Human Toll-Like Receptor 2 Mediates Monocyte Activation by Listeria monocytogenes, But Not by Group B Streptococci or Lipopolysaccharide

• Published in: The Journal of immunology (1950) 2000-02, Vol.164 (4), p.2064-2069
• Main Authors: Flo, Trude H, Halaas, Oyvind, Lien, Egil, Ryan, Liv, Teti, Giuseppe, Golenbock, Douglas T, Sundan, Anders, Espevik, Terje
• Format: Article
• Language: English
• Subjects: Animals; Antibodies, Monoclonal - biosynthesis; Antigen-Antibody Reactions; CHO Cells; Cricetinae; Dose-Response Relationship, Immunologic; Drosophila Proteins; Epitopes - immunology; Hot Temperature; Humans; Interleukin-6 - antagonists & inhibitors; Interleukin-6 - biosynthesis; Lipopolysaccharide Receptors - physiology; Lipopolysaccharides - antagonists & inhibitors; Lipopolysaccharides - immunology; Listeria monocytogenes; Listeria monocytogenes - immunology; Macrophage Activation; Membrane Glycoproteins - immunology; Membrane Glycoproteins - physiology; Mice; Mice, Inbred BALB C; Monocytes - immunology; Monocytes - microbiology; NF-^KB protein; NF-B protein; NF-kappa B - metabolism; Receptors, Cell Surface - immunology; Receptors, Cell Surface - physiology; Streptococcus agalactiae - immunology; Toll-Like Receptor 2; Toll-Like Receptors; Transfection
• ISSN: 0022-1767; 1550-6606
• DOI: 10.4049/jimmunol.164.4.2064

Human Toll like receptor (TLR) 2 has been implicated as a signaling receptor for LPS from Gram-negative bacteria and cell wall components from Gram-positive organisms. In this study, we investigated whether TLR2 can signal cell activation by the heat-killed group B streptococci type III (GBS) and Listeria monocytogenes (HKLM). HKLM, but not GBS, showed a time- and dose-dependent activation of Chinese hamster ovary cells transfected with human TLR2, as measured by translocation of NF-kappaB and induction of IL-6 production. A mAb recognizing a TLR2-associated epitope (TL2.1) was generated that inhibited IL-6 production from Chinese hamster ovary-TLR2 cells stimulated with HKLM or LPS. The TL2.1 mAb reduced HKLM-induced TNF production from human monocytes by 60%, whereas a CD14 mAb (3C10) reduced the TNF production by 30%. However, coadministrating TL2.1 and 3C10 inhibited the TNF response by 80%. In contrast to this, anti-CD14 blocked LPS-induced TNF production from monocytes, whereas anti-TLR2 showed no inhibition. Neither TL2.1 nor 3C10 affected GBS-induced TNF production. These results show that TLR2 can function as a signaling receptor for HKLM, possibly together with CD14, but that TLR2 is unlikely to be involved in cell activation by GBS. Furthermore, although LPS can activate transfected cell lines through TLR2, this receptor does not seem to be the main transducer of LPS activation of human monocytes. Thus, our data demonstrate the ability of TLR2 to distinguish between different pathogens.