Abstract
Minimal concentration ranges of lipopolysaccharides, natural and synthetic lipid As, and partial structures were established for the induction of release of IL-1 and TNF from human MNC. LPS was more potent than lipid A. Partial structures of lipid A lacking nonhydroxylated fatty acids were inactive, but in combination with LPS or lipid A exhibited time-dependent synergistic or antagonistic effects.
MeSH terms
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Glycolipids / pharmacology
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Humans
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In Vitro Techniques
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Interleukin-1 / biosynthesis*
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Leukocytes, Mononuclear / drug effects
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Leukocytes, Mononuclear / immunology
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Leukocytes, Mononuclear / metabolism
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Lipid A / pharmacology
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Lipopolysaccharides / pharmacology*
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Tumor Necrosis Factor-alpha / biosynthesis*
Substances
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Glycolipids
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Interleukin-1
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Lipid A
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Lipopolysaccharides
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Tumor Necrosis Factor-alpha
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lipid X