lab studied whether allergen exposure induced long-lasting epigenetic changes in hematopoietic stem cells and innate immune cells, such as monocytes. Such epigenetic reprogramming can be a reason why asthmatic individuals experience exacerbations and are more susceptible to severe clinical trajectories of respiratory infections.
Dr. Kaufmann’s lab further investigated if childhood respiratory infections induced similar reprogramming that render the individual more susceptible to allergic sensitization and asthma. To date, it is well established that childhood respiratory infections, especially in conjunction with repeated wheezing, are linked to increased risks of subsequent asthma development. Dr. Kaufmann hypothesized that an epigenetic memory function in the first responder cells, the innate immune cells, can be the casual link between those infections and asthma.
Conducting fundamental research on these hypotheses will help scientists and clinicians to better understand asthma pathogenesis and can ultimately lead to the development of specific immunotherapies against asthma.