Immunodepressive Effects of LPS on Monocyte CD14in Vivo
Having previously reported that septic patients displayed lower levels of monocyte CD14 (endotoxin receptor) as compared to normal individuals, we were interested in the hypothesis that lipopolysaccharide (LPS) modulates levels of monocyte CD14in vivo.We examined CD14 expression in 13 human voluntee...
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Published in | The Journal of surgical research Vol. 69; no. 1; pp. 7 - 10 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier Inc
01.04.1997
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Online Access | Get full text |
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Summary: | Having previously reported that septic patients displayed lower levels of monocyte CD14 (endotoxin receptor) as compared to normal individuals, we were interested in the hypothesis that lipopolysaccharide (LPS) modulates levels of monocyte CD14in vivo.We examined CD14 expression in 13 human volunteers who were given a non-lethal injection ofEscherichia coliLPS (4.0 ng/kg). Monocyte CD14 was assayed by direct immunofluorescent determination with appropriate anti-CD14 monoclonal antibodies using flow cytometry. To test for cell responsiveness, monocytes were additionally examined followingin vitrostimulation by phorbol myristate acetate (PMA) andN-formylmethionyl-leucyl-phenylalanine (FMLP). Following LPS infusion, all patients displayed significant monocytopenia and responded with fever and tachycardia. Plasma samples demonstrated elevated levels of TNFα. CD14 expression was down-regulated by 52% on monocytes obtained 3 hr following LPS infusion (P< 0.05, vs. pre-LPS levels). Monocytes obtained pre-LPS infusion were down-regulated followingin vitrostimulation by PMA to levels 72 ± 8% and by FMLP to levels 75 ± 5% of unstimulated control cells. In contrast, monocytes obtained 3 hr post-LPS infusion failed to respond to PMA or FMLP with significant down-regulation. LPS down-regulated CD14 expression on monocytesin vivoand LPS also blunted the ability of monocytes to respond to other stimuli. We conclude that LPS desensitizes monocytes to itself and thereby renders an immunodepressive effect on these cells. |
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ISSN: | 0022-4804 1095-8673 |
DOI: | 10.1006/jsre.1997.5010 |