| Literature DB >> 27791347 |
Jean-Baptiste Telliez1, Martin E Dowty2, Lu Wang1, Jason Jussif1, Tsung Lin1, Li Li1, Erick Moy1, Paul Balbo1, Wei Li1, Yajuan Zhao1, Kimberly Crouse1, Caitlyn Dickinson1, Peter Symanowicz1, Martin Hegen1, Mary Ellen Banker3, Fabien Vincent3, Ray Unwalla4, Sidney Liang5, Adam M Gilbert5, Matthew F Brown5, Matthew Hayward5, Justin Montgomery5, Xin Yang2, Jonathan Bauman2, John I Trujillo5, Agustin Casimiro-Garcia4, Felix F Vajdos5, Louis Leung2, Kieran F Geoghegan5, Amira Quazi1, Dejun Xuan1, Lyn Jones4, Erik Hett4, Katherine Wright2, James D Clark1, Atli Thorarensen4.
Abstract
PF-06651600, a newly discovered potent JAK3-selective inhibitor, is highly efficacious at inhibiting γc cytokine signaling, which is dependent on both JAK1 and JAK3. PF-06651600 allowed the comparison of JAK3-selective inhibition to pan-JAK or JAK1-selective inhibition, in relevant immune cells to a level that could not be achieved previously without such potency and selectivity. In vitro, PF-06651600 inhibits Th1 and Th17 cell differentiation and function, and in vivo it reduces disease pathology in rat adjuvant-induced arthritis as well as in mouse experimental autoimmune encephalomyelitis models. Importantly, by sparing JAK1 function, PF-06651600 selectively targets γc cytokine pathways while preserving JAK1-dependent anti-inflammatory signaling such as the IL-10 suppressive functions following LPS treatment in macrophages and the suppression of TNFα and IL-1β production in IL-27-primed macrophages. Thus, JAK3-selective inhibition differentiates from pan-JAK or JAK1 inhibition in various immune cellular responses, which could potentially translate to advantageous clinical outcomes in inflammatory and autoimmune diseases.Entities:
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Year: 2016 PMID: 27791347 DOI: 10.1021/acschembio.6b00677
Source DB: PubMed Journal: ACS Chem Biol ISSN: 1554-8929 Impact factor: 5.100