Chen Ling, Holland Gary N, Yu Fei, Levinson Ralph D, Lampi Kirsten J, Horwitz Joseph, Gordon Lynn K
Departments of 2Ophthalmology, Ocular Inflammatory Disease Center, Jules Stein Eye Institute, University of California, Los Angeles, California 90095-7000, USA.
Invest Ophthalmol Vis Sci. 2008 Oct;49(10):4476-81. doi: 10.1167/iovs.08-1971. Epub 2008 Jun 6.
betaB1-crystallin is a putative target of an autoantibody observed in a subset of patients with uveitis. The purpose of this study was to determine whether seroreactivity against betaB1 or other specific purified crystallin proteins is observed in patients with uveitis and whether this reactivity is associated with either cataract or active intraocular inflammation.
Sera from patients with uveitis were tested for IgG antibodies with reactivity against alphaA-, alphaB-, betaB1-, or betaB2-crystallin proteins using a modified slot-blot protocol. Ophthalmic evaluations included analysis of the degree of intraocular inflammation and assessment of lens opacity by the Lens Opacities Classification System (LOCS) III. Positive anti-crystallin reactivity was defined as greater than the mean + 2 SD of the reactivity of a commercially available control serum panel. Statistical analysis was performed with the Fisher exact test, Kruskal-Wallis test, and Student's t-test.
IgG antibodies against alphaA-, alphaB-, or betaB1-crystallin were identified in 70% of 39 subjects; in contrast, only 30% of the control sera exhibited reactivity against one or more of these crystallin proteins (P <or= 0.01). Seroreactivity against alphaA-, alphaB-, or betaB1-, but not betaB2-crystallin was related to active anterior segment inflammation. Seroreactivity against alphaB and betaB1 was significantly related to cortical cataract (P <or= 0.05).
Serum antibodies against specific crystallin proteins are present in most patients with uveitis. The relationship between the presence of specific anti-crystallin antibodies and active inflammation may indicate a role for these autoantibodies in uveitis pathogenesis.
βB1-晶体蛋白是在一部分葡萄膜炎患者中观察到的自身抗体的假定靶标。本研究的目的是确定葡萄膜炎患者中是否存在针对βB1或其他特定纯化晶体蛋白的血清反应性,以及这种反应性是否与白内障或活动性眼内炎症相关。
采用改良的狭缝印迹法检测葡萄膜炎患者血清中针对αA-、αB-、βB1-或βB2-晶体蛋白的IgG抗体。眼科评估包括分析眼内炎症程度和通过晶状体混浊分类系统(LOCS)III评估晶状体混浊情况。抗晶体蛋白反应阳性定义为高于市售对照血清组反应性的均值 + 2标准差。采用Fisher精确检验、Kruskal-Wallis检验和Student t检验进行统计分析。
39名受试者中有70%检测到针对αA-、αB-或βB1-晶体蛋白的IgG抗体;相比之下,仅30%的对照血清对这些晶体蛋白中的一种或多种表现出反应性(P≤0.01)。针对αA-、αB-或βB1-而非βB2-晶体蛋白的血清反应性与眼前节活动性炎症相关。针对αB和βB1的血清反应性与皮质性白内障显著相关(P≤0.05)。
大多数葡萄膜炎患者体内存在针对特定晶体蛋白的血清抗体。特定抗晶体蛋白抗体的存在与活动性炎症之间的关系可能表明这些自身抗体在葡萄膜炎发病机制中起作用。