Species-Specific Recognition of Single-Stranded RNA via Toll-like Receptor 7 and 8

Double-stranded ribonucleic acid (dsRNA) serves as a danger signal associated with viral infection and leads to stimulation of innate immune cells. In contrast, the immunostimulatory potential of single-stranded RNA (ssRNA) is poorly understood and innate immune receptors for ssRNA are unknown. We r...

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Veröffentlicht in:Science (American Association for the Advancement of Science) 2004-03, Vol.303 (5663), p.1526-1529
Hauptverfasser: Heil, Florian, Hemmi, Hiroaki, Hochrein, Hubertus, Ampenberger, Franziska, Kirschning, Carsten, Akira, Shizuo, Lipford, Grayson, Wagner, Hermann, Bauer, Stefan
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Sprache:eng
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Zusammenfassung:Double-stranded ribonucleic acid (dsRNA) serves as a danger signal associated with viral infection and leads to stimulation of innate immune cells. In contrast, the immunostimulatory potential of single-stranded RNA (ssRNA) is poorly understood and innate immune receptors for ssRNA are unknown. We report that guanosine (G)- and uridine (U)-rich ssRNA oligonucleotides derived from human immunodeficiency virus-1 (HIV-1) stimulate dendritic cells (DC) and macrophages to secrete interferon-α and proinflammatory, as well as regulatory, cytokines. By using Toll-like receptor (TLR)-deficient mice and genetic complementation, we show that murine TLR7 and human TLR8 mediate species-specific recognition of GU-rich ssRNA. These data suggest that ssRNA represents a physiological ligand for TLR7 and TLR8.
ISSN:0036-8075
1095-9203
DOI:10.1126/science.1093620