Bertelmann Eckart, Pleyer Uwe
Augenklinik Charité - Universitätsmedizin Berlin, Campus Virchow Klinikum, Berlin, Deutschland.
Ophthalmologica. 2004 Nov-Dec;218(6):359-67. doi: 10.1159/000080937.
Topical corticosteroids, although effective in the treatment of ocular immune-mediated diseases, are well known for their ocular side-effects. Not surprisingly, a variety of alternative immunomodulatory agents have been tested for topical use including cyclosporin A (CsA), mycophenolate mofetil (MMF), tacrolimus (FK506), rapamycin (sirolimus) and leflunomide. Local application bears the possibility to avoid the severe side-effects of systemic therapy. The effect of topical therapy is naturally restricted to local immune response mechanisms, such as antigen presentation by Langerhans and dendritic cells. Moreover, many immunomodulatory agents (e.g. CsA) are lipophilic and thus have low water solubility and penetrate insufficiently intra-ocularly, often being stored in the lipophilic corneal epithelial barrier. Therefore, the therapeutical success is limited for intra-ocular immune-mediated diseases like anterior uveitis. However, a multitude of strategies have been introduced to circumvent these problems including complexing substances such as cyclodextrins (CDs) and liposomes. In the prevention and treatment of transplant rejection after keratoplasty, many attempts to introduce topical immunomodulatory therapy have failed; on the other hand, further therapeutic options not primarily expected are being evaluated today such as treatment of severe keratoconjunctivitis sicca. In our own studies, we investigated the pharmacokinetics of topical treatment with different agents including MMF and evaluated the efficacy of topical treatment in animal models for uveitis and keratoplasty. Taken together, topical immunomodulatory therapy will not replace systemic therapy but further treatment options can be expected.
局部用皮质类固醇虽然在治疗眼部免疫介导疾病方面有效,但因其眼部副作用而广为人知。毫不奇怪,人们已经测试了多种用于局部使用的替代免疫调节药物,包括环孢素A(CsA)、霉酚酸酯(MMF)、他克莫司(FK506)、雷帕霉素(西罗莫司)和来氟米特。局部应用有可能避免全身治疗的严重副作用。局部治疗的效果自然局限于局部免疫反应机制,如朗格汉斯细胞和树突状细胞的抗原呈递。此外,许多免疫调节药物(如CsA)具有亲脂性,因此水溶性低,眼内穿透力不足,常储存在亲脂性角膜上皮屏障中。因此,对于前葡萄膜炎等眼内免疫介导疾病,治疗成功率有限。然而,已经引入了多种策略来规避这些问题,包括使用环糊精(CDs)和脂质体等复合物质。在角膜移植术后移植排斥反应 的预防和治疗中,许多引入局部免疫调节治疗的尝试都失败了;另一方面,如今正在评估一些并非最初预期的进一步治疗选择,如重度干眼症的治疗。在我们自己的研究中,我们研究了包括MMF在内的不同药物局部治疗的药代动力学,并评估了局部治疗在葡萄膜炎和角膜移植动物模型中的疗效。综上所述,局部免疫调节治疗不会取代全身治疗,但有望出现更多的治疗选择。