“…However, they have stimulated the search for novel biomarkers that may complement the clinical information currently gathered from physical examination, lung function tests, and imaging procedures [ 3 ]. The established role of infection, inflammation, and immunity in the pathophysiology and the clinical progression of COPD has led to the identification of a number of biomarkers within these pathways, e.g., eosinophils, procalcitonin, neutrophil elastase, and serum amyloid A, which can be characterised from different biological matrices, blood, saliva, or sputum [ 3 , 4 , 5 , 6 ]. Though some of these biomarkers, e.g., eosinophils and procalcitonin, appear particularly promising to enhance clinical and therapeutic decisions in patients with stable COPD and AECOPD [ 7 ], the availability of additional biomarkers from routine laboratory tests might also further improve patient care in those settings that have limited access to expensive and complex analytical facilities.…”