Alcon Laboratories, USA.
Department of Optometry and Vision Science, School of Optometry, University of Alabama at Birmingham, Birmingham, AL, USA.
Cont Lens Anterior Eye. 2022 Jun;45(3):101442. doi: 10.1016/j.clae.2021.101442. Epub 2021 Apr 3.
To evaluate the levels and regulation of tear film inflammatory proteins in contact lens-related dry eye (CLDE).
One hundred healthy, daily wear (non-overnight), experienced soft contact lens wearers were classified into normal (n = 50) and CLDE (n = 50) groups based on Contact Lens and Dry Eye Questionnaire scores, tear break-up times, and comfort (a two-hour difference between total and comfortable daily lens wear hours). Tear samples (up to 5 μL) were collected by capillary extraction from the inferior meniscus of each eye, and pooled tear samples (10 per group) were tested using a customized Quantibody array. Mann Whitney tests with the Benjamini-Hochberg procedure with a 5% false discovery rate were used to compare the normal and CLDE groups.
Relative to the normal group, the CLDE group showed a significantly increased tear concentration of several inflammatory mediators, including interleukin (IL)-7 (p = 0.001), IL-8 (p = 0.001), IL-13 (p = 0.001), IL-15 (p = 0.001), IL-12 p70 (p = 0.002), growth-related oncogene-alpha/ chemokine (CXC motif) ligand 1 (p = 0.003), granulocyte-colony stimulating factor (p = 0.005), IL-11 (p = 0.008), epidermal growth factor receptor (p = 0.01), IL-1 receptor antagonist (RA) (p = 0.013), macrophage colony-stimulating factor (p = 0.013), Eotaxin/CC motif chemokine ligand 11 (CCL11) (p = 0.016), and IL-2 (p = 0.016). The following cytokines were increased three-fold or more in the CLDE group: IL-13 (p = 0.001), Eotaxin/CCL11 (p = 0.016), and IL-1RA (p = 0.013).
Several inflammatory markers, including interleukins, were increased in tears of subjects with CLDE. These results support a growing body of evidence that suggests a potential role of inflammation in CLDE.
评估接触镜相关干眼(CLDE)患者泪膜中炎症蛋白的水平和调节。
根据接触镜和干眼问卷评分、泪膜破裂时间和舒适度(总戴镜时间与舒适戴镜时间相差 2 小时),将 100 名健康、日戴(非过夜)、有经验的软性隐形眼镜佩戴者分为正常组(n=50)和 CLDE 组(n=50)。通过毛细管提取从每只眼睛的下穹隆采集泪样(最多 5 μL),并使用定制的 Quantibody 阵列测试每组 10 个 pooled 泪样。采用 Mann Whitney 检验和 Benjamini-Hochberg 程序(假发现率为 5%)比较正常组和 CLDE 组。
与正常组相比,CLDE 组的几种炎症介质的泪液浓度显著增加,包括白细胞介素(IL)-7(p=0.001)、IL-8(p=0.001)、IL-13(p=0.001)、IL-15(p=0.001)、IL-12 p70(p=0.002)、生长相关癌基因-α/趋化因子(CXC 基序)配体 1(p=0.003)、粒细胞集落刺激因子(p=0.005)、IL-11(p=0.008)、表皮生长因子受体(p=0.01)、IL-1 受体拮抗剂(RA)(p=0.013)、巨噬细胞集落刺激因子(p=0.013)、嗜酸性粒细胞趋化因子/CC 基序趋化因子配体 11(CCL11)(p=0.016)和 IL-2(p=0.016)。CLDE 组中以下细胞因子增加了三倍或更多:IL-13(p=0.001)、Eotaxin/CCL11(p=0.016)和 IL-1RA(p=0.013)。
CLDE 患者的泪液中存在多种炎症标志物,包括白细胞介素。这些结果支持越来越多的证据表明炎症可能在 CLDE 中发挥作用。