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 AndrassyPublished 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.