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    Intensive Care Med. 2002 Jul;28(7):981-4. Epub 2002 May 28.

    Low plasma granulocyte-macrophage colony stimulating factor is an indicator of poor prognosis in sepsis.

    Source

    Department of Immunology, Third Floor, Duncan Building, Daulby Street, Liverpool, L69 3GA, UK.

    Abstract

    OBJECTIVE:

    Monocyte dysfunction has been shown to be associated with adverse consequences in septic patients. The cytokine growth factor granulocyte-macrophage colony stimulating factor (GM-CSF) may be required for optimal monocyte function in these patients. The current study investigates whether plasma GM-CSF levels were significantly different in septic patients and whether there was an association with prognosis.

    DESIGN:

    Plasma samples were collected from all septic patients from day 1 of the diagnosis of sepsis for 3 days. Healthy volunteer plasma served as control samples. A novel enzyme-linked immuno-adsorbent assay was developed with suitable sensitivity for detection of GM-CSF in patient and normal plasma. APACHE II score, age, sex and outcome were determined for all patients.

    SETTING:

    A single centre study at the Royal Liverpool University Hospital in a medico-surgical 13 bed intensive care unit.

    PATIENTS:

    All septic patients (n = 53) fulfilling the criteria of the APCC for the diagnosis of sepsis, were recruited for the study with informed consent from day 1 of the diagnosis of sepsis and plasma GM-CSF measured on three consecutive days. Patients were excluded from the study if on immunosuppressive therapy. Normal healthy volunteers (n = 33) were included in the study to serve as controls.

    RESULTS:

    Plasma GM-CSF levels were statistically significantly depressed in patients who died compared with those who survived, who had levels comparable with healthy controls.

    CONCLUSIONS:

    The results indicate that low plasma GM-CSF is associated with adverse consequences for septic patients. The measurement of GM-CSF in the plasma of septic patients merits further study for use as a prognostic marker and also to identify the type of immunotherapy the patient may benefit from.

    PMID:
    12122541
    [PubMed - indexed for MEDLINE]

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