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The cathepsin-S/protease-activated receptor-(PAR)-2 axis drives chronic allograft vasculopathy and is a molecular target for therapeutic intervention.

Martin RyllYutian LeiMichael N ThomasMingming LiBernhard RenzUlrich WirthFlorian KühnAlexandr BazhinJens WernerHans-Joachim AndersJoachim Andrassy
Published in: Transplant immunology (2023)
In conclusion, our data indicate that inhibiting CatS and PAR-2 deficiency led to a marked reduction of neointima formation and associated inflammation in a murine heterotopic model for allograft vasculopathy.
Keyphrases
  • kidney transplantation
  • randomized controlled trial
  • oxidative stress
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  • signaling pathway
  • replacement therapy
  • single molecule