New pharmacotherapy options for noninfectious posterior uveitis

被引:14
|
作者
Pleyer, Uwe [1 ]
Stuebiger, Nicole [1 ,2 ]
机构
[1] Humboldt Univ, Charite Univ Med Berlin, Dept Ophthalmol, D-13353 Berlin, Germany
[2] Humboldt Univ, Univ Eye Clin Charite, D-13353 Berlin, Germany
关键词
autoimmunity; biological; corticosteroid; cytokine; kinase inhibitor; small-molecular-weight inhibitor; uveitis; FLUOCINOLONE ACETONIDE IMPLANT; JUVENILE IDIOPATHIC ARTHRITIS; INTRAVENOUS IMMUNOGLOBULIN THERAPY; LONG-TERM TREATMENT; BEHCETS-DISEASE; RETINAL VASCULITIS; INTRAVITREAL TRIAMCINOLONE; INTRAOCULAR METHOTREXATE; OCULAR INFLAMMATION; REFRACTORY UVEITIS;
D O I
10.1517/14712598.2014.956074
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Introduction: Noninfectious posterior uveitis is a leading cause of visual impairment. Although conventional immunosuppressive agents have been successfully used, these are nonspecific and their long-term use may induce significant adverse effects. The purpose of this article is to identify recent advances and future therapeutic options in noninfectious posterior uveitis. Areas covered: A MEDLINE database search was conducted through May 2014 using the terms: uveitis, treatment, intravitreal and corticosteroid, biological. To provide ongoing and future perspectives in treatment options, also clinical trials as registered at ClinicalTrials.gov were included. Expert opinion: For individuals who do not respond to conventional immunotherapy, two major lines of treatments can be identified as focus in recent years: i) the intraocular application of anti-inflammatory drugs and ii) the introduction of new agents, for example, biologicals and small-molecule inhibitors. Whereas intravitreal treatments have the beauty of avoiding systemic side effects, new agents are gaining increased importance because of their highly targeted molecular effects. Even when current treatment strategies are still hampered by the paucity of randomized controlled trials, promising progress and continuous efforts are undertaken to close this gap. Still, a critical evaluation of new agents has to be made because 'new' agents are almost exclusively based on experience in other autoimmune disorders.
引用
收藏
页码:1783 / 1799
页数:17
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