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Gram‐negative bacteria induce proinflammatory cytokine production by monocytes in the absence of lipopolysaccharide (LPS)
Author(s) -
Uronen H.,
Williams A. J.,
Dixon G.,
Andersen S. R.,
Van Der Ley P.,
Van Deuren M.,
Callard R. E.,
Klein N.
Publication year - 2000
Publication title -
clinical & experimental immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.329
H-Index - 135
eISSN - 1365-2249
pISSN - 0009-9104
DOI - 10.1046/j.1365-2249.2000.01409.x
Subject(s) - proinflammatory cytokine , lipopolysaccharide , microbiology and biotechnology , cytokine , neisseria meningitidis , immunology , tumor necrosis factor alpha , bacteria , biology , monocyte , inflammation , genetics
Tumour necrosis factor‐alpha (TNF‐ α ), IL‐1 α and IL‐6 production by human monocytes in response to a clinical strain of the Gram‐negative encapsulated bacteria Neisseria meningitidis and an isogenic lpxA − strain deficient in LPS was investigated. Wild‐type N. meningitidis at concentrations between 10 5 and 10 8 organisms/ml and purified LPS induced proinflammatory cytokine production. High levels of these cytokines were also produced in response to the lpxA − strain at 10 7 and 10 8 organisms/ml. The specific LPS antagonist bactericidal/permeability‐increasing protein (rBPI 21 ) inhibited cytokine production induced by LPS and wild‐type bacteria at 10 5 organisms/ml but not at higher concentrations, and not by LPS‐deficient bacteria at any concentration. These data show that proinflammatory cytokine production by monocytes in response to N. meningitidis does not require the presence of LPS. Therapeutic strategies designed to block LPS alone may not therefore be sufficient for interrupting the inflammatory response in severe meningococcal disease.

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