Latalska Małgorzata, Gerkowicz Marek, Kosior-Jarecka Ewa, Kozioł-Montewka Maria, Pietraś-Trzpiel Małgorzata
II Kliniki Okulistyki Akademii Medycznej im. prof. Feliksa Skubiszewskiego w Lublinie.
Klin Oczna. 2004;106(1-2 Suppl):162-3.
Evaluation of the serum and aqueous humor antibodies to beta-2 glycoprotein I in patients with glaucoma.
48 persons (38 women and 17 men), aged 30-86 (mean age 70), suffering from glaucoma was examined. There were 19 with POAG, 18 with PACG and 11 with PEXG. All patients have undergone trabeculectomy. The group of 20 operated patients, because of age-related cataracta (7 men and 13 women), aged 47-82 (mean age 65), constituted a control group. All patients agreed with samples collection. In plasma and anterior chamber fluid, the level of antibodies to b-2 glycoprotein I classes IgA and IgG were measured using ELISA method (commercial kits produced by Euroimmun), according to producer's instruction. Statistical analysis was performed using U Mann-Whitney test when both groups were compared and Spearman test to comparisons concerning single group.
Significant changes between glaucoma and cataract patients were observed in anti-b-2 glycoprotein I antibodies class IgA in aqueous humour (p=0.04) and in serum (p=0.03).
Knowledge of the immunological pathogenesis in the glaucomatous nerve damage can be curtailed or even prevented with the use of proper agents. Indeed, there are many intriguing new therapeutic possibilities on the horizon. To determine the clinical potential of serum antibodies in glaucoma patients, a randomized clinical trial would be necessary. It is the preliminary communication.
评估青光眼患者血清和房水中抗β2糖蛋白I抗体。
对48例年龄在30 - 86岁(平均年龄70岁)的青光眼患者(38名女性和17名男性)进行检查。其中原发性开角型青光眼19例,原发性闭角型青光眼18例,剥脱性青光眼11例。所有患者均接受了小梁切除术。20例因年龄相关性白内障接受手术的患者(7名男性和13名女性),年龄在47 - 82岁(平均年龄65岁),构成对照组。所有患者均同意采集样本。采用ELISA法(Euroimmun生产的商业试剂盒),按照生产商说明,检测血浆和前房液中抗β2糖蛋白I的IgA和IgG类抗体水平。两组比较时采用U曼-惠特尼检验进行统计学分析,单组比较采用Spearman检验。
青光眼患者与白内障患者相比,房水中抗β2糖蛋白I的IgA类抗体(p = 0.04)和血清中该抗体(p = 0.03)存在显著差异。
通过使用合适的药物,可以减少甚至预防青光眼性神经损伤的免疫发病机制。确实,未来有许多有趣的新治疗可能性。为确定青光眼患者血清抗体的临床潜力,有必要进行一项随机临床试验。这是初步报道。