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本文引用的文献

1
Follistatin-like protein 1 is a mesenchyme-derived inflammatory protein and may represent a biomarker for systemic-onset juvenile rheumatoid arthritis.卵泡抑素样蛋白1是一种间充质来源的炎症蛋白,可能是全身型幼年特发性关节炎的生物标志物。
Arthritis Rheum. 2010 Aug;62(8):2510-6. doi: 10.1002/art.27485.
2
Methotrexate withdrawal at 6 vs 12 months in juvenile idiopathic arthritis in remission: a randomized clinical trial.缓解期幼年特发性关节炎中 6 个月与 12 个月时停用甲氨蝶呤:一项随机临床试验。
JAMA. 2010 Apr 7;303(13):1266-73. doi: 10.1001/jama.2010.375.
3
Systemic JIA: new developments in the understanding of the pathophysiology and therapy.全身型幼年特发性关节炎:对发病机制和治疗的新认识。
Best Pract Res Clin Rheumatol. 2009 Oct;23(5):655-64. doi: 10.1016/j.berh.2009.08.003.
4
Role of Wnt-5A in interleukin-1beta-induced matrix metalloproteinase expression in rabbit temporomandibular joint condylar chondrocytes.Wnt-5A在白细胞介素-1β诱导兔颞下颌关节髁突软骨细胞基质金属蛋白酶表达中的作用
Arthritis Rheum. 2009 Sep;60(9):2714-22. doi: 10.1002/art.24779.
5
IL-1 beta promotes A549 cell migration via MAPKs/AP-1- and NF-kappaB-dependent matrix metalloproteinase-9 expression.白细胞介素-1β通过丝裂原活化蛋白激酶/活化蛋白-1和核因子κB依赖性基质金属蛋白酶-9的表达促进A549细胞迁移。
Cell Signal. 2009 Nov;21(11):1652-62. doi: 10.1016/j.cellsig.2009.07.002. Epub 2009 Jul 16.
6
Diagnostic value of procalcitonin for differentiation between bacterial infection and non-infectious inflammation in febrile patients with active adult-onset Still's disease.降钙素原在成年起病的Still病活动期发热患者中对细菌感染与非感染性炎症的鉴别诊断价值
Ann Rheum Dis. 2009 Jun;68(6):1074-5. doi: 10.1136/ard.2008.098335.
7
Comparative analysis of synovial fluid and plasma proteomes in juvenile arthritis--proteomic patterns of joint inflammation in early stage disease.青少年关节炎滑液和血浆蛋白质组的比较分析——疾病早期关节炎症的蛋白质组模式
J Proteomics. 2009 May 2;72(4):656-76. doi: 10.1016/j.jprot.2009.01.022.
8
Depletion of one, six, twelve or twenty major blood proteins before proteomic analysis: the more the better?在蛋白质组学分析之前去除一种、六种、十二种或二十种主要血液蛋白质:越多越好?
J Proteomics. 2009 Aug 20;72(6):945-51. doi: 10.1016/j.jprot.2009.03.008. Epub 2009 Mar 31.
9
The myeloid-related proteins 8 and 14 complex, a novel ligand of toll-like receptor 4, and interleukin-1beta form a positive feedback mechanism in systemic-onset juvenile idiopathic arthritis.髓样相关蛋白8和14复合物,一种Toll样受体4的新型配体,与白细胞介素-1β在全身型幼年特发性关节炎中形成正反馈机制。
Arthritis Rheum. 2009 Mar;60(3):883-91. doi: 10.1002/art.24349.
10
A unique plasma proteomic profiling with imbalanced fibrinogen cascade in patients with Kawasaki disease.川崎病患者存在独特的血浆蛋白质组特征及纤维蛋白原级联失衡。
Pediatr Allergy Immunol. 2009 Nov;20(7):699-707. doi: 10.1111/j.1399-3038.2008.00844.x. Epub 2009 Jan 12.

活动期全身型幼年特发性关节炎的血浆谱:生物标志物及其生物学意义。

Plasma profiles in active systemic juvenile idiopathic arthritis: Biomarkers and biological implications.

机构信息

Department of Pediatrics, Stanford University, Stanford, CA 94305-5164, USA.

出版信息

Proteomics. 2010 Dec;10(24):4415-30. doi: 10.1002/pmic.201000298. Epub 2010 Nov 23.

DOI:10.1002/pmic.201000298
PMID:21136595
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3517169/
Abstract

Systemic juvenile idiopathic arthritis (SJIA) is a chronic arthritis of children characterized by a combination of arthritis and systemic inflammation. There is usually non-specific laboratory evidence of inflammation at diagnosis but no diagnostic test. Normalized volumes from 89/889 2-D protein spots representing 26 proteins revealed a plasma pattern that distinguishes SJIA flare from quiescence. Highly discriminating spots derived from 15 proteins constitute a robust SJIA flare signature and show specificity for SJIA flare in comparison to active polyarticular juvenile idiopathic arthritis or acute febrile illness. We used 7 available ELISA assays, including one to the complex of S100A8/S100A9, to measure levels of 8 of the15 proteins. Validating our DIGE results, this ELISA panel correctly classified independent SJIA flare samples, and distinguished them from acute febrile illness. Notably, data using the panel suggest its ability to improve on erythrocyte sedimentation rate or C-reactive protein or S100A8/S100A9, either alone or in combination in SJIA F/Q discriminations. Our results also support the panel's potential clinical utility as a predictor of incipient flare (within 9 wk) in SJIA subjects with clinically inactive disease. Pathway analyses of the 15 proteins in the SJIA flare versus quiescence signature corroborate growing evidence for a key role for IL-1 at disease flare.

摘要

全身型幼年特发性关节炎(SJIA)是一种儿童慢性关节炎,其特征为关节炎和全身炎症的组合。通常在诊断时有非特异性炎症的实验室证据,但没有诊断性检查。代表 26 种蛋白质的 89/889 个 2-D 蛋白质点的归一化体积揭示了一种区分 SJIA 发作与静止的血浆模式。源自 15 种蛋白质的高度区分斑点构成了一个强大的 SJIA 发作特征,并显示出与活动性多关节型幼年特发性关节炎或急性发热性疾病相比,对 SJIA 发作的特异性。我们使用了 7 种可用的 ELISA 测定法,包括一种用于 S100A8/S100A9 复合物的测定法,来测量 15 种蛋白质中的 8 种蛋白质的水平。验证我们的 DIGE 结果,该 ELISA 面板正确地对独立的 SJIA 发作样本进行了分类,并将它们与急性发热性疾病区分开来。值得注意的是,使用该面板的数据表明,它能够提高红细胞沉降率或 C 反应蛋白或 S100A8/S100A9 的性能,无论是单独使用还是在 SJIA F/Q 鉴别中联合使用。我们的结果还支持该面板作为具有临床静止疾病的 SJIA 患者即将发作(在 9 周内)的预测因子的潜在临床效用。在 SJIA 发作与静止签名中的 15 种蛋白质的途径分析证实了白细胞介素-1 在疾病发作中的关键作用的证据不断增加。