Connective tissue responses in acute community-acquired pneumonia

Abstract

Circulating connective tissue components including the aminoterminal propeptides of type III collagen (PIIINP), type I collagen (PINP) and hyaluronan were determined in patients hospitalised for pneumonia of suspected bacterial origin. Ninety patients were included, 64 of these were followed prospectively for up to 21 days after initiation of therapy. Serum PIIINP was determined by RIA, s-PINP by ELISA, and s-hyaluronan by a radiometric assay. S-PIIINP rose significantly above the zero value within 24h in both pneumococcal pneumonia ( T 0: 5.3μg/l, 95% CI: 2.7–8.1μg/l vs. T 1: 6.7μg/l, 95% CI: 3.8–9.1, P<0.01) and in pneumonia of unknown aetiology ( T 0: 4.0μg/l, 95% CI: 3.6–4.8 vs. T 1: 4.5μg/l, 95% CI: 3.8–5.1, P<0.05) followed by a gradual decline. At T 1, S-PIIINP was higher in pneumococcal pneumonia compared with pneumonia of unknown aetiology ( P<0.05). By contrast, s-PINP tended to decline within 24h in both pneumococcal pneumonia ( T 1: 30μg/l, 95 % CI: 23–40, ns) and in pneumonia of unknown aetiology ( T 1: 32μg/l, 95% CI: 22–42, ns) followed by a steady increase. The PINP antigen size distribution remained constant throughout the follow-up period. S-hyaluronan in pneumococcal pneumonia paralleled s-PIIINP reaching a peak value on day 1 (121μg/l, 95% CI: 65–191, P =0.38). There was a positive correlation between s-PIIINP and C-reactive protein (CRP). The study demonstrates, that community-acquired pneumonia elicits a differentiated mesenchymal response, which is turned down in response to successful antibiotic therapy.