| Literature DB >> 25151975 |
Luca Cantarini1, Giuseppe Lopalco2, Francesco Caso3, Luisa Costa4, Florenzo Iannone2, Giovanni Lapadula2, Maria Grazia Anelli2, Rossella Franceschini5, Cristina Menicacci5, Mauro Galeazzi6, Carlo Selmi7, Donato Rigante8.
Abstract
Behçet's disease (BD) is a multi-systemic disorder of unknown etiology characterized by relapsing oral-genital ulcers, uveitis, and involvement of the articular, gastrointestinal, neurologic, and vascular systems. Although the primum movens of this condition remains unknown, a tangled plot combining autoimmune and autoinflammatory pathways has been hypothesized to explain its start and recurrence. In-depth analysis of BD pathogenetic mechanisms, involving dysfunction of multiple proinflammatory molecules, has opened new modalities of treatment: different agents targeting interleukin-1 have been studied in recent years to manage the most difficult and multi-resistant cases of BD. Growing experience with anakinra, canakinumab and gevokizumab is discussed in this review, highlighting the relative efficacy of each drug upon the protean BD clinical manifestations. Safety and tolerability of interleukin-1 antagonists in different doses have been confirmed by numerous observational studies on both large and small cohorts of patients with BD. In particular, the potential for Mycobacterium tuberculosis reactivation and tuberculosis development appears to be significantly lower with interleukin-1 blockers compared to tumor necrosis factor-α inhibitors, thus increasing the beneficial profile of this approach.Entities:
Keywords: Anakinra; Behçet's disease; Canakinumab; Gevokizumab; Interleukin-1; Tuberculosis
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Year: 2014 PMID: 25151975 DOI: 10.1016/j.autrev.2014.08.008
Source DB: PubMed Journal: Autoimmun Rev ISSN: 1568-9972 Impact factor: 9.754