Emmi Giacomo, Silvestri Elena, Squatrito Danilo, D'Elios Mario Milco, Ciucciarelli Lucia, Prisco Domenico, Emmi Lorenzo
Department of Experimental and Clinical Medicine, University of Florence, L.go G. Brambilla 3, 50134, Florence, Italy,
Intern Emerg Med. 2014 Apr;9(3):257-65. doi: 10.1007/s11739-013-1036-5. Epub 2014 Jan 12.
Behçet syndrome is a systemic inflammatory disorder characterized by multiorgan involvement such as oral and genital ulcers, uveitis, skin lesions as well as by less frequent, but often more severe, central nervous system and vascular manifestations. The pathogenetic mechanisms are still incompletely known; however the interaction between a specific genetic background and environmental or infectious factors certainly contributes to the immune dysregulation that characterizes this disease. The discovery of new immunological pathways in Behçet syndrome pathogenesis may help us to set up new treatments. In this review, we will focus our attention on the possible mechanisms underlying Behçet syndrome pathogenesis and their potential role as novel therapeutic targets.
白塞病是一种全身性炎症性疾病,其特征为多器官受累,如口腔和生殖器溃疡、葡萄膜炎、皮肤病变,以及较少见但往往更严重的中枢神经系统和血管表现。其发病机制仍不完全清楚;然而,特定遗传背景与环境或感染因素之间的相互作用肯定会导致该疾病所特有的免疫失调。白塞病发病机制中新免疫途径的发现可能有助于我们建立新的治疗方法。在这篇综述中,我们将把注意力集中在白塞病发病机制的潜在机制及其作为新型治疗靶点的潜在作用上。