Yoshida H, Yoshida O, Iwamoto H, Nishino K, Hashida M, Fukushima A, Ueno H
Department of Ophthalmology, Kochi Medical School, Nankoku, Japan.
Br J Ophthalmol. 1998 Oct;82(10):1189-94. doi: 10.1136/bjo.82.10.1189.
To analyse the role of stimulation in vitro of lymphocytes on the augmentation of experimental immune mediated blepharoconjunctivitis (EC, formerly EAC) in Lewis rats induced by adoptive transfer.
Two weeks after immunisation with ovalbumin (OVA), rat draining lymph nodes were collected and 50 x 10(6) cells were injected into naive syngeneic recipients either directly or after culture in vitro with OVA, concanavalin A (Con A), or purified protein derivative (PPD) for 3 days. Four days after injection the rats were topically challenged with OVA. 24 hours later, they were sacrificed and eyes and spleens were harvested for histology and proliferation assay. In some experiments, naive recipient rats were irradiated with 7 Gy gamma ray before transfer. The expression of adhesion molecules and cytokine profile of OVA primed lymph node cells were also investigated.
Both infiltrated cell number and splenocyte proliferation in the recipients of stimulated cells were higher than those of unstimulated cells. In vitro stimulation with OVA or Con A induced a severe cellular infiltration, while stimulation with PPD did not. Irradiation markedly diminished cellular infiltration. Stimulation in vitro upregulated the CD4/CD8 ratio by four times and augmented expression of CD25, I-A, ICAM-1 molecules on OVA primed lymph node cells by about five times. IFN-gamma was detected in OVA primed cells by stimulation in vitro, while IL-4 mRNA was extinguished by stimulation in vitro.
Augmentation of EC by stimulation in vitro of transferred lymphocytes might depend on the upregulation of expression of cell surface molecules and cytokine shift as well as augmented antigen specificity.
分析体外刺激淋巴细胞对过继转移诱导的Lewis大鼠实验性免疫介导性睑结膜炎(EC,原EAC)加重的作用。
用卵清蛋白(OVA)免疫两周后,收集大鼠引流淋巴结,将50×10⁶个细胞直接注入同基因未致敏受体,或在体外与OVA、刀豆蛋白A(Con A)或纯化蛋白衍生物(PPD)培养3天后注入。注射4天后,用OVA对大鼠进行局部攻击。24小时后,处死大鼠,取眼和脾脏进行组织学检查和增殖测定。在一些实验中,未致敏受体大鼠在转移前接受7 Gyγ射线照射。还研究了OVA致敏淋巴结细胞的黏附分子表达和细胞因子谱。
刺激细胞受体中的浸润细胞数和脾细胞增殖均高于未刺激细胞。用OVA或Con A进行体外刺激诱导了严重的细胞浸润,而用PPD刺激则未诱导。照射明显减少了细胞浸润。体外刺激使OVA致敏淋巴结细胞上的CD4/CD8比值上调了四倍,CD25、I-A、ICAM-1分子的表达增加了约五倍。体外刺激在OVA致敏细胞中检测到干扰素-γ,而白细胞介素-4 mRNA在体外刺激后消失。
体外刺激转移的淋巴细胞加重EC可能取决于细胞表面分子表达的上调、细胞因子的转变以及抗原特异性的增强。