Rosenbaum J T, Planck S T, Huang X N, Rich L, Ansel J C
Department of Ophthalmology, Casey Eye Institute, Oregon Health Sciences University, Portland 97201, USA.
Invest Ophthalmol Vis Sci. 1995 Sep;36(10):2151-5.
Cytokines have been implicated in corneal inflammatory diseases. The authors sought to determine if corneal diseases with different patterns of inflammation are accompanied by characteristic patterns of cytokine expression.
The authors used reverse transcription-polymerase chain reaction to detect mRNA for 12 specific cytokines from patients with Fuch's dystrophy (n = 7), pseudophakic bullous keratopathy (n = 12), or normal corneas (n = 4).
Using Wilcoxon rank sum analysis, mRNA for interleukin (IL)-1 alpha or IL-8 was significantly more abundant in corneas from patients with pseudophakic bullous keratopathy relative to either comparison group. mRNA for the T-cell marker, CD4, and for T-cell derived cytokines, IL-2, IL-4, and interferon gamma, could not be detected in any corneal sample. Message for IL-1 receptor antagonist and transforming growth factor-beta 1 or -beta 2 was readily detectable in most corneas regardless of diagnosis.
The findings indicate that the pattern of cytokine mRNA expression reflects differences in the pathogenesis of these corneal diseases.
细胞因子与角膜炎症性疾病有关。作者试图确定具有不同炎症模式的角膜疾病是否伴有细胞因子表达的特征性模式。
作者使用逆转录聚合酶链反应检测了来自富克斯营养不良患者(n = 7)、人工晶状体性大泡性角膜病变患者(n = 12)或正常角膜(n = 4)的12种特定细胞因子的mRNA。
使用威尔科克森秩和分析,相对于任何一个对照组,人工晶状体性大泡性角膜病变患者角膜中的白细胞介素(IL)-1α或IL-8的mRNA含量显著更高。在任何角膜样本中均未检测到T细胞标志物CD4以及T细胞衍生细胞因子IL-2、IL-4和干扰素γ的mRNA。无论诊断如何,在大多数角膜中均可轻易检测到IL-1受体拮抗剂以及转化生长因子-β1或-β2的信息。
研究结果表明细胞因子mRNA表达模式反映了这些角膜疾病发病机制的差异。