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Lipopolysaccharide‐Binding Protein Increases Toll‐like Receptor 4–Dependent Activation by NontypeableHaemophilus influenzae
Author(s) -
Irini Lazou Ahrén,
Anders Bjartell,
Arne Egesten,
Kristian Riesbeck
Publication year - 2001
Publication title -
the journal of infectious diseases
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/323398
Subject(s) - tlr2 , haemophilus influenzae , lipopolysaccharide binding protein , tlr4 , cd14 , microbiology and biotechnology , toll like receptor , receptor , lipopolysaccharide , biology , immunology , respiratory tract , flow cytometry , innate immune system , immune system , respiratory system , biochemistry , anatomy , antibiotics
Nontypeable Haemophilus influenzae (NTHi) is a common cause of respiratory tract infections. This study investigated the ability of NTHi to bind lipopolysaccharide-binding protein (LBP) derived from respiratory epithelial cells and the subsequent stimulation of transfected cells expressing membrane-bound CD14 and toll-like receptor 2 (TLR2) or TLR4. In the absence of LBP, NTHi at high concentrations (100 bacteria/epithelial cell) were required to induce signals through TLR2 and TLR4. Flow cytometry showed that NTHi in the stationary phase bound more LBP than did log-phase bacteria. Of interest, as few as 1 LBP-bearing bacterium/cell induced strong signaling through TLR4. In contrast, LBP bound to NTHi did not promote any increased signaling mediated by TLR2, compared with NTHi without LBP. These data suggest that, upon NTHi infection, low numbers of bacteria binding LBP may activate TLR4-bearing cells, such as alveolar macrophages, and consequently induce an inflammatory response.

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