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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-alpha 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.
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Florian Heil
Roche (Switzerland)
Hiroaki Hemmi
Okayama University of Science
Hubertus Hochrein
Bavarian Nordic (United States)
Science
The University of Osaka
Japan Science and Technology Agency
Wellesley College
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Heil et al. (Mon,) studied this question.
synapsesocial.com/papers/69d56d2575589c71d767cf59 — DOI: https://doi.org/10.1126/science.1093620
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