Brignole F, Pisella P J, Goldschild M, De Saint Jean M, Goguel A, Baudouin C
Laboratory of Immunohematology, Ambroise Paré Hospital, Assistance Publique-Hopitaux de Paris, University of Paris-V René Descartes, France.
Invest Ophthalmol Vis Sci. 2000 May;41(6):1356-63.
To investigate in impression cytology (IC) specimens the expression of inflammatory and apoptosis-related markers by conjunctival epithelial cells from patients with dry eye as a rationale for treatment with topical cyclosporine.
Immunologic anomalies were identified at baseline, before treatment with the masked medication, in a homogeneous series of patients with dry eye syndrome, who were enrolled in a large European multicenter clinical trial (Cyclosporin A Dry Eye Study; Allergan, Irvine, CA). IC specimens were collected in 243 patients with moderate to severe keratoconjunctivitis sicca (KCS), with or without Sjogren's syndrome (SS). Fifty normal subjects were separately examined to provide normal control values. Specimens were analyzed in a masked manner by flow cytometry, using antibodies directed to markers of the immune system and/or apoptotic pathway: HLA DR, CD40, CD40 ligand, Fas, and APO2.7. Levels of expression were quantified, and results were compared with those obtained in the 50 normal patients.
One hundred sixty-nine specimens were successfully interpreted at baseline, including 41% from patients with SS. A highly significant increase of HLA DR expression by conjunctival cells was found in KCS-affected eyes compared with normal eyes, which did not express this marker or did so very weakly. HLA DR expression in eyes with SS was significantly higher than in KCS-affected eyes without SS. Fas and APO2.7 were found at low levels in all normal and KCS-affected eyes. CD40 and CD40 ligand expressions were significantly increased in eyes with KCS compared with normal eyes. HLA DR, CD40 and Fas were found at significantly higher levels in the SS group than in the non-SS group. CONCLUSIONS. Conjunctival cells from patients with dry eye with moderate to severe KCS, with or without SS, overexpress inflammatory and apoptosis-related markers. Whether inflammation is a primary phenomenon in KCS or is the consequence of repetitive abrasion of the ocular surface after tear film deficiency remains to be determined. These data, nevertheless, support the use of immunomodulatory and/or anti-inflammatory drugs in the treatment of patients with KCS.
通过对干眼症患者结膜上皮细胞进行印迹细胞学(IC)标本分析,研究炎症和凋亡相关标志物的表达情况,以此作为局部应用环孢素治疗的理论依据。
在一项大型欧洲多中心临床试验(环孢素A干眼症研究;Allergan,尔湾,加利福尼亚州)中,对一组同质的干眼症综合征患者在使用盲法药物治疗前进行基线免疫异常检测。收集了243例中重度干燥性角结膜炎(KCS)患者的IC标本,这些患者伴有或不伴有干燥综合征(SS)。另外对50名正常受试者进行单独检测以提供正常对照值。使用针对免疫系统和/或凋亡途径标志物的抗体,通过流式细胞术对标本进行盲法分析:HLA DR、CD40、CD40配体、Fas和APO2.7。对表达水平进行定量,并将结果与50名正常患者的结果进行比较。
169份标本在基线时成功解读,其中41%来自SS患者。与正常眼相比,KCS受累眼中结膜细胞HLA DR表达显著增加,正常眼不表达或表达非常微弱。SS患者眼中HLA DR表达显著高于无SS的KCS受累眼。在所有正常眼和KCS受累眼中,Fas和APO2.7水平较低。与正常眼相比,KCS患者眼中CD40和CD40配体表达显著增加。SS组中HLA DR、CD40和Fas水平显著高于非SS组。结论:中重度KCS患者(伴有或不伴有SS)的结膜细胞过度表达炎症和凋亡相关标志物。炎症是KCS的原发性现象还是泪膜缺乏后眼表反复摩擦的结果仍有待确定。然而,这些数据支持在KCS患者治疗中使用免疫调节和/或抗炎药物。