Patterson R, Suszko I M, Harris K E
J Clin Invest. 1978 Sep;62(3):519-24. doi: 10.1172/JCI109155.
Rhesus monkeys with airway responses to aerosol challenge with Ascaris antigen constitute a primate model of inhalant asthma. Previous studies have shown that bronchial lavage cells from airway-reactive animals will release histamine or a slow-reactive substance of anaphylaxis after challenge with antigen. Because these bronchial lumen cells are the first cells in contact with inhaled antigen, they may play a role in induction of antigen-induced airway responses. To evaluate this possibility, bronchial lumen lavage cells from animals with airway reactivity were transferred to the bronchial lumens of animals with negative airway responses to antigen challenge. The transfer of the bronchial lumen cells resulted in transient airway reactivity of the recipients to aerosol antigen challenge. It is suggested that the mast cells which constitute a component of the bronchial lumen cells may be the active cell alone, or in combination with other cells, which results in this primate immunoglobulin E-mediated airway response and its transfer to nonreactivie recipients.
对蛔虫抗原气雾剂激发有气道反应的恒河猴构成了吸入性哮喘的灵长类动物模型。先前的研究表明,来自气道反应性动物的支气管灌洗细胞在抗原激发后会释放组胺或过敏反应慢反应物质。由于这些支气管腔细胞是与吸入抗原接触的首批细胞,它们可能在抗原诱导的气道反应的诱导中发挥作用。为评估这种可能性,将具有气道反应性动物的支气管腔灌洗细胞转移到对抗原激发气道反应阴性的动物的支气管腔中。支气管腔细胞的转移导致受体对气雾剂抗原激发产生短暂的气道反应性。有人提出,构成支气管腔细胞成分的肥大细胞可能单独或与其他细胞一起成为活性细胞,这导致了这种灵长类动物免疫球蛋白E介导的气道反应及其向无反应受体的转移。