Jørgensen K T, Wiik A, Pedersen M, Hedegaard C J, Vestergaard B F, Gislefoss R E, Kvien T K, Wohlfahrt J, Bendtzen K, Frisch M
Department of Epidemiology Research, Statens Serum Institut, 5 Artillerivej, DK-2300 Copenhagen, Denmark.
Ann Rheum Dis. 2008 Jun;67(6):860-6. doi: 10.1136/ard.2007.073825. Epub 2007 Jul 20.
OBJECTIVE: To assess the timing of changes in cytokines, cytokine-related markers, autoantibodies and viral antibodies in the pathogenesis of rheumatoid arthritis (RA). METHODS: Case-control study nested in a prospective cohort of 31 330 blood donors in Oslo, Norway. Forty-nine donors developed RA up to 23 years after their most recent blood donation. Stored sera from these donors (case sera) and a sex- and age-matched sample of 245 healthy donors (control sera), and postdiagnostic sera from 33 of the 49 RA cases, were analysed for a panel of cytokines and cytokine-related markers, autoantibodies and antibodies against Epstein-Barr virus and parvovirus B19. RESULTS: Cytokines and cytokine-related markers were generally negative in case sera from >5 years before the diagnosis of RA. In the 5-year interval immediately before the diagnosis of RA, more case than control sera were positive (odds ratios >2) for interleukin (IL)-1 alpha, IL-1 beta, IL-1 receptor antagonist, IL-4, IL-10, tumour necrosis factor-alpha and soluble tumour necrosis factor receptor I. In postdiagnostic sera, however, 11 of 16 examined cytokines and cytokine-related markers were statistically significantly elevated compared with control sera. Seropositivity for IgG antibodies against cyclic citrullinated peptides and for IgM and IgA rheumatoid factors were seen in case sera from up to 18 years before the diagnosis of RA. IgG antibodies against Epstein-Barr virus and parvovirus B19 did not differ significantly between case and control sera. CONCLUSIONS: Cytokines and cytokine-related markers appear to be upregulated rather late in RA pathogenesis. In contrast, IgM rheumatoid factor and IgG anti-cyclic citrullinated peptide autoantibodies may precede the diagnosis of RA by up to two decades.
目的:评估细胞因子、细胞因子相关标志物、自身抗体及病毒抗体在类风湿关节炎(RA)发病机制中的变化时间。 方法:在挪威奥斯陆的31330名献血者的前瞻性队列中进行病例对照研究。49名献血者在最近一次献血后长达23年时患上类风湿关节炎。对这些献血者的储存血清(病例血清)、245名性别和年龄匹配的健康献血者的样本(对照血清)以及49例RA病例中33例的诊断后血清进行了一系列细胞因子、细胞因子相关标志物、自身抗体以及抗爱泼斯坦 - 巴尔病毒和细小病毒B19抗体的分析。 结果:在RA诊断前>5年的病例血清中,细胞因子和细胞因子相关标志物通常为阴性。在RA诊断前的5年间隔期内,病例血清中白细胞介素(IL)-1α、IL-1β、IL-1受体拮抗剂、IL-4、IL-10、肿瘤坏死因子-α和可溶性肿瘤坏死因子受体I呈阳性的比例高于对照血清(优势比>2)。然而,在诊断后血清中,与对照血清相比,所检测的16种细胞因子和细胞因子相关标志物中有11种在统计学上显著升高。在RA诊断前长达18年的病例血清中可检测到抗环瓜氨酸肽IgG抗体以及IgM和IgA类风湿因子的血清阳性。病例血清和对照血清中抗爱泼斯坦 - 巴尔病毒和细小病毒B19的IgG抗体无显著差异。 结论:细胞因子和细胞因子相关标志物在RA发病机制中似乎上调较晚。相比之下,IgM类风湿因子和IgG抗环瓜氨酸肽自身抗体可能在RA诊断前长达二十年就已出现。
Ann Rheum Dis. 2013-12-13
Medicina (Kaunas). 2024-11-26