Skin Health Psoriasis Treatment What Are IL-17 Inhibitors? Interleukin (IL)-17 inhibitors treat psoriasis by reducing inflammation. By Christopher Bergland Christopher Bergland As a retired ultra-endurance triathlete turned medical writer, Chris brings the same passion and commitment to science-based journalism as he did to running, biking, and swimming extraordinary distances. Learn about our editorial process Published on December 08, 2022 Medically reviewed by Leah Ansell, MD Medically reviewed by Leah Ansell, MD LinkedIn Leah Ansell, MD, is board-certified in cosmetic and medical dermatology. She is an assistant professor at Columbia University and works in private practice in New York City. Learn about our Medical Expert Board Print Table of Contents View All Table of Contents How They Work What They Treat Types Benefits and Risks Frequently Asked Questions Interleukin (IL)-17A is a pro-inflammatory cytokine (proteins that serve as messengers between cells) that plays a role in skin disorders such as psoriasis (PsO) and autoimmune diseases like psoriatic arthritis (PsA). IL-17 inhibitors block this cytokine’s inflammatory pathways and are used to treat psoriasis and psoriatic arthritis. IL-17 inhibitors belong to a family of biologic drugs called monoclonal antibodies that target the interleukin-17A receptor. This article explains how IL-17 inhibitors work, what they treat, and weighs the benefits and risks of taking these immunosuppressive biologic medications. ipopba / Getty Images How IL-17 Inhibitors Work All of these IL-17 inhibitors work in a similar way; they target the IL-17A receptor, which blocks the inflammatory pathway of this cytokine. Blocking IL-17A's inflammatory pathway improves psoriasis symptoms and helps reduce inflammation caused by other autoimmune diseases. In addition to targeting IL-17A, researchers are also looking at how inhibitors work downstream to affect interleukin-23, which stimulates IL-17 production by activating Th17 cells. The IL-23/IL-17 axis is a key area of focus for targeted therapies used to treat chronic inflammatory diseases. What IL-17 Inhibitors Treat Healthy amounts of pro-inflammatory cytokines protect and heal tissue inflammation. However, too much IL-17 contributes to the development of psoriasis. Psoriasis is a chronic skin condition caused by excessive secretion of pro-inflammatory cytokines such as interleukin-17A. Although the exact cause of psoriatic arthritis is unknown, 85% of people with psoriatic arthritis also have psoriasis.Both of these inflammatory diseases are treated with IL-17 inhibitors, which tame pro-inflammatory cytokines. Cosentyx (Secukinumab), Taltz (Ixekizumab), and Siliq (Brodalumab) are all IL-17-inhibiting psoriasis medications approved by the FDA to treat psoriasis and psoriatic arthritis. IL-17 inhibitors are also used to treat ankylosing spondylitis (AS), which is a type of inflammatory arthritis that primarily affects the spine. Types of IL-17 Inhibitors IL-17 inhibitors are a type of drug called "injectables" that are self-administered by subcutaneous injection applied with a needle under the skin. All three IL-17 inhibitors follow a similar dosing schedule of once a week during the first month, followed by once-monthly dosing for maintenance after the first five weeks. Cosentyx (Secukinumab), Taltz (Ixekizumab), and Siliq (Brodalumab) are similar types of drugs, but they each have slightly different dosing. Be sure to ask your pharmacist or a healthcare provider about the specific dosing schedule for the type of IL-17 inhibitor you're prescribed. These IL-17 Inhibitors Are FDA Approved Three IL-17 inhibitors—Cosentyx (secukinumab), Taltz (ixekizumab), and Siliq (brodalumab)—are FDA-approved for the treatment of plaque psoriasis and psoriatic arthritis. Benefits and Risks IL-17 inhibitors are one of the most effective biologic medications for the treatment of moderate-to-severe plaque psoriasis. In 2020, a meta-analysis of the cumulative clinical benefits of IL-17 inhibitors for the treatment of psoriasis over 16 weeks found that these biologics work much better than other medications. Numerous studies have established that IL-17 inhibitors are generally well-tolerated, safe, and provide significant benefits for people with psoriasis, psoriatic arthritis, and ankylosing spondylitis. However, these biologic medications are not without risks. Most notably, IL-17 inhibitors are immunosuppressants. They tone down the immune system, which increases the risk of serious infections. Immunosuppressive therapies also weaken the immune system's ability to detect and destroy cancer cells or fight the infections that cause cancer. Because of the immunosuppressive effects of IL-17 inhibitors, it's important to speak with a healthcare provider about what precautions you can take (e.g., getting vaccines before starting treatment) to minimize the risks associated with these biologics. Summary IL-17 inhibitors block the inflammatory pathway of interleukin-17A. These biologic medications are an extremely effective FDA-approved treatment option for people with psoriasis and psoriatic arthritis. These drugs, which are self-administered via subcutaneous injection, are also approved for the treatment of ankylosing spondylitis and axial spondyloarthritis. Although IL-17 inhibitors have significant benefits, they also have immunosuppressive effects, which can increase the risk of serious infections and other adverse reactions. A Word From Verywell Since IL-17 inhibitors were first approved by the FDA in 2015, they've radically improved quality of life for people living with psoriasis and psoriatic arthritis. These monoclonal antibodies are a game-changer. That said, these biologics are immunosuppressive and tamp down the immune system, which increases your risk of infection and certain types of cancer. When taking IL-17 inhibitors, always stay in close communication with a healthcare provider to monitor and fine-tune your treatment plan to optimize benefits while minimizing risks. Frequently Asked Questions What's the difference between Cosentyx, Taltz, and Siliq? Cosentyx (secukinumab), Taltz (ixekizumab), and Siliq (brodalumab) are three very similar IL-17 inhibitors that work by blocking the inflammatory pathway of interleukin-17A. These biologic drugs are all FDA-approved for the treatment of psoriasis and psoriatic arthritis. Cosentyx and Taltz are also used to treat a form of inflammatory arthritis called ankylosing spondylitis. Learn More: An Overview of Biologics for Treating Psoriatic Disease What causes psoriasis and how do you treat it? Psoriasis (PsO) and psoriatic arthritis (PsA) are chronic autoimmune disorders. Researchers believe that PsO and PsA are caused by an overactive immune system, which triggers the release of too many pro-inflammatory cytokines like interleukin-17A. IL-17 inhibitors target IL-17A's inflammatory pathways and are used to treat psoriatic disease. Learn More: How Psoriasis Is Treated Do IL-17 inhibitors suppress the immune system? IL-17 inhibitors are immunosuppressive therapies that suppress the immune system's ability to make excessive pro-inflammatory cytokines. Although tamping down the immune system with these medications reduces inflammation and dramatically helps people with psoriatic disease, immunosuppression increases the risk of infection and can have other adverse effects. Learn More: What to Know About Immunosuppressive Therapies 15 Sources Verywell Health uses only high-quality sources, including peer-reviewed studies, to support the facts within our articles. Read our editorial process to learn more about how we fact-check and keep our content accurate, reliable, and trustworthy. Mosca M, Hong J, Hadeler E, Hakimi M, Liao W, Bhutani T. The role of IL-17 cytokines in psoriasis. ITT. 2021;Volume 10:409-418. doi:10.2147/ITT.S240891 Lonnberg, Skov L, Zachariae C. Targeting of interleukin-17 in the treatment of psoriasis. CCID. Published online September 2014:251. doi:10.2147/CCID.S67534 Girolomoni G, Mrowietz U, Paul C. Psoriasis: Rationale for targeting interleukin-17: IL-17 in psoriasis. British Journal of Dermatology. 2012;167(4):717-724. doi:10.1111/j.1365-2133.2012.11099.x Iwakura Y. The IL-23/IL-17 axis in inflammation. Journal of Clinical Investigation. 2006;116(5):1218-1222. doi:10.1172/JCI28508 Bianchi E, Vecellio M, Rogge L. Editorial: role of the IL-23/IL-17 pathway in chronic immune-mediated inflammatory diseases: Mechanisms and targeted therapies. Front Immunol. 2021;12:770275. doi:10.3389/fimmu.2021.770275 Wasilewska A, Winiarska M, Olszewska M, Rudnicka L. Interleukin-17 inhibitors. A new era in treatment of psoriasis and other skin diseases. pdia. 2016;4:247-252. doi:10.5114/ada.2016.61599 Chiricozzi A, Suárez‐Fariñas M, Fuentes‐Duculan J, et al. Increased expression of interleukin‐17 pathway genes in nonlesional skin of moderate‐to‐severe psoriasis vulgaris. Br J Dermatol. 2016;174(1):136-145. doi:10.1111/bjd.14034 Merola JF, Espinoza LR, Fleischmann R. Distinguishing rheumatoid arthritis from psoriatic arthritis. RMD Open. 2018;4(2):e000656. doi:10.1136/rmdopen-2018-000656 Dermatology Times. Psoriasis Updates: Comparing IL-23 and IL-17 Inhibitors, TNF Blockers. Yin Y, Wang M, Liu M, et al. Efficacy and safety of IL-17 inhibitors for the treatment of ankylosing spondylitis: a systematic review and meta-analysis. Arthritis Res Ther. 2020;22(1):111. doi:10.1186/s13075-020-02208-w Hanley TL, Yiu ZZ. Role of IL-17 in plaque psoriasis: therapeutic potential of ixekizumab. Ther Clin Risk Manag. 2017;13:315-323. doi:10.2147/TCRM.S111107 Warren RB, Gooderham M, Burge R, et al. Comparison of cumulative clinical benefits of biologics for the treatment of psoriasis over 16 weeks: Results from a network meta-analysis. Journal of the American Academy of Dermatology. 2020;82(5):1138-1149. doi: McGonagle DG, McInnes IB, Kirkham BW, Sherlock J, Moots R. The role of IL-17A in axial spondyloarthritis and psoriatic arthritis: recent advances and controversies. Ann Rheum Dis. 2019;78(9):1167-1178. doi:10.1136/annrheumdis-2019-215356 NIH: National Cancer Institute. Immunosuppression. Papp KA, Haraoui B, Kumar D, et al. Vaccination guidelines for patients with immune-mediated disorders on immunosuppressive therapies. J Cutan Med Surg. 2019;23(1):50-74. doi:10.1177/1203475418811335 By Christopher Bergland Christopher Bergland is a retired ultra-endurance athlete turned medical writer and science reporter. See Our Editorial Process Meet Our Medical Expert Board Share Feedback Was this page helpful? Thanks for your feedback! What is your feedback? Other Helpful Report an Error Submit