Sumi Tamaki, Fukushima Atsuki, Nishino Koji, Fukuda Ken, Kumagai Naoki, Nishida Teruo, Ueno Hisayuki
Department of Ophthalmology and Visual Science, Kochi Medical School, Kohasu, Oko-cho, Nankoku-city, Japan.
Cell Biol Int. 2009 Apr;33(4):534-41. doi: 10.1016/j.cellbi.2009.02.002. Epub 2009 Feb 20.
To investigate whether experimental allergic conjunctivitis (EC) can be suppressed by treatment with the immunomodulatory drug FTY720, which reduces the recruitment of effector T cells into inflammatory sites.
BALB/c mice were actively immunized with ragweed (RW) and then injected intraperitoneally with FTY720 on days 0, 2, 4, 6 and 8 (induction phase treatment) followed by challenge on day 10 with RW-containing eye drops. Alternatively, naïve mice that received RW-primed splenocytes were injected intraperitoneally with FTY720 on days 2 and 4 (effector phase treatment) followed by RW challenge on day 4. Twenty-four hours after RW challenge, conjunctivas and spleens were harvested for histology or immunohistochemistry, and flow cytometric analysis or cytokine assays, respectively.
FTY720 treatment during the induction phase suppressed the conjunctival infiltration of T cells as well as eosinophils and macrophages. The splenocytes from induction phase-treated mice contained significantly less CD4(+) and CD8(+) T cells and showed significant suppression of Th2 but not Th1 cytokine production. Effector phase treatment with FTY720 suppressed conjunctival eosinophil infiltration.
These data demonstrate that FTY720 treatment during the induction phase decreases the absolute number of CD4(+) and CD8(+) T cells in the spleen and suppresses Th2 cytokine production by splenocytes. This leads to the suppression of EC. FTY720 treatment also suppresses EC when delivered during the effector phase. Thus, FTY720 treatment may be suitable for treating severe forms of vernal keratoconjunctivitis.
研究免疫调节药物FTY720能否抑制实验性变应性结膜炎(EC),该药物可减少效应T细胞向炎症部位的募集。
用豚草(RW)对BALB/c小鼠进行主动免疫,然后在第0、2、4、6和8天腹腔注射FTY720(诱导期治疗),随后在第10天用含RW的滴眼液进行激发。或者,对接受过RW致敏脾细胞的未致敏小鼠在第2和4天腹腔注射FTY720(效应期治疗),然后在第4天进行RW激发。RW激发24小时后,分别采集结膜和脾脏用于组织学或免疫组织化学检查,以及流式细胞术分析或细胞因子检测。
诱导期使用FTY720治疗可抑制T细胞以及嗜酸性粒细胞和巨噬细胞在结膜的浸润。诱导期治疗小鼠的脾细胞中CD4(+)和CD8(+) T细胞明显减少,Th2细胞因子产生受到显著抑制,但Th1细胞因子产生未受抑制。效应期使用FTY720治疗可抑制结膜嗜酸性粒细胞浸润。
这些数据表明,诱导期使用FTY720治疗可减少脾脏中CD4(+)和CD8(+) T细胞的绝对数量,并抑制脾细胞产生Th2细胞因子。这导致EC受到抑制。效应期使用FTY720治疗也可抑制EC。因此,FTY720治疗可能适用于治疗严重形式的春季角结膜炎。