DefinitionThis section has been translated automatically.
Janus kinase (JAK) inhibitors are orally administered, anti-inflammatory, selectively immunomodulating and antiproliferative agents. They inhibit intracellular signaling pathways that are of central importance in the network of inflammatory cytokines. Structurally, Janus kinase inhibitors are characterized by nitrogen heterocycles, which are often condensed.
If the JAK signaling pathway is blocked at the cellular level, this indirectly inhibits the cytokine pathways. This allows them to simultaneously block several inflammation-inducing cytokines, e.g. interleukin-6, interleukin-12, interleukin-13. Unlike classic direct cytokine inhibitors (biologics that only inhibit one specific cytokine, e.g. Il-13, Il-17, IL-23). Depending on which JAK receptor pair is blocked, a large number of cytokines are blocked. This leads to more side effects, but also to more possible applications.
Biologics (e.g. TNF-alpha antagonists) prevent inflammatory messengers from docking to specific cell receptors outside the cell. Janus kinase inhibitors have a broader effect because they modulate several cytokines at the same time by inhibiting the kinase pathway.
ClassificationThis section has been translated automatically.
There are four members of the JAK family:
The Janus kinase inhibitors have different selectivity.
The following preparations are currently available:
- Oclacitinib (Apoquel®) - veterinary medicinal product
Tofacitinib: The first member of this class, tofacitinib has been used for some time in the treatment of rheumatoid arthritis and psoriatic arthritis. Tofacitinib inhibits JAK1, JAK2, JAK3 and to a lesser extent TYK2 in vitro. It has functional specificity for JAK1 and JAK3 over JAK2. Regarding the mechanism of action, it is known that tofacitinib reversibly and competitively inhibits the ATP binding site of JAKs. Without ATP, the JAKs cannot phosphorylate other proteins. Approval status 8/22 RA,PsA,ankylosing spondylitis,ulcerative colitis,polyarticular JIA and juvenile PsA children and adolescents 2-18 years.
Baricitinib: strongly blocks JAK1 and JAK2 kinases. Approval: AD, RA, alopecia areata.
Fedratinib is a JAK2-selective inhibitor that has a higher potency for JAK2 than for the other members of the JAK family (JAK1, JAK3 and TYK2). Abnormal activation of JAK2 is associated with myeloproliferative neoplasms, including myelofibrosis and polycythaemia vera. Fedratinib is indicated for the treatment of disease-related splenomegaly (spleen enlargement) or symptoms in adult patients with primary myelofibrosis (MF), post-polycythaemia vera myelofibrosis (post-PV-MF) or post-essential thrombocythemia myelofibrosis (post-ET-MF) who have not yet received a Janus kinase (JAK) inhibitor or who have been pretreated with ruxolitinib.
Ruxolitinib: The JAK inhibitor ruxolitinib (Jakavi®) is indicated for the treatment of myeloproliferative neoplasms. These include myelofibrosis (MF) and polycythaemia vera (PV). Since May 2023, the active ingredient has also been approved in the form of a cream (Opzelura®) to support repigmentation in non-segmental vitiligo . Experimental in atopic dermatitis.
Upadacitinib and filgotinib primarily block the JAK1 kinase. Upadacitinib has been approved for rheumatoid arthritis since 03. 2021. Approval: Atopic dermatitis if local steroid therapy fails, these can continue to be used in parallel as required (from the age of 12) Psoriatic arthritis. The indication is for adult patients who have responded inadequately to one or more DMARDs or who cannot tolerate them. Upadacitinib can be used as monotherapy or in combination with methotrexate. Another indication is active ankylosing spondylitis and RA in adult patients who have responded inadequately to conventional therapy and ulcerative colitis.
Abrocitinib: selective JAK 1 inhibitor like upadacitinib Approval for the treatment of atopic dermatitis
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Pharmacodynamics (Effect)This section has been translated automatically.
The active ingredients have selective immunosuppressive, anti-inflammatory and antiproliferative properties. The effects are based on the inhibition of Janus kinases (JAK). These are intracellular enzymes that belong to the group of tyrosine kinases and transfer phosphate groups. They are involved in signal transduction from the cell membrane to the cell nucleus and have an influence on gene expression.
IndicationThis section has been translated automatically.
The best-known indication for Janus kinase inhibitors is currently rheumatoid arthritis. Other indications exist:
- Psoriatic arthritis
- Inflammatory bowel diseases, ulcerative colitis
- Myelofibrosis, polycythaemia vera
- Allergic dermatitis, atopic dermatitis (veterinary)
- Alopecia areata
Further approvals in the field of autoimmune diseases are expected.
Pregnancy/nursing periodThis section has been translated automatically.
The use of JAK inhibitors is not permitted according to the current state of knowledge.
Undesirable effectsThis section has been translated automatically.
The risk of side effects is similar to all JAK inhibitors and the biologics: first and foremost is the increased risk of infection. In contrast to the established biologics such as the TNF-alpha antagonists, an increased rate of varicella-zoster reactivations occurs under the therapy with Janus kinase inhibitors - especially when using higher dosages. In a recent meta-analysis of nearly 6,000 patients, the overall risk was 3.2 herpes zoster infections per 100 patient-years; the relative risks for the individual janus kinase inhibitors were approximately 2.0 for tofacitinib, 3.2 for baricitinib, and 3.0 for upadacitinib. Even if the exact mechanism of varicella-zoster reactivation is not yet known, interferon-α- and interferon-γ-mediated immune processes seem to play an important role in the control of the disease. Despite the often self-limiting course, therapeutic options for herpes zoster are limited. Even though many diseases remain uncomplicated, a proportion of affected individuals continue to experience distressing symptoms for a prolonged period of time, as well as an increase in risk towards myocardial infarction and stroke (Prechter F et al. 2019) .
Risk of thrombosis: For tofacitinib (Xeljanz), there is a warning for the higher dose of 2 x 10 mg/day. For the other JAK inhibitors, this risk seems to be less.
Prevention: Currently, there are several options for vaccination against varicella zoster virus. Vaccination with a live attenuated vaccine (Varilix® or Varivax®) from 11 months of age has been recommended by the RKI since 2004, and since 2009 there has been a recommendation for a second vaccination at 15-23 months of age. In 2016, the rate of fully vaccinated children was 78 % . Since 2006, a live vaccine, Zostavax®, has been approved for vaccination from the age of 50. This vaccine can reduce the rate of reactivation after initial infection and has been shown in randomised trials to be more than 50% effective in protecting against herpes reactivation and 67% effective in protecting against post-herpetic neuralgia (Prechter F et al. 2019).
InteractionsThis section has been translated automatically.
Many Janus kinase inhibitors are substrates of CYP450 isozymes and interactions with CYP inhibitors and inducers are possible. Immunosuppressants may increase the adverse effects.
PreparationsThis section has been translated automatically.
- Baricitinib - Olumiant®
- Fedratinib - Inrebic®
- Ruxolitinib - Jakavi®
- Tofacitinib - Xeljanz®
- Upadacitinib - Rinvoq®
- Abrocitinib - Cibinqo ®
- Oclacitinib - Apoquel® - veterinary drugs
Note(s)This section has been translated automatically.
As with all long-term therapies that impair the immune system, regular control tests must be carried out in the laboratory (blood count, lipid metabolism, liver, kidney) and any abnormalities must be clarified. Janus kinase inhibitors should be used with caution if there are far too few red blood cells (severe anaemia), as JAK inhibitors can intensify this effect.
LiteratureThis section has been translated automatically.
- Fleischmann R et al (2012) Placebo-controlled trial of tofacitinib monotherapy in rheumatoid arthritis. N Engl J Med 367:495-507.
- O'Shea JJ et al (2013) Janus kinase inhibitors in autoimmune diseases. Ann Rheum Dis 72 Suppl 2: ii111-115.
- Pavithran K et al (2012) Janus kinase inhibitors: jackpot or potluck? Oncol Rev 6: e13
- Prechter F et al. (2019) Janus kinase inhibitors: therapy with a downer: reactivation of herpes zoster. Dtsch Arztebl 116: A-1540 / B-1271 / C-1251.
- Triyangkulsri K et al. (2018) Role of janus kinase inhibitors in th treatment of alopecia areata. Drug Des Devel Ther 12: 2323-2335
- van Vollenhoven RF et al (2012) Tofacitinib or adalimumab versus placebo in rheumatoid arthritis. N Engl J Med 367:508-519.