articleShockJul 28, 2006Closed access

HMGB1 SIGNALS THROUGH TOLL-LIKE RECEPTOR (TLR) 4 AND TLR2

Feinstein Institute for Medical Research · Cornell University · +2 more institutions

PubMed
Indexed incrossrefpubmed

Abstract

In response to bacterial endotoxin (e.g., LPS) or endogenous proinflammatory cytokines (e.g., TNF and IL-1beta), innate immune cells release HMGB1, a late cytokine mediator of lethal endotoxemia and sepsis. The delayed kinetics of HMGB1 release makes it an attractive therapeutic target with a wider window of opportunity for the treatment of lethal systemic inflammation. However, the receptor(s) responsible for HMGB1-mediated production of proinflammatory cytokines has not been well characterized. Here we demonstrate that in human whole blood, neutralizing antibodies against Toll-like receptor 4 (TLR4, but not TLR2 or receptor for advanced glycation end product) dose-dependently attenuate HMGB1-induced IL-8…

Citation impact

826
total citations
FWCI
28.38
Percentile
100%
References
33
Citations per year

Authors

9

Topics & keywords

Keywords
  • HMGB1
  • TLR2
  • Proinflammatory cytokine
  • TLR4
  • Toll-like receptor
  • Cytokine
  • Rage (emotion)
  • Cell biology
UN Sustainable Development Goals
  • Good health and well-being
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