Weber F, Hempel K
Institute of Medical Radiation Research, University of Würzburg, FRG.
Int Arch Allergy Appl Immunol. 1989;89(2-3):242-5. doi: 10.1159/000234953.
Pretreatment with complete Freund's adjuvant blended with aluminium hydroxide (ALU-CFA) prevents the clinical as well as histological manifestation of experimental allergic encephalomyelitis (EAE) in Lewis rats. Suppression of prostaglandin biosynthesis with the cyclooxygenase inhibitor piroxicam (10 mg/kg body weight) from day 2 before to day 17 after EAE induction could not restore responsiveness in pretreated animals. In contrast piroxicam increased ALU-CFA-induced suppression of autoantibodies against myelin basic protein. In controls not pretreated with ALU-CFA, clinical signs of EAE were attenuated by piroxicam, whereas mononuclear infiltration of the brain remained unchanged. Therefore it is unlikely that prostaglandins exert an important function in the regulation of immune responses in this model of autoimmunity.
用完全弗氏佐剂与氢氧化铝混合(ALU-CFA)进行预处理,可预防Lewis大鼠实验性变态反应性脑脊髓炎(EAE)的临床及组织学表现。从EAE诱导前2天到诱导后17天,用环氧化酶抑制剂吡罗昔康(10毫克/千克体重)抑制前列腺素生物合成,无法恢复预处理动物的反应性。相反,吡罗昔康增强了ALU-CFA诱导的针对髓鞘碱性蛋白自身抗体的抑制作用。在未用ALU-CFA预处理的对照中,吡罗昔康减轻了EAE的临床症状,而脑内单核细胞浸润保持不变。因此,在这种自身免疫模型中,前列腺素不太可能在免疫反应调节中发挥重要作用。