Contreras-Ruiz Laura, Mir Fayaz A, Turpie Bruce, Krauss Achim H, Masli Sharmila
Schepens Eye Research Inst. and Massachusetts Eye and Ear, Department of Ophthalmology Harvard Medical School, Boston, MA, USA.
GSK Ophthalmology, King of Prussia, PA, USA.
Exp Eye Res. 2016 Feb;143:1-8. doi: 10.1016/j.exer.2015.10.008. Epub 2015 Oct 14.
Sjögren's syndrome is an autoimmune disease associated with inflammation of exocrine glands with clinical manifestations of dry eye and dry mouth. Dry eye in this disease involves inflammation of the ocular surface tissues - cornea and conjunctiva. While systemic blockade of adhesion molecules has been used to treat autoimmune diseases, the purpose of this study was to determine the therapeutic efficacy of topical application of an integrin α4 adhesion molecule antagonist in a mouse model of dry eye associated with Sjögren's syndrome. To assess this spontaneously developed ocular surface inflammation related to Sjögren's syndrome in TSP-1null mice (12 wks) was evaluated. Mice were treated with topical formulations containing 0.1% dexamethasone or 30 mg/ml GW559090 or vehicle control. Corneal fluorescein staining and conjunctival goblet cell density were assessed. Real-time PCR analysis was performed to assess expression of the inflammatory marker IL-1β in the cornea and Tbet and RORγt in the draining lymph nodes. Ocular surface inflammation was detectable in TSP-1null mice (≥12 wk old), which resulted in increased corneal fluorescein staining indicative of corneal barrier disruption and reduced conjunctival goblet cell density. These changes were accompanied by increased corneal expression of IL-1β as compared to WT controls and an altered balance of Th1 (Tbet) and Th17 (RORγt) markers in the draining lymph nodes. Topically applied dexamethasone and GW559090 significantly reduced corneal fluorescein staining compared to vehicle treatment (p = 0.023 and p < 0.001, respectively). This improved corneal barrier integrity upon adhesion molecule blockade was consistent with significantly reduced corneal expression of pro-inflammatory IL-1β compared to vehicle treated groups (p < 0.05 for both treatments). Significant improvement in goblet cell density was also noted in mice treated with 0.1% dexamethasone and GW559090 (p < 0.05 for both). We conclude that similar to topical dexamethasone, topically administered GW559090 successfully improved corneal barrier integrity and inflammation in an established ocular surface disease associated with Sjögren's syndrome.
干燥综合征是一种自身免疫性疾病,与外分泌腺炎症相关,临床表现为干眼和口干。该疾病中的干眼涉及眼表组织(角膜和结膜)的炎症。虽然全身阻断黏附分子已被用于治疗自身免疫性疾病,但本研究的目的是确定在与干燥综合征相关的干眼小鼠模型中局部应用整合素α4黏附分子拮抗剂的治疗效果。为了评估这种与干燥综合征相关的自发发生的眼表炎症,对TSP-1基因敲除小鼠(12周龄)进行了评估。小鼠用含有0.1%地塞米松或30mg/ml GW559090的局部制剂或赋形剂对照进行治疗。评估角膜荧光素染色和结膜杯状细胞密度。进行实时PCR分析以评估角膜中炎症标志物IL-1β以及引流淋巴结中Tbet和RORγt的表达。在TSP-1基因敲除小鼠(≥12周龄)中可检测到眼表炎症,这导致角膜荧光素染色增加,表明角膜屏障破坏,结膜杯状细胞密度降低。与野生型对照相比,这些变化伴随着角膜中IL-1β表达增加以及引流淋巴结中Th1(Tbet)和Th17(RORγt)标志物平衡改变。与赋形剂治疗相比,局部应用地塞米松和GW559090显著降低了角膜荧光素染色(分别为p = 0.023和p < 0.001)。与赋形剂治疗组相比,黏附分子阻断后角膜屏障完整性的改善与角膜促炎IL-1β表达显著降低一致(两种治疗均p < 0.05)。在用0.1%地塞米松和GW559090治疗的小鼠中也观察到杯状细胞密度有显著改善(两种治疗均p < 0.05)。我们得出结论,与局部应用地塞米松类似,局部应用GW559090成功改善了与干燥综合征相关的已建立的眼表疾病中的角膜屏障完整性和炎症。