PLoS ONE (Jan 2015)

Cytokine Signature in Infective Endocarditis.

  • Izabella Rodrigues Araújo,
  • Teresa Cristina Abreu Ferrari,
  • Andréa Teixeira-Carvalho,
  • Ana Carolina Campi-Azevedo,
  • Luan Vieira Rodrigues,
  • Milton Henriques Guimarães Júnior,
  • Thais Lins Souza Barros,
  • Cláudio Léo Gelape,
  • Giovane Rodrigo Sousa,
  • Maria Carmo Pereira Nunes

DOI
https://doi.org/10.1371/journal.pone.0133631
Journal volume & issue
Vol. 10, no. 7
p. e0133631

Abstract

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Infective endocarditis (IE) is a severe disease with high mortality rate. Cytokines participate in its pathogenesis and may contribute to early diagnosis improving the outcome. This study aimed to evaluate the cytokine profile in IE. Serum concentrations of interleukin (IL)-1β, IL-6, IL-8, IL-10, IL-12 and tumor necrosis factor (TNF)-α were measured by cytometric bead array (CBA) at diagnosis in 81 IE patients, and compared with 34 healthy subjects and 30 patients with non-IE infections, matched to the IE patients by age and gender. Mean age of the IE patients was 47±17 years (range, 15-80 years), and 40 (50%) were male. The IE patients had significantly higher serum concentrations of IL-1β, IL-6, IL-8, IL-10 and TNF-α as compared to the healthy individuals. The median levels of IL-1β, TNF-α and IL-12 were higher in the IE than in the non-IE infections group. TNF-α and IL-12 levels were higher in staphylococcal IE than in the non-staphylococcal IE subgroup. There was a higher proportion of both low IL-10 producers and high producers of IL-1β, TNF-α and IL-12 in the staphylococcal IE than in the non-staphylococcal IE subgroup. This study reinforces a relationship between the expression of proinflammatory cytokines, especially IL-1β, IL-12 and TNF-α, and the pathogenesis of IE. A lower production of IL-10 and impairment in cytokine network may reflect the severity of IE and may be useful for risk stratification.