Upregulation of Myxovirus-resistance Protein A: A Possible Marker of Type I Interferon Induction in Systemic Sclerosis

被引:27
作者
Airo, Paolo [1 ,2 ]
Ghidini, Claudia [3 ]
Zanotti, Cinzia [3 ]
Scarsi, Mirko [1 ,2 ]
Cattaneo, Roberto [1 ,2 ]
Caimi, Luigi [3 ]
Imberti, Luisa [3 ]
机构
[1] Spedali Civil Brescia, Rheumatol & Clin Immunol Serv, I-25123 Brescia, Italy
[2] Univ Brescia, Brescia, Italy
[3] Spedali Civil Brescia, Lab Biotecnol, Diagnost Dept, I-25123 Brescia, Italy
关键词
SYSTEMIC SCLEROSIS; TYPE I INTERFERON; MYXOVIRUS-RESISTANCE PROTEIN A; INTERFERON RECEPTOR;
D O I
10.3899/jrheum.080418
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. To examine whether myxovirus-resistance protein A (MxA) mRNA expression, commonly considered a reliable marker of Type I interferon (IFN) bioactivity, is modified in patients with systemic sclerosis (SSc); if it is associated to specific clinical features; and if its modulation is accompanied by modulation of mRNA for the Type I IFN receptor (IFNAR). Methods. Quantification of mRNA for MxA and the subunit IFNAR I and isoforms of IFNAR2 was performed by real-time polymerase chain reaction in 50 patients with SSc. Results were compared with those obtained from healthy controls and patients with another autoimmune disease such as multiple sclerosis. Results. Levels of MxA mRNA above the 99th percentile of values found in healthy controls were observed in 9 out of 50 patients with SSc (p < 0.001). Induced MxA expression was significantly associated with some features of more severe disease, such as lower forced vital capacity and the presence of ischemic digital ulcers. No differences in the levels of IFNAR were found within MxA-induced and MxA-non-induced patients, but there was a direct correlation between levels of MxA and the soluble isoform of IFNAR2. Conclusion. Our results show induction of MxA expression in some patients with SSc, which correlates with the presence of ischemic ulcers and other signs of worse disease, suggesting a potential role of Type I IFN in the pathogenesis of this disease and/or its complications. (First Release Oct 1 2008; J Rheumatol 2008;35:2192-200: doi: 10.3899/jrheum.080418)
引用
收藏
页码:2192 / 2200
页数:9
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