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Plasma concentrations of secretory leukocyte protease inhibitor (SLPI) differ depending on etiology and severity in community-onset bloodstream infection

Lange, Anna, 1975- (författare)
Örebro universitet,Institutionen för medicinska vetenskaper,Department of Infectious Diseases
Cajander, Sara, 1980- (författare)
Örebro universitet,Institutionen för medicinska vetenskaper,Department of Infectious Diseases
Magnuson, Anders (författare)
School of Medical Sciences, Örebro University, Örebro, Sweden,Clinical Epidemiology and Biostatistics
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Sundén-Cullberg, Jonas (författare)
Karolinska Institutet
Strålin, Kristoffer (författare)
Karolinska Institutet
Hultgren, Olof, 1970- (författare)
Örebro universitet,Institutionen för medicinska vetenskaper,Department of Infectious Diseases, Karolinska University Hospital, Stockholm, Sweden; Department of Clinical Immunology and Transfusion Medicine, Faculty of Medicine and Health, Örebro University, Örebro, Sweden
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 (creator_code:org_t)
2019-05-14
2019
Engelska.
Ingår i: European Journal of Clinical Microbiology and Infectious Diseases. - : Springer. - 0934-9723 .- 1435-4373. ; 38:8, s. 1425-1434
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • The severity of bloodstream infections (BSI) depends on pathogen, source, and host factors. Secretory leukocyte protease inhibitor (SLPI) counteracts tissue damage, balances inflammation, and is increased in pneumonia and sepsis. We aimed to evaluate whether SLPI production differs depending on etiology, disease severity, and sex in BSI and to correlate SLPI with markers of inflammation and immunosuppression. Of the adult patients with BSI, 109 were included and sampled repeatedly, from hospital admission through day 28. Controls (blood donors) were sampled twice. SLPI in plasma was measured with enzyme-linked immunosorbent assay (ELISA) technique. Streptococcus pneumoniae and Staphylococcus aureus etiology were associated with higher SLPI than Escherichia coli on days 1-2 and 3. On day 1-2, subjects with sepsis had higher SLPI concentrations than those with non-septic BSI. Pneumonia was associated with higher SLPI than a non-pulmonary source of infection. SLPI co-varied with inflammatory markers. SLPI concentrations did not differ with regard to sex in the full cohort, but men with pneumonia had higher SLPI than women on day 1-2. S. pneumoniae and S. aureus BSI were associated with higher SLPI, when compared to E. coli. Severity and pneumonia, as well as male sex in the pneumonia sub-cohort, were factors independently associated with higher SLPI.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Infektionsmedicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Infectious Medicine (hsv//eng)

Nyckelord

Bloodstream infection
SLPI
Secretory leukocyte protease inhibitor
Sepsis
Sepsis immunology

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