Mechanisms of altered monocyte prostaglandin E2 production in severely injured patients
Department of Medicine, Division of Gastroenterology; Department of Surgery; Department of Molecular Genetics
Medical Subject Headings
Adult; Aged; Aged, 80 and over; Bacterial Infections; Burns; Dinoprostone; Female; Humans; Male; Middle Aged; Monocytes; Multiple Trauma; Plasminogen Activators; Prostaglandins E; T-Lymphocytes, Regulatory; Time Factors
Digestive System Diseases | Gastroenterology
Monocytes from immunosuppressed trauma (11 patients) and burn (12 patients) patients stimulated with muramyl dipeptide, a potent prostaglandin E2 (PGE2) secretagogue, showed twofold greater PGE2 production compared with normal controls or immunocompetent patients. Monocyte plasminogen activator production was markedly depressed and inversely correlated to patients' monocyte hyper PGE2 production. Levels of the PGE2-producing monocyte subset (selected as high-affinity Fc+ receptors) were progressively elevated after injury in immunosuppressed patients, reaching 65% to 80% of the total monocyte population (39% for normal controls). Although early T-suppressor (Ts) lymphocytes did not augment monocyte PGE2 secretion, Ts lymphocytes that appeared late (greater than 12 days after injury), during chronic infection, acted as monocyte PGE2 secretagogues. Posttraumatic increases in monocyte sensitivity to PGE2 secretagogues augmented the numbers of PGE2-secreting monocytes, and the appearance of Ts lymphocytes with PGE2 secretagogue activity may be responsible for elevated monocyte PGE2 production in immunosuppressed trauma patients.
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Citation: Arch Surg. 1988 Mar;123(3):293-9.