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Infect. Immun., 01 1995, 104-109, Vol 63, No. 1
C Selig and W Nothdurft
To investigate the physiological role of granulocyte colony-stimulating
factor (G-CSF) and granulocyte-macrophage colony-stimulating factor (GM-
CSF) in the adaptation mechanisms of myelopoiesis to enhanced demand, we
studied both cytokines and their myeloid target cells in hematologically
healthy patients suffering from acute bacterial infections. Endogenous
serum levels of G-CSF and GM-CSF, granulocyte- macrophage colony-forming
cell (GM-CFC) concentrations, and differential counts were determined for
the peripheral blood of 57 patients with clinically apparent bacterial
infections (26 males and 31 females aged 16 to 89 years) and 18 healthy
controls (8 males and 10 females aged 23 to 84 years). Patients were
selected for acute-phase protein and at least two additional clinical signs
reflecting a bacterial infection. Patients showed significantly higher
numbers of myeloid progenitor cells than controls (median, 68 versus 26
GM-CFC/ml; P < or = 0.01). G-CSF but not GM-CSF levels were found to be
elevated (> or = 50 to 863 pg/ml). In the acute stage of infection,
progenitor and cytokine levels were not influenced by gender, differences
in therapy, or localization of the infection. Progenitor and G-CSF levels
were not associated with absolute neutrophil counts or C-reactive protein.
However, a negative correlation between number of GM-CFC per milliliter and
age (R = -0.47; P < or = 0.001) and an inverse relationship between the
incidence of high GM-CFC concentrations and elevated G-CSF levels (phi =
-0.34; P < or = 0.01) were found. Combining both parameters into a
cytokine-progenitor pattern, we observed a highly significant age-dependent
response of myelopoiesis to inflammation (P < or = 0.001). Younger
patients had high progenitor counts (> 75 GM-CFC/ml) associated with
G-CSF levels below 50 pg/ml, whereas for the older patients, the reverse
pattern was predominant. The results indicate that the age-dependent
myelopoietic response to acute bacterial infections is characterized by an
inverse relationship between progenitor cells and G-CSF. The observed
cytokine-progenitor patterns could have implications for therapy with G-CSF
and the prognosis of infectious diseases.
Copyright © 1995, American Society for Microbiology
Cytokines and progenitor cells of granulocytopoiesis in peripheral blood of patients with bacterial infections
Department of Clinical Physiology and Occupational Medicine, University of Ulm, Germany.
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