Serum IgG levels of sensitized guinea-pigs bled at various times after the booster injection were evaluated and its capacity to sensitize passively lung strips from normal guinea-pigs assessed. Following the booster injection, both serum IgG and the ability to sensitize passively lung strips increased during the first week and decreased slowly thereafter. 2. The PAF antagonist WEB 2086 (3 mg kg-1, i.v.) blocked the anaphylactic bronchoconstriction induced by intravenous administration of ovalbumin (1 mg kg-1) when guinea-pigs were challenged 2 and 4 days after the booster injection, but became ineffective when tested in guinea-pigs challenged 7, 28 and 56 days after the booster injection. 3. The ability of WEB 2086 to reduce anaphylactic bronchoconstriction of guinea-pigs challenged 2 and 4 days after the booster injection was unrelated to either the selective involvement of one type of immunoglobulin, low IgG titres in sera or a reduced sensitizing capacity. 4. The booster injection, which accounts for the loss of efficacy of WEB 2086 from the fourth day thereafter, probably operates as a PAF-independent inflammatory challenge. 5. The protocol for immunisation and the day of experiment after the booster injection determines the sensitivity of the anaphylactic bronchoconstriction to inhibition of PAF antagonists.
摘要
对加强注射后不同时间采血的致敏豚鼠血清IgG水平进行评估,并测定其被动致敏正常豚鼠肺条的能力。加强注射后,血清IgG和被动致敏肺条的能力在第一周均升高,此后缓慢下降。2. 血小板活化因子(PAF)拮抗剂WEB 2086(3毫克/千克,静脉注射)可阻断加强注射后2天和4天静脉注射卵清蛋白(1毫克/千克)诱导的过敏性支气管收缩,但在加强注射后7天、28天和56天进行激发试验的豚鼠中无效。3. WEB 2086减轻加强注射后2天和4天激发的豚鼠过敏性支气管收缩的能力,与某一种免疫球蛋白的选择性参与、血清中低IgG滴度或致敏能力降低均无关。4. 加强注射导致此后第四天起WEB 2086失效,可能作为一种不依赖PAF的炎性刺激发挥作用。5. 免疫方案及加强注射后的实验日期决定过敏性支气管收缩对PAF拮抗剂抑制作用的敏感性。