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Depletion of FoxP3+ Tregs improves control of larval Echinococcus multilocularis infection by promoting co-stimulation and Th1/17 immunity.

Junhua WangStephan MüllerRenyong LinMyriam SiffertDominique A VuittonHao WenBruno Gottstein
Published in: Immunity, inflammation and disease (2017)
FoxP3+ Tregs appear as one of the key players in immune regulatory processes favoring (i) metacestode survival by inhibiting the maturation potential of co-stimulatory activity and (ii) T cell exhaustion (suppressing Th1/Th17-type immune responses). We showed as well that prospectively, targeting FoxP3+ Tregs could be an option to develop an immunotherapy against AE.
Keyphrases
  • regulatory t cells
  • immune response
  • dendritic cells
  • signaling pathway
  • toll like receptor
  • risk assessment
  • drug delivery
  • inflammatory response
  • aedes aegypti
  • human health
  • climate change
  • zika virus