JAK1 inhibition

Janus kinases 1 (JAK1) is an enzyme that regulates immune cell function and JAK1 inhibition can help prevent the immune system from hurting healthy cells. JAK inhibitors are transforming the treatment landscape for autoimmune diseases.

What are JAK1 inhibitors?

JAK1 inhibitors are therapies that are being investigated to treat inflammatory and autoimmune diseases by dampening the immune system and preventing it from attacking healthy cells. In healthy people, the immune system is the body’s defense against infection. In people with autoimmune diseases, the immune system can become too active and mistakenly attack healthy cells.

Now, NS Pharma is working to utilize the benefits of JAK1 inhibitors to develop a treatment for people with rare conditions like with eosinophilic granulomatosis with polyangiitis (EGPA).

How can JAK1 inhibition help people with EGPA?

JAK1 inhibition can lower eosinophil levels. In people with EGPA, this could reduce blood vessel inflammation, potentially halting further tissue damage and symptoms.

NS Pharma is developing a selective JAK1 inhibitor, NS-229, for the rare autoimmune disease EGPA. People with EGPA often have abnormally high numbers of eosinophils and highly activated lymphocytes, both of which are a type of white blood cell.

High eosinophil levels and activated lymphocytes cause inflammation of the small blood vessels, resulting in restricted blood flow. Symptoms vary depending on the organ(s) affected but frequently include shortness of breath, skin rashes, and nerve pain.

How is NS Pharma developing a JAK1 inhibitor?

Our scientists are investigating if a JAK1 inhibitor can suppress immune cell activation to reduce inflammation and lessen EGPA symptoms. A Phase 2, double-blind, randomized, placebo-controlled study to gauge the efficacy and safety of NS-229 in the treatment of EGPA is underway in the United States, Europe and Japan.

Sources

  1. Eosinophilic Granulomatosis with Polyangiitis – Vasculitis Foundation. Accessed on July 19, 2024.https://www.vasculitisfoundation.org/education/vasculitis-types/eosinophilic-granulomatosis-with-polyangiitis/
  2. Eosinophilic Granulomatosis with Polyangiitis (EGPA) – American Lung Association. Accessed on July 19, 2024. https://www.lung.org/lung-health-diseases/lung-disease-lookup/egpa
  3. Hu X, Li J, Fu M, Zhao X, Wang W. The JAK/STAT signaling pathway: from bench to clinic. Signal Transduct Target Ther. 2021 Nov 26;6(1):402. doi: 10.1038/s41392-021-00791-1
  4. Vaglio A, Buzio C, Zwerina J. Eosinophilic granulomatosis with polyangiitis (Churg-Strauss): state of the art. Allergy. 2013 Mar;68(3):261-73. doi: 10.1111/all.12088
  5. Kouro T, Takatsu K. IL-5- and eosinophil-mediated inflammation: from discovery to therapy. Int Immunol. 2009 Dec;21(12):1303-9. doi: 10.1093/intimm/dxp102