Immunomodulators
Immunomodulators
Immunomodulators
Information included in this Introduction to IBD Medication Classes is for educational purposes only and is intended for US-based healthcare providers (HCPs).
This information does not represent medical advice or endorse any specific product. It should not be the basis for clinical diagnoses or treatment decisions.
Use this information in conjunction with a clinical assessment and independent research from other relevant sources.
This information was last updated 1/2026.
Medication Class Introduction
Immunomodulator medications represent a class of therapies introduced in the 1960s to manage inflammatory bowel disease (IBD).1,2 These drugs target the immune system, aiming to modulate the dysregulated immune response that drives intestinal inflammation in IBD.3–6 Their therapeutic effect generally involves suppressing immune activity by limiting the proliferation and survival of immune cells involved in driving inflammation.2,5,7
IBD Treatment Landscape8–18
JAK=Janus kinase; S1P=sphingosine-1-phosphate; TNF=tumor necrosis factor.
Role in IBD Pathogenesis
IBD is characterized by immune cell dysregulation, which may impair the clearance of activated cells and promote their continued proliferation and survival.3–5,19 This dysregulation can result in elevated pro-inflammatory cytokine production, ultimately resulting in chronic intestinal inflammation.4,5,19

Mechanism of Action in IBD
Immunomodulators can exert their effects by inhibiting immune cell proliferation and survival, though the specific mechanisms vary by agent.1,2,5,6,11,20,21 Some immunomodulator mechanisms of action inhibit key enzymatic processes involved in purine synthesis, disrupting DNA replication and cell division in lymphocytes, while others alter intracellular signaling pathways, leading to the induction of immune cell apoptosis (programmed cell death).1,2,5–7,11 Additionally, immunomodulatory therapy can suppress production of pro-inflammatory cytokines, further reducing signaling that drives chronic inflammation.2,5,6
DNA=deoxyribonucleic acid.
Resources
Current IBD Treatment Guidelines
Guidelines for managing IBD are available from the American College of Gastroenterology (ACG) and the American Gastroenterological Association (AGA). You can access them through the following links:
- ACG Clinical Guideline: Management of Crohn’s Disease in Adults
- ACG Clinical Guideline Update: Ulcerative Colitis in Adults
- AGA Living Clinical Practice Guideline on the Pharmacologic Management of Moderate-to-Severe Crohn’s Disease
- AGA Clinical Practice Guidelines on the Management of Mild-to-Moderate Ulcerative Colitis
- AGA Living Clinical Practice Guideline on Pharmacological Management of Moderate-to-Severe Ulcerative Colitis
Resources to Help Explain Medication Options for IBD to Patients
The Crohn’s & Colitis Foundation resources below may help you explain medication options, including the mechanism of action of IBD medication classes and how they are designed to work in the body, to your patients with IBD.
Resources to Help Understand Medical Management of IBD From UpToDate®
The UpToDate® resources below may help you understand medical management of IBD in adults including but not limited to disease activity, severity, and risk, as well as medication options for induction and maintenance.
- Medical management of mild Crohn’s disease
- Medical management of moderate to severe Crohn’s disease
- Medical management of mild to moderate ulcerative colitis
- Medical management of moderate to severe ulcerative colitis
For More Information on IBD Medications
To learn more about the medications commonly used to treat IBD—including potential side effects and safety considerations—please refer to the following resource:
Links to third-party websites are provided as resources and not intended to be an endorsement. Takeda is not responsible for their content.
- Imbrizi M, Magro F, Coy CSR. Pharmaceuticals (Basel). 2023;16(9):1272.
- Venner JM, Bernstein CN. Gastroenterol Rep (Oxf). 2022;10:goac061.
- Sanchez-Munoz, Dominguez-Lopez A, Yamamoto-Furusho J. World J Gastroenterol. 2008;14(27):4280-4288.
- Neurath MF. Nat Rev Immunol. 2024;24(8):559-576.
- Cai Z, Wang S, Li J. Front Med (Lausanne). 2021;8:765474.
- Thomas A, Lodhia N. J Am Fam Med. 2014;27(3):411-420.
- Cornish JS, Wirthgen E, Däbritz J. Front Med (Lausanne). 2020;7:8.
- Lichtenstein GR, Loftus EV, Afzali A, et al. Am J Gastroenterol. 2025;120(6):1225-1264.
- Murray A, Nguyen TM, Parker CE, Feagan BG, MacDonald JK. Cochrane Database Syst Rev. 2020;8(8):CD000544.
- Dorrington AM, Selinger CP, Parkes GC, Smith M, Pollok RC, Raine T. J Crohns Colitis. 2020;14(9):1316-1329.
- de Boer NKH, Peyrin-Biroulet L, Jharap B, et al. J Crohns Colitis. 2018;12(5):610-620.
- Actis GC, Pellicano R, Fagoonee S, Ribaldone DG. J Clin Med. 2019;8(11):1970.
- Santiago P, Braga-Neto MB, Loftus EV Jr. Gastroenterol Hepatol (N Y). 2022;18(8):453-465.
- Pérez-Jeldres T, Tyler CJ, Boyer JD, et al. Front Pharmacol. 2019;10:212.
- Fudman DI, McConnell RA, Ha C, Singh S. Clin Gastroenterol Hepatol. 2025;23(3):454-469.
- Moschen AR, Tilg H, Raine T. Nat Rev Gastroenterol Hepatol. 2019;16(3):185-196.
- Choden T, Cohen NA, Rubin DT. Gastroenterol Hepatol (N Y). 2022;18(5):265-271.
- Martinez-Molina C, González-Suárez B. J Clin Med. 2025;14(11):3890.
- Vebr M, Pomahačová R, Sýkora J, Schwarz J. Biomedicines. 2023;11(12):3229.
- Mantzaris GJ. Curr Treat Options Gastroenterol. 2017;15(1):84-104.
- AlAmeel T, Al Sulais E, Raine T. Saudi J Gastroenterol. 2022;28(4):250-260.
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