Clinical Research Department, London School of Hygiene and Tropical Medicine, London WC1E 7HT, UK.
Kilimanjaro Christian Medical Centre, PO Box 3010, Moshi, Kilimanjaro, Tanzania.
Pathog Dis. 2017 Mar 1;75(2). doi: 10.1093/femspd/ftx016.
We previously showed that conjunctival miR-147b and miR-1285 were upregulated in Gambian adults with inflammatory scarring trachoma, and miR-155 and miR-184 expression was strongly associated with conjunctival inflammation and ocular Chlamydia trachomatis infection in children from Guinea-Bissau. We investigated whether the single or combined expression of miR-147b, miR-1285, miR-155 and miR-184 was able to identify individuals with increased risk of incident or progressive scarring trachoma. Conjunctival swab samples were collected from 506 children between the ages of 4 and 12 living in northern Tanzania. These 506 samples formed the baseline sample set of a 4-year longitudinal study. Chlamydia trachomatis infection was diagnosed by droplet digital PCR and expression of miR-155, miR-184, miR-1285 and miR-147b was tested by qPCR. Individuals were assessed for incidence and progression of conjunctival scarring by comparison of conjunctival photographs taken at baseline and 4 years later. miR-184 and miR-155 were strongly associated with inflammation and infection at baseline; however, no miR was associated with 4-year scarring incidence or progression. miR-184 expression was more strongly downregulated during inflammation in non-progressors relative to progressors, suggesting that a disequilibrium in the efficiency of wound healing is a significant determinant of progressive conjunctival fibrosis.
我们之前的研究表明,在冈比亚患有炎症性瘢痕性沙眼的成年人中,结膜 miR-147b 和 miR-1285 的表达上调,而 miR-155 和 miR-184 的表达与来自几内亚比绍的儿童的结膜炎症和眼部沙眼衣原体感染密切相关。我们研究了 miR-147b、miR-1285、miR-155 和 miR-184 的单一或联合表达是否能够识别患有复发性或进行性瘢痕性沙眼风险增加的个体。我们从居住在坦桑尼亚北部的 506 名 4 至 12 岁的儿童中收集了结膜拭子样本。这些 506 个样本构成了一项为期 4 年的纵向研究的基线样本集。通过液滴数字 PCR 诊断沙眼衣原体感染,并通过 qPCR 测试 miR-155、miR-184、miR-1285 和 miR-147b 的表达。通过比较基线和 4 年后拍摄的结膜照片,评估个体结膜瘢痕形成的发生率和进展情况。miR-184 和 miR-155 与基线时的炎症和感染密切相关;然而,没有 miR 与 4 年的瘢痕形成发生率或进展相关。与进展者相比,非进展者的炎症期间 miR-184 的表达下调更明显,这表明伤口愈合效率的失衡是进行性结膜纤维化的重要决定因素。