“…Second, we did not look for all confounders, which could have influenced survival and particularly the development of BOS. Lymphocytic bronchitis/bronchiolitis are recognized as classic immunological risk factors [24,25], and other non-immunological risk factors have been proposed, such as ischaemic reperfusion, early non-specific bronchial hyperresponsiveness, donor and recipient age, graft ischaemic time, gastro-oesophageal reflux and bacterial/fungal/non-CMV viral infections [26]. Due to our small cohort, a reliable statistical analysis for these risk factors was difficult.…”