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海藻糖和透明质酸联合疗法通过改善干眼患者眼表的炎症反应蛋白标志物来恢复泪液脂质层功能。

Combination Therapy with Trehalose and Hyaluronic Acid Restores Tear Lipid Layer Functionality by Ameliorating Inflammatory Response Protein Markers on the Ocular Surface of Dry Eye Patients.

作者信息

Perumal Natarajan, Manicam Caroline, Jeong Eunjin, Runde Sarah, Pfeiffer Norbert, Grus Franz H

机构信息

Experimental and Translational Ophthalmology, Department of Ophthalmology, University Medical Centre of the Johannes Gutenberg University Mainz, Langenbeckstr. 1, DE-55131 Mainz, Germany.

出版信息

J Clin Med. 2025 Aug 5;14(15):5525. doi: 10.3390/jcm14155525.

Abstract

Topical lubricants are the fundamental treatment for dry eye disease (DED). However, the molecular mechanisms underlying their efficacy remain unknown. Here, the protective effects of Thealoz Duo with 3% trehalose and 0.15% hyaluronic acid are investigated in DED patients by a longitudinal clinical study and subsequent elucidation of the tear proteome and cell signaling changes. Participants were classified as moderate to severe DED (DRY, = 35) and healthy (CTRL, = 23) groups. Specific DED subgroups comprising evaporative (DRYlip) and aqueous-deficient with DRYlip (DRYaqlip) were also classified. Only DED patients received Thealoz Duo. All participants were clinically examined before (day 0, T1) and after the application of Thealoz Duo at day 28 (T2) and day 56 (T3). Next, 174 individual tear samples from all groups at three time-points were subjected to proteomics analysis. Clinically, Thealoz Duo significantly improved the ocular surface disease index at T2 vs. T1 (DRY, = 1.4 × 10; DRYlip, = 9.2 × 10) and T3 vs. T1 (DRY, = 2.1 × 10; DRYlip, = 1.2 × 10), and the tear break-up time at T3 vs. T1 (DRY, = 3.8 × 10; DRYlip, = 1.4 × 10). Thealoz Duo significantly ameliorated expression of inflammatory response proteins ( < 0.05) at T3, which was observed at T1 (DRY, = 3.4 × 10; DRYlip, = 7.1 × 10; DRYaqlip, = 2.7 × 10). Protein S100-A8 (S100A8), Alpha-1-antitrypsin (SERPINA1), Annexin A1 (ANXA1), and Apolipoprotein A-I (APOA1) were found to be significantly reduced in all the DED subgroups. The application of Thealoz Duo showed the therapeutic characteristic of the anti-inflammatory mechanism by promoting the expression of (Metalloproteinase inhibitor 1) TIMP1 in all the DED subgroups. Thealoz Duo substantially improved the DED symptoms and restored the functionality of the tear lipid layer to near normal in DRYlip and DRY patients by ameliorating inflammation. Notably, this study unravels the novel mechanistic alterations underpinning the healing effects of Thealoz Duo in DED subgroups in a time-dependent manner, which supports the improvement in corresponding clinical attributes.

摘要

局部润滑剂是干眼症(DED)的基本治疗方法。然而,其疗效背后的分子机制尚不清楚。在此,通过纵向临床研究以及随后对泪液蛋白质组和细胞信号变化的阐释,研究了含3%海藻糖和0.15%透明质酸的Thealoz Duo对DED患者的保护作用。参与者被分为中度至重度DED组(DRY,n = 35)和健康组(CTRL,n = 23)。还划分了包括蒸发过强型(DRYlip)和伴有蒸发过强型的泪液分泌不足型(DRYaqlip)在内的特定DED亚组。仅DED患者接受Thealoz Duo治疗。所有参与者在第0天(T1)、第28天(T2)和第56天(T3)使用Thealoz Duo之前和之后均接受临床检查。接下来,对所有组在三个时间点的174份个体泪液样本进行蛋白质组学分析。临床上,与T1相比,Thealoz Duo在T2时显著改善了眼表疾病指数(DRY组,n = 1.4×10;DRYlip组,n = 9.2×10)以及T3时与T1相比的情况(DRY组,n = 2.1×10;DRYlip组,n = 1.2×10),并且在T3时与T1相比泪膜破裂时间也显著改善(DRY组,n = 3.8×10;DRYlip组,n = 1.4×10)。Thealoz Duo在T3时显著改善了炎症反应蛋白的表达(P < 0.05),这在T1时也有观察到(DRY组,n = 3.4×10;DRYlip组,n = 7.1×10;DRYaqlip组,n = 2.7×10)。发现蛋白质S100 - A8(S100A8)、α - 1抗胰蛋白酶(SERPINA1)、膜联蛋白A1(ANXA1)和载脂蛋白A - I(APOA1)在所有DED亚组中均显著降低。Thealoz Duo的应用通过促进所有DED亚组中金属蛋白酶抑制剂1(TIMP1)的表达显示出抗炎机制的治疗特性。Thealoz Duo通过减轻炎症显著改善了DED症状,并使DRYlip和DRY患者泪液脂质层的功能恢复至接近正常。值得注意的是,本研究揭示了Thealoz Duo在DED亚组中以时间依赖性方式产生愈合作用的新机制改变,这支持了相应临床指标的改善。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecc2/12347701/a5d763aea811/jcm-14-05525-g001.jpg

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