García-Zepeda Sihomara, Estrada-Muñiz Elizabet, Elizondo Guillermo, Terrazas Luis I, Rodríguez-Sosa Miriam, Quintana-Hau Juan D, Tornero-Montaño Rubén, Baiza-Durán Leopoldo, Vega Libia
Departamento de Toxicología, Centro de Investigación y de Estudios Avanzados- IPN. Av. IPN 2508, San Pedro Zacatenco, México D.F. 07360, México;
Open Ophthalmol J. 2012;6:129-36. doi: 10.2174/1874364101206010129. Epub 2012 Dec 14.
BACKGROUND #ENTITYSTARTX00026;
Levocetirizine is a histamine H(1) receptor antagonist. Here, we utilised DO11.10TCR transgenic mice to establish an antigen-specific T cell-dependent allergic conjunctivitis (AC) model to determine the effect of the topical application of an ophthalmic formulation of Levoceritizine as a treatment for AC.
DO11.10 mice (n=6/each) were exposed to ovalbumin (OVA, 50 µg) and treated with a Levocetirizine ophthalmic formulation (0.001-0.02% v/w) or placebo (vehicle) for 24-72 h. Serum, aqueous/vitreous humour and conjunctiva were obtained. Immunoglobulin (Ig)-E, interleukin (IL)-10 and lipoxin (LX)A(4) were determined by ELISA. Levels of tumour necrosis factor (TNF)-α, transforming growth factor (TGF)-β, interferon (IFN)-γ and 18rS expression were measured by RT-PCR. Proportions of total and activated antigen-presenting cells (APC), recruited T lymphocytes (CD4+), activated T lymphocytes (CD25+) and T regulatory cells (Treg) were measured by flow cytometry.
OVA exposure induced AC in the animal model indicated by increased expression of LXA(4), TNF-α and TGF-β. Levocetirizine treatment (0.01-0.02% v/w) reduced LXA(4) in the eye humours. This treatment approach increased systemic IL-10 secretion and reduced TNF-α and TGF-β expression in conjunctiva without changing IFN-γ expression. Levocetirizine reduced APC levels in draining lymph nodes but increased the proportion of total lymphocytes recruited and their differentiation to Treg cells. CONCLUSIONS #ENTITYSTARTX00026;
Levocetirizine effectively reduces the activation and migration of APC to local draining lymph nodes and induces differentiation of Treg cells as one possible mechanism of its anti-inflammatory action.
背景
左西替利嗪是一种组胺H(1)受体拮抗剂。在此,我们利用DO11.10TCR转基因小鼠建立抗原特异性T细胞依赖性过敏性结膜炎(AC)模型,以确定局部应用左西替利嗪眼用制剂治疗AC的效果。
将DO11.10小鼠(每组n = 6)暴露于卵清蛋白(OVA,50μg),并用左西替利嗪眼用制剂(0.001 - 0.02% v/w)或安慰剂(赋形剂)治疗24 - 72小时。获取血清、房水/玻璃体和结膜。通过酶联免疫吸附测定法(ELISA)测定免疫球蛋白(Ig)-E、白细胞介素(IL)-10和脂氧素(LX)A(4)。通过逆转录聚合酶链反应(RT-PCR)测量肿瘤坏死因子(TNF)-α、转化生长因子(TGF)-β、干扰素(IFN)-γ和18rS表达水平。通过流式细胞术测量总抗原呈递细胞(APC)和活化抗原呈递细胞、募集的T淋巴细胞(CD4+)、活化的T淋巴细胞(CD25+)和调节性T细胞(Treg)的比例。
OVA暴露在动物模型中诱导了AC,表现为LXA(4)、TNF-α和TGF-β表达增加。左西替利嗪治疗(0.01 - 0.02% v/w)降低了眼液中的LXA(4)。这种治疗方法增加了全身IL-10分泌,并降低了结膜中TNF-α和TGF-β表达,而不改变IFN-γ表达。左西替利嗪降低了引流淋巴结中的APC水平,但增加了募集的总淋巴细胞比例及其向Treg细胞的分化。
结论
左西替利嗪有效地减少了APC向局部引流淋巴结的活化和迁移,并诱导Treg细胞分化,这是其抗炎作用的一种可能机制。