An interferon signature in the peripheral blood of dermatomyositis patients is associated with disease activity

被引:224
作者
Baechler, Emily C.
Bauer, Jason W.
Slattery, Catherine A.
Ortmann, Ward A.
Espe, Karl J.
Novitzke, Jill
Ytterberg, Steven R.
Gregersen, Peter K.
Behrens, Timothy W.
Reed, Ann M.
机构
[1] Mayo Clin & Mayo Grad Sch Med, Div Rheumatol, Dept Med, Rochester, MN 55902 USA
[2] Mayo Clin & Mayo Grad Sch Med, Div Rheumatol, Dept Pediat, Rochester, MN 55902 USA
[3] Univ Minnesota, Sch Med, Minneapolis, MN 55455 USA
[4] N Shore Long Isl Jewish Res Inst, Feinstein Inst Med Res, Manhasset, NY 11030 USA
关键词
D O I
10.2119/2006-00085.Baechler
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Recent studies have shown increased expression of interferon (IFN)-regulated genes in the peripheral blood cells of patients with systemic lupus erythematosus. A similar interferon signature has been observed in affected muscle tissue from patients with dermatomyositis (DM), but it has not yet been determined if this signature extends to the peripheral blood in DM. We performed global gene expression profiling of peripheral blood cells from adult and juvenile DM patients and healthy controls. Several interesting groups of genes were differentially expressed in DM, including genes with immune function, and others that function in muscle or are involved in mitochondrial/oxidative phosphorylation. Investigation of type I IFN-regulated transcripts revealed a striking interferon signature present in most DM patients studied. Levels of type I IFN-regulated proteins were also elevated in DM serum samples. Furthermore, both the transcript and serum protein IFN signatures were associated with disease activity. These data suggest that the IFN signature may be a useful marker for DM disease activity, and that sampling peripheral blood may be a more practical alternative to muscle biopsy for measuring this signature.
引用
收藏
页码:59 / 68
页数:10
相关论文
共 46 条
  • [41] Cell death and oxidative damage in inflammatory myopathies
    Tews, DS
    Goebel, HH
    [J]. CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1998, 87 (03): : 240 - 247
  • [42] Gene expression profiling in DQA1*0501+ children with untreated dermatomyositis:: A novel model of pathogenesis
    Tezak, Z
    Hoffman, EP
    Lutz, JL
    Fedczyna, TO
    Stephan, D
    Bremer, EG
    Krasnoselska-Riz, I
    Kumar, A
    Pachman, LM
    [J]. JOURNAL OF IMMUNOLOGY, 2002, 168 (08) : 4154 - 4163
  • [43] Significance analysis of microarrays applied to the ionizing radiation response
    Tusher, VG
    Tibshirani, R
    Chu, G
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (09) : 5116 - 5121
  • [44] KIR in type 1 diabetes: Disparate distribution of activating and inhibitory natural killer cell receptors in patients versus HLA-matched control subjects
    van der Slik, AR
    Koeleman, BPC
    Verduijn, W
    Bruining, GJ
    Roep, BO
    Giphart, MJ
    [J]. DIABETES, 2003, 52 (10) : 2639 - 2642
  • [45] Zhou XD, 2004, MED SCI MONITOR, V10, pBR191
  • [46] ZurWiesch AS, 2004, CLIN EXP RHEUMATOL, V22, P368