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Lipoproteins can bind lipopolysaccharide (LPS) and decrease the LPS-stimulated production of pro-inflammatory cytokines. We investigated the effect of increased plasma concentrations of low-density-lipoproteins (LDL) on survival and cytokine production after a lethal challenge with either LPS or live Gram-negative bacteria in LDL receptor deficient mice (LDLR minus/minus). The LDLR minus/minus mice challenged with LPS had an eightfold increased LD50 when compared with the wild type controls (C57B1/6J), while tumor necrosis factor alpha (TNF alpha) and interleukin-1 alpha (IL-1 alpha) plasma concentrations were decreased twofold. LDLR minus/minus mice had significantly lower and delayed mortality than control mice after infection with Klebsiella pneumoniae. No differences in the outgrowth of bacteria in the organs were present between the two groups, while circulating cytokine concentrations were decreased twofold in LDLR minus/minus mice. In contrast, the LPS-stimulated in vitro production of cytokines by peritoneal macrophages of LDLR minus/minus mice was significantly increased compared with controls. This increase was associated with enhanced specific binding of LPS to the macrophages of LDLR minus/minus mice. In conclusion, endogenous LDL can protect against the lethal effects of endotoxin and Gram-negative infection. At least part of this protection is achieved through decreased in vivo production of pro-inflammatory cytokines, in spite of increased cytokine production capacity. (J. Clin. Invest. 1996. 97:1366-1372). Key words: lipopolysaccharide centered dot gram-negative infection centered dot tumor necrosis factor centered dot interleukin-1 centered dot low-density lipoproteins.

Copyright (C) 1996 The American Society for Clinical Investigation, Inc.