Imperial College London

ProfessorCaetanoReis e Sousa

Faculty of MedicineDepartment of Immunology and Inflammation

Visiting Professor
 
 
 
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Contact

 

c.reisesousa

 
 
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Location

 

Wright Fleming WingSt Mary's Campus

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Summary

 

Publications

Citation

BibTex format

@article{Diebold:2006:10.1002/eji.200636617,
author = {Diebold, SS and Massacrier, C and Akira, S and Paturel, C and Morel, Y and Reis, e Sousa C},
doi = {10.1002/eji.200636617},
journal = {Eur J Immunol},
pages = {3256--3267},
title = {Nucleic acid agonists for Toll-like receptor 7 are defined by the presence of uridine ribonucleotides.},
url = {http://dx.doi.org/10.1002/eji.200636617},
volume = {36},
year = {2006}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - Toll-like receptor 7 (TLR7) mediates innate responses by responding to viral RNA in endocytic compartments. However, the molecular pattern recognised by TLR7 and whether it differs between RNA of viral and self origin remains unclear. Here, we identify nucleic acids that act as TLR7 agonists for mouse and human cells. We show that uridine and ribose, the two defining features of RNA, are both necessary and sufficient for TLR7 stimulation, and that short single-stranded RNA (ssRNA) act as TLR7 agonists in a sequence-independent manner as long as they contain several uridines in close proximity. Consistent with the notion that TLR7 lacks specificity for sequence motifs, we show that it is triggered equally efficiently by viral or self RNA delivered to endosomes. Our results support the notion that TLR7 recognises uracil repeats in RNA and that it discriminates between viral and self ligands on the basis of endosomal accessibility rather than sequence.
AU - Diebold,SS
AU - Massacrier,C
AU - Akira,S
AU - Paturel,C
AU - Morel,Y
AU - Reis,e Sousa C
DO - 10.1002/eji.200636617
EP - 3267
PY - 2006///
SN - 0014-2980
SP - 3256
TI - Nucleic acid agonists for Toll-like receptor 7 are defined by the presence of uridine ribonucleotides.
T2 - Eur J Immunol
UR - http://dx.doi.org/10.1002/eji.200636617
UR - https://www.ncbi.nlm.nih.gov/pubmed/17111347
VL - 36
ER -