作者
Natascha Roehlen,Antonio Saviano,Houssein El Saghire,Émilie Crouchet,Zeina Nehme,Fabio Del Zompo,Frank Jühling,Marine Oudot,Sarah Durand,François H.T. Duong,Sara Cherradi,Víctor González-Motos,Nuno Almeida,Clara Ponsolles,Laura Heydmann,Tessa Ostyn,Antonin Lallement,Patrick Pessaux,Emanuele Felli,Andrea Cavalli,Jacopo Sgrignani,Christine Thumann,Olga S. Koutsopoulos,Bryan C. Fuchs,Yujin Hoshida,Maike Hofmann,Mogens Vyberg,Birgitte Martine Viuff,Elisabeth D. Galsgaard,Greg Elson,Alberto Toso,Markus Meyer,Roberto Iacone,Tamás Schweighoffer,Geoffrey Teixeira,Solange Moll,Claudio De Vito,Tania Roskams,Irwin Davidson,Danijela Heide,Mathias Heikenwälder,Mirjam B. Zeisel,Joachim Lupberger,Laurent Mailly,Catherine Schuster,Thomas F. Baumert
摘要
Tissue fibrosis is a key driver of end-stage organ failure and cancer, overall accounting for up to 45% of deaths in developed countries. There is a large unmet medical need for antifibrotic therapies. Claudin-1 (CLDN1) is a member of the tight junction protein family. Although the role of CLDN1 incorporated in tight junctions is well established, the function of nonjunctional CLDN1 (njCLDN1) is largely unknown. Using highly specific monoclonal antibodies targeting a conformation-dependent epitope of exposed njCLDN1, we show in patient-derived liver three-dimensional fibrosis and human liver chimeric mouse models that CLDN1 is a mediator and target for liver fibrosis. Targeting CLDN1 reverted inflammation-induced hepatocyte profibrogenic signaling and cell fate and suppressed the myofibroblast differentiation of hepatic stellate cells. Safety studies of a fully humanized antibody in nonhuman primates did not reveal any serious adverse events even at high steady-state concentrations. Our results provide preclinical proof of concept for CLDN1-specific monoclonal antibodies for the treatment of advanced liver fibrosis and cancer prevention. Antifibrotic effects in lung and kidney fibrosis models further indicate a role of CLDN1 as a therapeutic target for tissue fibrosis across organs. In conclusion, our data pave the way for further therapeutic exploration of CLDN1-targeting therapies for fibrotic diseases in patients.