Kumar Seema, Bahn Rebecca S
Division of Pediatric Endocrinology, Clinic, Rochester, Minnesota 55905, USA.
J Clin Endocrinol Metab. 2003 Sep;88(9):4246-50. doi: 10.1210/jc.2003-030380.
Graves' ophthalmopathy (GO) is an autoimmune disorder involving the adipose and connective tissues of the orbit. The study of cytokines present in these tissues may reveal the nature of the cells and immune responses involved in GO pathogenesis. In the current study, we performed relative quantification of the expression of cytokine genes in orbital adipose tissue from patients with GO (n = 6) and normal individuals (n = 2). Real-time RT-PCR was performed using fluorescent probes and primers for cytokines including IL-1 beta, IL-2, IL-4, IL-5, IL-8, IL-10, IFN-gamma, and TNF-alpha. Results showed IL-1 beta to be the gene having the greatest fold expression increase over normal in four of six patients. TNF-alpha was increased in all six GO patients. In addition, IL-8, IL-10, and IFN-gamma were increased in five of six GO patients. We found no evidence of either IL-4 or IL-5 expression in any of the GO or normal samples. The increased expression of the macrophage-derived cytokines IL-1 beta, TNF-alpha, and IL-10 suggests the presence of macrophage activation and ongoing antigen presentation within the orbit in GO. In addition, the overexpression of IFN-gamma, without evidence of IL-4 or IL-5 expression, supports the concept that cell-mediated, rather than humoral, immunity plays the predominant role in pathogenesis of this disorder.
格雷夫斯眼病(GO)是一种累及眼眶脂肪和结缔组织的自身免疫性疾病。对这些组织中存在的细胞因子进行研究,可能会揭示参与GO发病机制的细胞性质和免疫反应。在本研究中,我们对GO患者(n = 6)和正常个体(n = 2)眼眶脂肪组织中细胞因子基因的表达进行了相对定量分析。使用针对包括白细胞介素-1β(IL-1β)、白细胞介素-2(IL-2)、白细胞介素-4(IL-4)、白细胞介素-5(IL-5)、白细胞介素-8(IL-8)、白细胞介素-10(IL-10)、干扰素-γ(IFN-γ)和肿瘤坏死因子-α(TNF-α)等细胞因子的荧光探针和引物进行实时逆转录聚合酶链反应(RT-PCR)。结果显示,在6例患者中的4例中,IL-1β是表达倍数相对于正常增加最大的基因。所有6例GO患者的TNF-α均升高。此外,6例GO患者中的5例IL-8、IL-10和IFN-γ升高。我们在任何GO或正常样本中均未发现IL-4或IL-5表达的证据。巨噬细胞衍生的细胞因子IL-1β、TNF-α和IL-10表达增加,提示GO患者眼眶内存在巨噬细胞活化和持续的抗原呈递。此外,IFN-γ的过表达,且无IL-4或IL-5表达的证据,支持细胞介导而非体液免疫在该疾病发病机制中起主要作用的观点。