Abstract
Aberrant sensing of self-nucleic acids by Toll-like receptor (TLR) 7, 8, or 9 is associated with several autoimmune disorders, including systemic lupus erythematosus (SLE), rheumatoid arthritis, psoriasis, or systemic sclerosis. In recent years, several classes of synthetic oligonucleotides have been shown to antagonize sensing of immunostimulatory nucleic acids by TLR7/8/9, indicating that these molecules could have therapeutic applications in such autoimmune diseases. Conversely, synthetic oligonucleotides used in therapeutic technologies such as antisense and microRNA inhibitors also have the potential to inhibit TLR7/8/9 sensing, rendering patients more susceptible to viral/bacterial infections. This chapter describes a protocol to define the inhibitory activity of synthetic oligonucleotides on TLR7.
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Acknowledgments
The authors thank Frances Cribbin for her help with the redaction of this chapter and Soroush Sarvestani for performing the experiments shown in Fig. 1. The authors are supported by funding from the Australian NHMRC (1022144, 1062683 and 1081167 to MPG); the Australian Research Council (140100594 Future Fellowship to MPG); and the Victorian Government’s Operational Infrastructure Support Program.
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Ferrand, J., Gantier, M.P. (2016). Assessing the Inhibitory Activity of Oligonucleotides on TLR7 Sensing. In: McCoy, C. (eds) Toll-Like Receptors. Methods in Molecular Biology, vol 1390. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-3335-8_5
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DOI: https://doi.org/10.1007/978-1-4939-3335-8_5
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