AI Article Synopsis

  • - ES-62 is a protein from the filarial nematode Acanthocheilonema viteae with anti-inflammatory properties due to phosphorylcholine (PC) residues, suggesting potential for drug development in treating inflammatory diseases in humans.
  • - Two synthetic small molecule analogues, SMA 11a and SMA 12b, showed protective effects in a mouse model of acute allergic contact dermatitis by significantly reducing ear inflammation when administered before sensitization and challenge.
  • - Treatment with the SMAs reduced signs of inflammation, including cellular infiltration and collagen deposition in the ears, as well as lowering IFNγ mRNA levels, but had no effect on mast cell populations or other cytokines.

Article Abstract

ES-62 is the major secreted protein of the rodent filarial nematode Acanthocheilonema viteae. The molecule contains covalently attached phosphorylcholine (PC) residues, which confer anti-inflammatory properties on ES-62, underpinning the idea that drugs based on this active moiety may have therapeutic potential in human diseases associated with aberrant inflammation. Here we demonstrate that two synthetic small molecule analogues (SMAs) of ES-62 termed SMA 11a and SMA 12b are protective in the oxazolone-induced acute allergic contact dermatitis mouse model of skin inflammation, as measured by a significant reduction in ear inflammation following their administration before oxazolone sensitisation and before oxazolone challenge. Furthermore, it was found that when tested, 12b was effective at reducing ear swelling even when first administered before challenge. Histological analysis of the ears showed elevated cellular infiltration and collagen deposition in oxazolone-treated mice both of which were reduced by treatment with the two SMAs. Likewise, the oxazolone-induced increase in IFNγ mRNA in the ears was reduced but no effect on other cytokines investigated was observed. Finally, no influence on the mast cell populations in the ear was observed.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4659540PMC
http://dx.doi.org/10.1016/j.exppara.2015.03.025DOI Listing

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