Ustekinumab in the Treatment of Inflammatory Bowel Diseases: Evolving Paradigms

Author:

Mocci Giammarco1,Tursi Antonio23ORCID,Onidi Francesca Maria1,Usai-Satta Paolo1ORCID,Pes Giovanni Mario4ORCID,Dore Maria Pina45ORCID

Affiliation:

1. Division of Gastroenterology, “Brotzu” Hospital, 09124 Cagliari, Italy

2. Territorial Gastroenterology Service, ASL BAT, 76123 Andria, Italy

3. Department of Medical and Surgical Sciences, School of Medicine, Catholic University, 00168 Rome, Italy

4. Department of Medicine, Surgery and Pharmacy, University of Sassari, 07100 Sassari, Italy

5. Baylor College of Medicine, One Baylor Plaza Blvd., Houston, TX 77030, USA

Abstract

Inflammatory bowel diseases, comprising Crohn’s disease (CD) and ulcerative colitis (UC), are chronic, relapsing, and remitting immune-mediated inflammatory diseases affecting the gastrointestinal tract. Ustekinumab (UST) is a monoclonal antibody that blocks the p40 subunit of the anti-interleukin (IL) 12/23. Pivotal trials (CERTIFI and UNITI-IM for CD, UNIFI for UC) established the efficacy of UST for the induction and maintenance of remission in both CD and UC, with the most favorable results in naïve patients to biologics. In recent years, a wealth of ‘real-world’ data has emerged supporting positive clinical, endoscopic, and histological outcomes in patients treated with UST, as well as reassuring safety data. More recently, the results of the first head-to-head trials of UST and tumor necrosis factor (TNF) antagonists were reported. Moreover, a number of studies exploring the role of UST in specific clinical settings, such as perianal CD, postoperative complications and recurrence, extraintestinal manifestations, chronic antibiotic-refractory pouchitis, and pregnancy, were reported. This review explores the results reported to date on UST, including those from pivotal trials, real-world data, and emerging studies regarding therapeutic drug monitoring and immunogenicity. The safety profile of UST was also reviewed.

Publisher

MDPI AG

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