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Abstract
<p class="first" id="d984666e82">Inflammatory bowel disease (IBD) is a chronic inflammatory
disease of the gastrointestinal
tract. Cytokine-targeted therapies have transformed the treatment of IBD, providing
control of symptoms and longer relapse-free periods. However, many patients fail to
respond, highlighting the need for therapies tailored to the underlying cell and molecular
disease drivers. Here we discuss the progression of IBD from the perspective of remodeling
of cytokine networks. We place well-established and under-studied cytokine modules
in the context of cellular interactions, their dynamic regulation in early and late
stages of disease (i.e., fibrosis), and their current and potential use in the clinic.
Examining how particular cytokine networks drive distinct features and phases of IBD
will shed light on the etiology of IBD and provide a basis for more effective treatments.
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