2014DOAJ (DOAJ: Directory of Open Access Journals)Open access

Profile of ustekinumab and its potential in patients with moderate-to-severe Crohn's disease

Anne Tuskey, Behm BW

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Abstract

Anne Tuskey, Brian W Behm Division of Gastroenterology and Hepatology, University of Virginia School of Medicine, Charlottesville, VA, USA Abstract: The advent of anti-tumor necrosis factor (TNF)-α therapy has been a major advance in the medical management of Crohn's disease (CD). However, a significant proportion of patients with CD do not respond adequately to treatment with these agents. Primary and secondary nonresponse to anti-TNFα therapy represents a common clinical challenge, and highlights the need for the development of additional medication options for CD. The proinflammatory cytokines interleukin (IL)-12 and IL-23 are thought to play a key role in the pathogenesis of CD, and serve as a potential target for additional biologic therapies. Monoclonal antibodies targeting IL-12/23 have shown efficacy in animal models of colitis, and are currently being studied in Phase III clinical trials of CD. This review focuses on ustekinumab, a fully human immunoglobulin G1 monoclonal antibody, which blocks activity of IL-12 and IL-23 through binding the p40 subunit, and describes the current efficacy and safety data for ustekinumab in patients with CD. Keywords: Crohn's disease, ustekinumab, clinical trials, inflammatory bowel disease

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What this paper is about

Anne Tuskey, Brian W Behm Division of Gastroenterology and Hepatology, University of Virginia School of Medicine, Charlottesville, VA, USA Abstract: The advent of anti-tumor necrosis factor (TNF)-α therapy has been a major advance in the medical management of Crohn's disease (CD). However, a significant proportion of patients with CD do not respond adequately to treatment with these agents. Primary and secondary nonresponse to anti-TNFα therapy represents a common clinical challenge, and highlights the need for the development of additional medication options for CD. The proinflammatory cytokines interleukin (IL)-12 and IL-23 are thought to play a key role in the pathogenesis of CD, and serve as a potential target for additional biologic therapies. Monoclonal antibodies targeting IL-12/23 have shown efficacy in animal models of colitis, and are currently being studied in Phase III clinical trials of CD. This review focuses on ustekinumab, a fully human immunoglobulin G1 monoclonal antibody, which blocks activity of IL-12 and IL-23 through binding the p40 subunit, and describes the current efficacy and safety data for ustekinumab in patients with CD. Keywords: Crohn's disease, ustekinumab, clinical trials, inflammatory bowel disease

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Available abstract

Anne Tuskey, Brian W Behm Division of Gastroenterology and Hepatology, University of Virginia School of Medicine, Charlottesville, VA, USA Abstract: The advent of anti-tumor necrosis factor (TNF)-α therapy has been a major advance in the medical management of Crohn's disease (CD). However, a significant proportion of patients with CD do not respond adequately to treatment with these agents. Primary and secondary nonresponse to anti-TNFα therapy represents a common clinical challenge, and highlights the need for the development of additional medication options for CD. The proinflammatory cytokines interleukin (IL)-12 and IL-23 are thought to play a key role in the pathogenesis of CD, and serve as a potential target for additional biologic therapies. Monoclonal antibodies targeting IL-12/23 have shown efficacy in animal models of colitis, and are currently being studied in Phase III clinical trials of CD. This review focuses on ustekinumab, a fully human immunoglobulin G1 monoclonal antibody, which blocks activity of IL-12 and IL-23 through binding the p40 subunit, and describes the current efficacy and safety data for ustekinumab in patients with CD. Keywords: Crohn's disease, ustekinumab, clinical trials, inflammatory bowel disease

Key concepts: Ustekinumab, Crohn's disease, Medicine, Crohn disease, Internal medicine, Disease, Gastroenterology, Adalimumab

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