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Am J Physiol Lung Cell Mol Physiol 279: L25-L35, 2000;
1040-0605/00 $5.00
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Vol. 279, Issue 1, L25-L35, July 2000

Phenotypic characterization of alveolar monocyte recruitment in acute respiratory distress syndrome

Simone Rosseau, Peter Hammerl, Ulrich Maus, Hans-Dieter Walmrath, Hartwig Schütte, Friedrich Grimminger, Werner Seeger, and Jürgen Lohmeyer

Department of Internal Medicine, Justus-Liebig-University, 35385 Giessen, Germany

In 49 acute respiratory distress syndrome (ARDS) patients, the phenotype of alveolar macrophages (AMs) was analyzed by flow cytometry. Bronchoalveolar lavage (BAL) was performed within 24 h after intubation and on days 3-5, 9-12, and 18-21 of mechanical ventilation. The 27E10high/CD11bhigh/CD71low/ 25F9low/HLA DRlow/RM3/1low AM population in the first BAL indicated extensive monocyte influx into the alveolar compartment. There was no evidence of increased local AM proliferation as assessed by nuclear Ki67 staining. Sequential BAL revealed two distinct patient groups. In one, a decrease in 27E10 and CD11b and an increase in CD71, 25F9, HLA DR, and RM3/1 suggested a reduction in monocyte influx and maturation of recruited cells into AMs, whereas the second group displayed sustained monocyte recruitment. In the first BAL from all patients, monocyte chemoattractant protein (MCP)-1 was increased, and AMs displayed elevated MCP-1 gene expression. In sequential BALs, a decrease in MCP-1 coincided with the disappearance of monocyte-like AMs, whereas persistent upregulation of MCP-1 paralleled ongoing monocyte influx. A highly significant correlation between BAL fluid MCP-1 concentration, the predominance of monocyte-like AMs, and the severity of respiratory failure was noted.

alveolar macrophages; monocyte chemoattractant protein-1; fluorescence-activated cell sorting; cell surface molecules


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