Desquand S, Lefort J, Liu F T, Mencia-Huerta J M, Vargaftig B B
Unité de Pharmacologie Cellulaire, Unité Associée Institut Pasteur/INSERM, Paris, France.
Int Arch Allergy Appl Immunol. 1989;89(1):71-7. doi: 10.1159/000234926.
A selective model to study the IgE-mediated anaphylactic bronchoconstriction (BC) in the guinea pig is needed, since human asthma involves mainly this class of antibody. However, most procedures presently available for passive homologous or active sensitization lead to responses which are mediated both by IgE and IgG antibodies. In this study, we developed an anaphylactic model in which guinea pigs are passively sensitized with mouse ascitic fluid containing dinitrophenol (DNP)-specific IgE antibodies. Challenge of sensitized animals with DNP coupled to bovine serum albumin evokes a bronchoconstrictor response that is maximal 5 h after sensitization. The resulting anaphylactic BC is not blocked by the H1 histamine antagonist mepyramine, by the peptido-leukotriene antagonist FLP 55712 nor by the platelet-activating factor antagonist BN 52021 alone. However, when the sensitized animals are pretreated with the three drugs in combination, significantly reduced BC was observed upon challenge with the antigen. This latter result indicates that IgE-dependent BC involves the participation of different mediators, a characteristic shared in common with allergic asthma in human.
由于人类哮喘主要涉及这类抗体,因此需要一种选择性模型来研究豚鼠中IgE介导的过敏性支气管收缩(BC)。然而,目前用于被动同源致敏或主动致敏的大多数方法都会导致由IgE和IgG抗体介导的反应。在本研究中,我们建立了一种过敏性模型,其中用含有二硝基苯酚(DNP)特异性IgE抗体的小鼠腹水对豚鼠进行被动致敏。用与牛血清白蛋白偶联的DNP攻击致敏动物会引起支气管收缩反应,该反应在致敏后5小时达到最大。所产生的过敏性BC不会被H1组胺拮抗剂美吡拉敏、肽白三烯拮抗剂FLP 55712或单独的血小板活化因子拮抗剂BN 52021阻断。然而,当用这三种药物联合预处理致敏动物时,在用抗原攻击后观察到BC明显降低。后一结果表明,IgE依赖性BC涉及不同介质的参与,这是人类过敏性哮喘共有的特征。