Fukushima Atsuki, Yamaguchi Tomoko, Ishida Waka, Fukata Kazuyo, Liu Fu-Tong, Ueno Hisayuki
Department of Ophthalmology, Kochi Medical School, Kochi University, Kohasu, Oko-cho, Nankoku-city, Japan.
Clin Exp Ophthalmol. 2006 May-Jun;34(4):347-53. doi: 10.1111/j.1442-9071.2006.01221.x.
Eosinophils are important effector cells in severe allergic conjunctivitis such as vernal keratoconjunctivitis. Infiltration of eosinophils into the conjunctiva is mediated by type I and type IV allergic reactions. Cyclosporin A (CsA) eye drops are administered therapeutically for severe allergic conjunctivitis, but the mechanism by which CsA acts, that is, by inhibiting type I, type IV or both types of allergic reactions, is not known. We investigated whether CsA eye drops inhibit type I, type IV or both types of allergic reactions in the conjunctiva.
Experimental immune-mediated blepharoconjunctivitis (EC) was induced in BALB/c mice by either active immunization or passive immunization by transfer of ragweed (RW)-primed splenocytes and RW-specific IgE, followed by RW challenge to the conjunctiva. These mice were treated in eye drops with vehicle, 0.1% CsA, 0.5% CsA or 0.1% betamethasone five times (1 and 2 h before RW challenge and 1, 2 and 3 h after RW challenge). Twenty-four hours after the challenge, the conjunctivas were harvested for histological analysis to evaluate eosinophilic infiltration. To evaluate effects of CsA eye drops on systemic immune responses, sera and spleens were collected from actively immunized mice at the time of sacrifice to examine serum IgE levels and cellular immune responses, respectively.
CsA eye drops significantly inhibited eosinophilic infiltration into the conjunctiva in actively immunized EC-developing mice compared with vehicle-treated mice. The CsA-induced inhibition was similar to inhibition induced by 0.1% betamethasone. Serum IgE levels and splenocyte responses in CsA-treated mice were equivalent to those in vehicle-treated mice. Betamethasone treatment inhibited eosinophilic infiltration into the conjunctiva induced by both splenocyte transfer and IgE transfer, while CsA treatment inhibited infiltration induced by splenocyte transfer.
CsA eye drops inhibited eosinophilic infiltration into the conjunctiva without affecting systemic immune responses. CsA predominantly inhibits eosinophilic infiltration by interfering with the type IV allergic reaction in the conjunctiva.
嗜酸性粒细胞是严重过敏性结膜炎(如春季角结膜炎)中的重要效应细胞。嗜酸性粒细胞向结膜的浸润由I型和IV型过敏反应介导。环孢素A(CsA)滴眼液用于治疗严重过敏性结膜炎,但其作用机制,即抑制I型、IV型或两种类型的过敏反应,尚不清楚。我们研究了CsA滴眼液是否抑制结膜中的I型、IV型或两种类型的过敏反应。
通过主动免疫或通过转移豚草(RW)致敏的脾细胞和RW特异性IgE进行被动免疫,随后对结膜进行RW激发,在BALB/c小鼠中诱导实验性免疫介导的睑结膜炎(EC)。这些小鼠用赋形剂、0.1% CsA、0.5% CsA或0.1%倍他米松滴眼液处理五次(在RW激发前1小时和2小时以及RW激发后1小时、2小时和3小时)。激发后24小时,收集结膜进行组织学分析以评估嗜酸性粒细胞浸润。为了评估CsA滴眼液对全身免疫反应的影响,在处死时从主动免疫的小鼠收集血清和脾脏,分别检查血清IgE水平和细胞免疫反应。
与赋形剂处理的小鼠相比,CsA滴眼液显著抑制了主动免疫的EC发生小鼠结膜中的嗜酸性粒细胞浸润。CsA诱导的抑制作用与0.1%倍他米松诱导的抑制作用相似。CsA处理的小鼠的血清IgE水平和脾细胞反应与赋形剂处理的小鼠相当。倍他米松处理抑制了脾细胞转移和IgE转移诱导的结膜嗜酸性粒细胞浸润,而CsA处理抑制了脾细胞转移诱导的浸润。
CsA滴眼液抑制结膜中的嗜酸性粒细胞浸润而不影响全身免疫反应。CsA主要通过干扰结膜中的IV型过敏反应来抑制嗜酸性粒细胞浸润。