Preston, Julie AEssilfie, Ama-TawiahHorvat, Jay CWade, Margaret ABeagley, Kenneth WGibson, Peter GFoster, Paul SHansbro, Phil M2015-12-080264-410Xhttp://hdl.handle.net/1885/30097Asthma is a common inflammatory disease of the airways. Current therapies alleviate symptoms but do not treat the disease. We aim to develop effective immunomodulatory therapies (IMTs) for asthma that target the underlying causes of disease based on Streptococcus pneumoniae (Spn). The effect of Spn IMT on the development of asthma [allergic airways disease (AAD)] was determined in mice. Killed Spn was administered before, during or after ovalbumin sensitization, and the subsequent development of AAD was assessed. IMT attenuated T cell cytokine production, goblet cell hyperplasia, airways hyperresponsiveness (AHR), and eosinophil numbers in the blood, bronchoalveolar lavage fluid and peribronchial tissue. This indicates the potential of Spn as an IMT for asthma.Keywords: ovalbumin; Pneumococcus vaccine; allergic airway disease; animal cell; animal experiment; animal model; animal tissue; article; asthma; cell count; cell hyperplasia; controlled study; cytokine production; eosinophil; female; goblet cell; immune response; Asthma; Immunomodulation; Streptococcus pneumoniaeInhibition of allergic airways disease by immunomodulatory therapy with whole killed Streptococcus pneumoniae200710.1016/j.vaccine.2007.09.0342015-12-08