Abstract

During bacterial infections, damage-associated molecular patterns (DAMPs) and pathogen-associated molecular patterns (PAMPs) activate immune cells. Here, we investigated whether plasma and sputum levels of High Mobility Group Box 1 (HMGB1), a prototypic DAMP, are associated with disease severity and aetiology in community-acquired pneumonia (CAP). In addition, in patients with pneumococcal CAP, the impact of the level of sputum lytA DNA load, a PAMP, was investigated. We studied patients hospitalised for bacterial CAP (n = 111), and samples were collected at admission. HMGB1 was determined by enzyme-linked immunosorbent assays, and pneumococcal lytA DNA load was determined by quantitative polymerase chain reaction. Plasma and sputum HMGB1 levels did not correlate to disease severity (pneumonia severity index or presence of sepsis), but high sputum HMGB1 level was correlated to pneumococcal aetiology (p = 0.002). In pneumococcal pneumonia, high sputum lytA DNA load was associated with respiratory failure (low PaO2/FiO2 ratio; p = 0.019), and high sputum HMGB1 level was associated with bacteraemia (p = 0.006). To conclude, high sputum HMGB1 was not associated with severe disease, but with pneumococcal bacteraemia, indicating a potential role for HMGB1 in bacterial dissemination. High sputum lytA was associated with severe disease.

Highlights

  • High Mobility Group Box 1 (HMGB1) is a nuclear protein that can be actively released by immune cells[1] or passively released by dead or injured cells[2]

  • Levels of HMGB1 in lower respiratory secretions have been correlated to disease severity in chronic obstructive pulmonary disease (COPD)[13], asthma[14], cystic fibrosis[15], and acute lung injury in Legionella pneumophila pneumonia[16], as well as to low oxygenation index in patients with pneumonia caused by Pneumocystis jirovecii[17]

  • When combining the sputum HMGB1 levels and the sputum lytA DNA load, we found that patients with high sputum HMGB1 levels and high sputum lytA DNA load had significantly higher plasma interleukin 8 (IL-8) levels (p = 0.014) and significantly lower PaO2/FiO2 ratios (p = 0.043) compared to the remaining patients (Fig. 4)

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Summary

Introduction

High Mobility Group Box 1 (HMGB1) is a nuclear protein that can be actively released by immune cells[1] or passively released by dead or injured cells[2]. Both infections and injury can cause HMGB1 release[3,4]. During bacterial infections, PRRs are at the same time activated by pathogen-associated molecular patterns (PAMPs), i.e., microbial components[3]. It is still unclear how DAMPs and PAMPs co-vary and what their relative contributions are as triggers for inflammation in bacterial infections. We hypothesise that sputum HMGB1 and plasma HMGB1 levels correlate with plasma IL-8 in patients with bacterial CAP

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