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Gram-negative bacteria induce proinflammatory cytokine production by monocytes in the absence of lipopolysaccharide (LPS)

Uronen-Hansson, Heli LU ; Williams, A J ; Dixon, G ; Andersen, S R ; Van Der Ley, P ; Van Deuren, M ; Callard, R E and Klein, N (2000) In Clinical and Experimental Immunology 122(3). p.312-315
Abstract
Tumour necrosis factor-alpha (TNF-alpha), IL-1alpha 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 105 and 108 organisms/ml and purified LPS induced proinflammatory cytokine production. High levels of these cytokines were also produced in response to the lpxA- strain at 107 and 108 organisms/ml. The specific LPS antagonist bactericidal/permeability-increasing protein (rBPI21) inhibited cytokine production induced by LPS and wild-type bacteria at 105 organisms/ml but not at higher concentrations, and not by LPS-deficient bacteria at any... (More)
Tumour necrosis factor-alpha (TNF-alpha), IL-1alpha 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 105 and 108 organisms/ml and purified LPS induced proinflammatory cytokine production. High levels of these cytokines were also produced in response to the lpxA- strain at 107 and 108 organisms/ml. The specific LPS antagonist bactericidal/permeability-increasing protein (rBPI21) inhibited cytokine production induced by LPS and wild-type bacteria at 105 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. (Less)
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author
; ; ; ; ; ; and
publishing date
type
Contribution to journal
publication status
published
subject
in
Clinical and Experimental Immunology
volume
122
issue
3
pages
312 - 315
publisher
British Society for Immunology
external identifiers
  • wos:000165552400005
  • scopus:0034535949
ISSN
0009-9104
DOI
10.1046/j.1365-2249.2000.01409.x
language
English
LU publication?
no
id
f05af4fe-91ae-4b2d-997e-a170153a7af6 (old id 1296984)
alternative location
http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pubmed&pubmedid=11122234
date added to LUP
2016-04-01 12:26:44
date last changed
2022-01-27 03:49:39
@article{f05af4fe-91ae-4b2d-997e-a170153a7af6,
  abstract     = {{Tumour necrosis factor-alpha (TNF-alpha), IL-1alpha 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 105 and 108 organisms/ml and purified LPS induced proinflammatory cytokine production. High levels of these cytokines were also produced in response to the lpxA- strain at 107 and 108 organisms/ml. The specific LPS antagonist bactericidal/permeability-increasing protein (rBPI21) inhibited cytokine production induced by LPS and wild-type bacteria at 105 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.}},
  author       = {{Uronen-Hansson, Heli and Williams, A J and Dixon, G and Andersen, S R and Van Der Ley, P and Van Deuren, M and Callard, R E and Klein, N}},
  issn         = {{0009-9104}},
  language     = {{eng}},
  number       = {{3}},
  pages        = {{312--315}},
  publisher    = {{British Society for Immunology}},
  series       = {{Clinical and Experimental Immunology}},
  title        = {{Gram-negative bacteria induce proinflammatory cytokine production by monocytes in the absence of lipopolysaccharide (LPS)}},
  url          = {{http://dx.doi.org/10.1046/j.1365-2249.2000.01409.x}},
  doi          = {{10.1046/j.1365-2249.2000.01409.x}},
  volume       = {{122}},
  year         = {{2000}},
}