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Hemophagocytic macrophages constitute a major compartment of heme oxygenase expression in sepsis.

AbstractOBJECTIVES:
Uncontrolled macrophage activation with hemophagocytosis is a distinctive feature of hemophagocytic syndromes (HPS). We examined whether lympho-histiocytic infiltration of the bone marrow and liver, as well as hemo-/erythrophagocytosis also occurs during sepsis and whether this process could account for the increased production of anti-inflammatory heme-oxygenase (HO-1) products observed during sepsis.
METHODS:
Hemophagocytosis and expression of CD163, HO-1, ferritin as well as CD8 and granzyme-B were examined in post-mortem bone marrow samples from 28 patients with sepsis and from eight control patients.
RESULTS:
Comparison of samples from non-septic patients with samples from patients with fatal sepsis revealed that the latter group displayed dense lympho-histiocytic bone marrow infiltration with CD163(+)/HO-1(+)/ferritin(+) macrophages as well as with CD8(+) and granzyme-B(+) T-cells. Hemophagocytosis with prominent phagocytosis of erythroid cells was readily apparent in septic patients, implying that this process is a likely stimulus for the up-regulation of macrophage HO-1 expression.
CONCLUSIONS:
Lympho-histiocytic activation with hemophagocytosis is a shared pathophysiologic mechanism in HPS and sepsis. Furthermore, the association of hemophagocytosis with an increase in HO-1 expression may indicate a novel role for this apparently futile process as a negative regulator of inflammation.
AuthorsDominik J Schaer, Christian A Schaer, Gabriele Schoedon, Alexander Imhof, Michael O Kurrer
JournalEuropean journal of haematology (Eur J Haematol) Vol. 77 Issue 5 Pg. 432-6 (Nov 2006) ISSN: 0902-4441 [Print] England
PMID17044836 (Publication Type: Comparative Study, Journal Article)
Chemical References
  • Biomarkers
  • Heme Oxygenase-1
Topics
  • Adult
  • Aged
  • Aged, 80 and over
  • Biomarkers (metabolism)
  • Bone Marrow (enzymology, metabolism, pathology)
  • Erythroid Cells (enzymology, pathology)
  • Female
  • Gene Expression Regulation, Enzymologic (genetics)
  • Heme Oxygenase-1 (biosynthesis, genetics)
  • Humans
  • Liver (enzymology, pathology)
  • Macrophages (enzymology, pathology)
  • Male
  • Middle Aged
  • Phagocytosis (genetics)
  • Sepsis (enzymology, genetics, pathology)
  • Up-Regulation (genetics)

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