“…Case studies of serum markers for drug-induced IP demonstrated that both SP-A and SP-D exhibited changes consistent with IP during the active phases of disease. The collectin markers remained elevated for a prolonged period of time (in contrast to acute-phase reactant CRP), despite improvement in the findings of diagnostic imaging, possibly indicating that inflammation of lung stroma persisted (Miyata et al, 2002;Taniguchi et al, 2005;Tanimura et al, 2006) and were thus suggested in diagnosis of IP. Among CVD patients with IP and/or fibrosis as pulmonary complication possibly with an autoimmune aetiology, there have been reported cases of systemic scleroderma (SSc), scleroderma spectrum disorders, systemic lupus erythematosus, dermatomyositis, RA, polymyositis/dermatomyositis, Sjo¨gren's syndrome, and progressive systemic sclerosis (PSS) with concurrent elevation of serum SP-A and SP-D both during active and inactive phases of disease (Takahashi et al, 1995;Maeda et al, 2001;Ihn et al, 2002;Kuwano et al, 2002).…”