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

Author:

Heil Florian1234,Hemmi Hiroaki1234,Hochrein Hubertus1234,Ampenberger Franziska1234,Kirschning Carsten1234,Akira Shizuo1234,Lipford Grayson1234,Wagner Hermann1234,Bauer Stefan1234

Affiliation:

1. Institute of Medical Microbiology, Immunology and Hygiene, Technische Universität München, Trogerstr. 9, D - 81675 Munich, Germany.

2. Department of Host Defense, Research Institute for Microbial Diseases, Osaka University, 3-1 Yamada-oka, Suita, Osaka 565-0871, Japan.

3. ERATO, Japan Science and Technology Corporation, Osaka 565-0047, Japan.

4. Coley Pharmaceutical Group, Inc., 93 Worcester Street, Suite 101, Wellesley, MA 02481, USA

Abstract

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.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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