the JAK-family of cytokine receptors consists of four members: JAK1, JAK2, JAK3 and TYK2 that have different association patterns to receptors and are part of the Signal Transducer and Activation of Transcription (JAK-STAT) pathway
some JAK inhibitors are selective for specific JAK enzymes, which may influence their efficacy and safety profiles
JAK3 inhibitors necessarily cause a loss or total absence of T cells and natural killer cells while leaving a normal amount of B cells
Potential use cases
Rheumatoid arthritis
Psoriatic arthritis
Juvenile idiopathic arthritis
Axial spondyloarthritis
Ulcerative colitis
Atopic dermatitis
Alopecia areata
Potential side effects
increased risk of infections (like shingles) - hence live vaccinations soon before starting Rx or concurrently are NOT recommended
increased risk of major cardiovascular problems, such as heart attack and stroke, cancer, blood clots, serious infections and death, as compared with tumour necrosis factor (TNF) inhibitors1)
elevated cholesterol
blood clots
hypertension
anaemia
headache
diarrhoea
increased blood creatine phosphokinase
in some cases, increased risk of certain cancers, particularly in older adults with rheumatoid arthritis
increases risk of acne 2.5-fold more than when atopic dermatitis patients are Rx with Th2 cytokine inhibitors
others
General contra-indications include
active tuberculosis and other severe infections
recent live vaccination
severe liver impairment (Child–Pugh score C)
pregnancy
most are not approved for children aged under 12 yrs
should generally be avoided in:
age 65 or over
those at increased risk of cardiovascular problems such as heart attacks or stroke (eg. including current or past long-time smokers)
those at increased risk of cancer
those with risk factors for DVT / PE
those who have not yet had zoster vaccination (should be done well before starting Rx)
JAK-STAT system inhibitors
pan-JAK inhibitors
baricitinib (Olumiant)
oral agent mainly used to Rx rheumatoid arthritis and is a disease-modifying antirheumatic drug (DMARD)
delgocitinib (Corectim)
treatment of atopic dermatitis
FDA in 2025 approved topical treatment of adults with moderate to severe chronic hand eczema
used for the treatment of rheumatoid arthritis, psoriatic arthritis, atopic dermatitis, ulcerative colitis, Crohn's disease, ankylosing spondylitis, and axial spondyloarthritis