Publication | Open Access
Discovery of a JAK3-Selective Inhibitor: Functional Differentiation of JAK3-Selective Inhibition over pan-JAK or JAK1-Selective Inhibition
187
Citations
21
References
2016
Year
Jak1 InhibitionImmunologyImmune RegulationInnate ImmunityInflammatory ArthritisImmune DysregulationInflammationSignaling PathwayReceptor Tyrosine KinaseInflammatory Rheumatic DiseaseInhibitory ActivityNovel TherapyJak-stat Signaling PathwayRheumatologyJak1-selective InhibitionAutoimmune DiseaseMechanism Of ActionChronic InflammationAutoimmunityHumoral ImmunityImmune-mediated Inflammatory DiseasesγC Cytokine SignalingPharmacologyInflammatory DiseaseCell BiologyCytokineSignal TransductionImmune Cell DevelopmentTh17 Cell DifferentiationFunctional DifferentiationJak3-selective InhibitionMedicineDrug Discovery
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.
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