Author: ["Montserrat Camps","Thomas Rückle","Hong Ji","Vittoria Ardissone","Felix Rintelen","Jeffrey Shaw","Chiara Ferrandi","Christian Chabert","Corine Gillieron","Bernard Françon","Thierry Martin","Denise Gretener","Dominique Perrin","Didier Leroy","Pierre-Alain Vitte","Emilio Hirsch","Matthias P Wymann","Rocco Cirillo","Matthias K Schwarz","Christian Rommel"]
CITE.CC academic search helps you expand the influence of your papers.
Abstract
Phosphoinositide 3-kinases (PI3K) have long been considered promising drug targets for the treatment of inflammatory and autoimmune disorders as well as cancer and cardiovascular diseases. But the lack of specificity, isoform selectivity and poor biopharmaceutical profile of PI3K inhibitors have so far hampered rigorous disease-relevant target validation. Here we describe the identification and development of specific, selective and orally active small-molecule inhibitors of PI3Kγ (encoded by Pik3cg). We show that Pik3cg−/− mice are largely protected in mouse models of rheumatoid arthritis; this protection correlates with defective neutrophil migration, further validating PI3Kγ as a therapeutic target. We also describe that oral treatment with a PI3Kγ inhibitor suppresses the progression of joint inflammation and damage in two distinct mouse models of rheumatoid arthritis, reproducing the protective effects shown by Pik3cg−/− mice. Our results identify selective PI3Kγ inhibitors as potential therapeutic molecules for the treatment of chronic inflammatory disorders such as rheumatoid arthritis.Cite this article
Camps, M., Rückle, T., Ji, H. et al. Blockade of PI3Kγ suppresses joint inflammation and damage in mouse models of rheumatoid arthritis. Nat Med 11, 936–943 (2005). https://doi.org/10.1038/nm1284 