Cyclosporin A and iloprost treatment of systemic sclerosis: clinical results and interleukin-6 serum changes after 12 months of therapy

被引:74
作者
Filaci, G
Cutolo, M
Scudeletti, M
Castagneto, C
Derchi, L
Gianrossi, R
Ropolo, F
Zentilin, P
Sulli, A
Murdaca, G
Ghio, M
Indiveri, F
Puppo, F
机构
[1] Univ Genoa, Dipartimento Med Interna, Div Internal Med, I-16132 Genoa, Italy
[2] Univ Genoa, Dept Internal Med, Div Rheumatol, I-16132 Genoa, Italy
[3] Univ Genoa, Inst Radiol, I-16132 Genoa, Italy
[4] Osped San Martino Genova, Div Pneumol, Genoa, Italy
[5] Univ Genoa, Dept Internal Med, Div Gastroenterol, Genoa, Italy
关键词
systemic sclerosis; cyclosporin A; iloprost; interleukin; 6;
D O I
10.1093/rheumatology/38.10.992
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives. The main aim was to analyse the long-term therapeutic effects on systemic sclerosis (SSc) patients of treatment with either (i) iloprost alone or (ii) low-dose oral cyclosporin A (CyA) associated with iloprost. A secondary aim was to analyse interleukin-6 (IL-6) serum levels in SSc patients before and after 1 yr of treatment. Methods. A clinical trial was performed in which 20 consecutive SSc patients were alternately randomized into two homogeneous groups receiving either monthly i.v. iloprost (1 ng/kg/min in 6 h i.v. infusion, for 5 consecutive days, 1 week per month) (Group I) or low-dose CyA (2.5 mg/kg/day) associated with iloprost administration (Group II). IL-6 concentrations were evaluated by ELISA in the sera of each patient before and after 1 yr of therapy and in 20 healthy subjects. Results. After 1 yr of therapy, a significant improvement of skin (P = 0.008), microvascular (P = 0.004) and oesophageal (P = 0.05) morphological and functional parameters was observed only in Group II patients. Furthermore, after 1 yr of treatment, a significant reduction (P = 0.007) of IL-6 serum concentration was observed only in Group II patients. Conclusions. Collectively, our data suggest that the combination of low-dose CyA with iloprost administration may be of clinical utility in SSc and that a mechanism of action of CyA in SSc may include the decrease in IL-6 production.
引用
收藏
页码:992 / 996
页数:5
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