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Immunology
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- ImmunologyOpen Access
Targeting Interleukin-2-inducible T-cell Kinase (ITK) and Resting Lymphocyte Kinase (RLK) Using a Novel Covalent Inhibitor PRN694
Journal of Biological ChemistryVol. 290Issue 10p5960–5978Published online: January 15, 2015- Yiming Zhong
- Shuai Dong
- Ethan Strattan
- Li Ren
- Jonathan P. Butchar
- Kelsey Thornton
- and others
Cited in Scopus: 33Background: ITK and RLK are unique to effector lymphocytes and critical for immune activation.Results: A novel selective covalent ITK/RLK inhibitor called PRN694 was discovered, which blocks T-cell and NK cell activation.Conclusion: PRN694 provides an effective tool to elucidate the roles of ITK and RLK in immune cell signaling.Significance: PRN694 could be an effective therapy for T-cell- or NK cell-driven autoimmune, inflammatory, and malignant diseases.