TYK2 as a therapeutic target in the treatment of autoimmune and inflammatory diseases

Author:

Gonciarz Maciej1,Pawlak-Buś Katarzyna2,Leszczyński Piotr2,Owczarek Witold3

Affiliation:

1. Department of Gastroenterology & Internal Medicine, Military Institute of Medicine, Warsaw, Poland

2. Department of Rheumatology, Rehabilitation & Internal Medicine, University of Medical Sciences, Poznan, Poland

3. Department of Dermatology, Military Institute of Medicine, Warsaw, Poland

Abstract

JAKs are intracellular protein tyrosine kinases that, through activation of STATs, are responsible for signal transduction pathways that regulate cellular responses to numerous cytokines, growth factors and hormones in many different cells. JAK-STAT signaling plays a key role in regulating immune function, and cytokines – such as IL-23, IL-12 and type I interferons – are central to the pathogenesis of autoimmune diseases, including psoriasis, inflammatory bowel disease and systemic lupus erythematosus. Here the authors review the evidence for targeting TYK2 as a more specific approach to treating these conditions. TYK2 inhibitors are clinically effective in autoimmune and inflammatory diseases and may avoid some of the complications reported with nonselective JAK inhibitors.

Funder

Bristol Myers Squibb

Publisher

Future Medicine Ltd

Subject

Oncology,Immunology,Immunology and Allergy

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