Small Molecule Analogues of the parasitic worm product ES-62 interact with the TIR domain of MyD88 to inhibit pro-inflammatory signalling
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-018-20388-z.pdf
Reference44 articles.
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2. Pineda, M. A., Lumb, F., Harnett, M. M. & Harnett, W. ES-62, a therapeutic anti-inflammatory agent evolved by the filarial nematode Acanthocheilonema viteae. Molecular and Biochemical Parasitology 194, 1–8, https://doi.org/10.1016/j.molbiopara.2014.03.003 (2014).
3. McInnes, I. B. et al. A novel therapeutic approach targeting articular inflammation using the filarial nematode-derived phosphorylcholine-containing glycoprotein ES-62. J Immunol 171, 2127–2133 (2003).
4. Pineda, M. A. et al. The parasitic helminth product ES-62 suppresses pathogenesis in collagen-induced arthritis by targeting the interleukin-17-producing cellular network at multiple sites. Arthritis and Rheumatism 64, 3168–3178, https://doi.org/10.1002/art.34581 (2012).
5. Pineda, M. A., Rodgers, D. T., Al-Riyami, L., Harnett, W. & Harnett, M. M. ES-62 protects against collagen-induced arthritis by resetting interleukin-22 toward resolution of inflammation in the joints. Arthritis Rheumatol 66, 1492–1503, https://doi.org/10.1002/art.38392 (2014).
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