Topical Fk506 in inflammatory corneal and conjunctival diseases - A pilot study

被引:37
作者
Reinhard, T [1 ]
Reis, A [1 ]
Mayweg, S [1 ]
Oberhuber, H [1 ]
Mathis, G [1 ]
Sundmacher, R [1 ]
机构
[1] Univ Dusseldorf, Augenklin, D-50225 Dusseldorf, Germany
关键词
cyclosporin A; Fk506; interleukin; 2; keratitis;
D O I
10.1055/s-2002-26727
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Background: Topical corticosteroids are the only effective measure in serious inflammatory corneal and conjunctival diseases. Although results obtained with topical cyclosporin A are encuraging it is not effective in all patients. The mode of action of Fk506 is similar to that of cyclosporin A, i.e. it exerts an inhibitory effect on transcription of interleukin 2 in T lymphocytes. The immunosuppressive potential of Fk506, however, is much larger. Furthermore, it penetrates more easily into cornea and conjunctiva. To find out whether the theoretical advantages of topical Fk506 can be translated into clinical practice, a selected group of patients refractory to conventional therapy was treated in this pilot study. Patients and methods: Fk506 0.06% was administered initially three times daily in 15 patients with atopic blepharokeratoconjunctivitis, Mooren's ulcer, ocular pemphigoid, Thygeson's superficial punctate keratitis, nummular adenoviral keratitis, graft-versus-host reaction of the conjunctiva and steroid response glaucoma after penetrating keratoplasty. Results: Within a follow-up of 26 15 weeks improvement was recorded in 5/15 patients and stabilization in 5/15 patients. In two patients progression of the disease was noted (one patient with progression of ocular pemphigoid, another patient with suspected automutilation). Premature withdrawal the drug was judged to be necessary in two patients with ocular surface disorders and in one patient with non-compliance. Conclusions: Topical Fk506 seems to be a promising new immunosuppressive drug for patients with atopic blepharokeratoconjunctivitis, Thygeson's superficial punctate keratitis and nummular adenoviral keratitis. Exact efficacy in these and other corneal and conjunctival inflammatory diseases has to be determined in randomised clinical studies. Before these studies may start the risk of side-effects must be reduced via an improvement of the drops.
引用
收藏
页码:125 / 131
页数:7
相关论文
共 29 条
[1]   CYCLOSPORINE EYEDROPS FOR THE TREATMENT OF SEVERE VERNAL KERATOCONJUNCTIVITIS [J].
BENEZRA, D ;
PEER, J ;
BRODSKY, M ;
COHEN, E .
AMERICAN JOURNAL OF OPHTHALMOLOGY, 1986, 101 (03) :278-282
[2]  
BLEIK JH, 1991, OPHTHALMOLOGY, V98, P1679
[3]  
CELLI S, 1993, TRANSPLANT P, V25, P647
[4]   IDENTIFICATION OF CALCINEURIN AS A KEY SIGNALING ENZYME IN LYMPHOCYTE-T ACTIVATION [J].
CLIPSTONE, NA ;
CRABTREE, GR .
NATURE, 1992, 357 (6380) :695-697
[5]  
GEGGEL HS, 1994, CORNEA, V13, P543
[6]  
Hikita N, 1997, INVEST OPHTH VIS SCI, V38, P901
[7]   TOPICAL CYCLOSPORINE-A IN THE TREATMENT OF ANTERIOR SEGMENT INFLAMMATORY DISEASE [J].
HOLLAND, EJ ;
OLSEN, TW ;
KETCHAM, JM ;
FLORINE, C ;
KRACHMER, JH ;
PURCELL, JJ ;
LAM, S ;
TESSLER, HH ;
SUGAR, J .
CORNEA, 1993, 12 (05) :413-419
[8]   FK-506, A NOVEL IMMUNOSUPPRESSANT ISOLATED FROM A STREPTOMYCES .1. FERMENTATION, ISOLATION, AND PHYSICOCHEMICAL AND BIOLOGICAL CHARACTERISTICS [J].
KINO, T ;
HATANAKA, H ;
HASHIMOTO, M ;
NISHIYAMA, M ;
GOTO, T ;
OKUHARA, M ;
KOHSAKA, M ;
AOKI, H ;
IMANAKA, H .
JOURNAL OF ANTIBIOTICS, 1987, 40 (09) :1249-1255
[9]  
Lauerma AI, 1997, SKIN PHARMACOL, V10, P230
[10]  
LYONS CJ, 1990, OPHTHALMOLOGY, V97, P729