کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5541313 | 1553723 | 2016 | 10 صفحه PDF | دانلود رایگان |
- 7C2C5Ag and rTsp53 possess capacity to induce Trichinella spiralis-influenced semi-mature status of dendritic cells (DCs).
- Weak activation of both kinases (ERK, p38) in stimulated DCs proved to be sufficient for Th2 polarisation in vitro.
- 7C2C5Ag and rTsp53 may contribute to a Th2 shift, an observed immunomodulatory effect of Trichinella ES L1 products.
Excretory-secretory antigens of Trichinella spiralis muscle larvae can induce the semi-matured status of rat dendritic cells. This may at least partly be the consequence of transient activation of extracellular signal-regulated kinases 1/2 (ERK1/2). Here we investigated the potential of several components of excretory-secretory antigens (native fraction containing 45, 49 and 53 kDa proteins and recombinant Tsp53, representing one of the constituents of this fraction) to demonstrate previously observed effects of excretory-secretory antigens on dendritic cells in vitro, characterised by establishment of a particular phenotype (very low MHC II expression, moderate CD86 expression and significant ICAM-1 expression) and functional properties (low production of pro-inflammatory cytokine IL-12p70, and high production of IL-10 and TGF-β). Dendritic cells activated by these components were able to provoke proliferation of naïve T cells and their polarisation towards Th2 and anti-inflammatory responses. The investigated antigens had almost the same capacity to induce IL-4 and IL-10 production from T cells as excretory-secretory antigens, but failed to induce significant TGF-β synthesis. It could be concluded that the investigated excretory-secretory antigens components can largely reproduce the immunomodulatory effects of the complete excretory-secretory antigens and therefore may be considered as molecules important for creation of the anti-inflammatory milieu achieved by the parasite.
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Journal: International Journal for Parasitology - Volume 46, Issues 13â14, December 2016, Pages 833-842