Henson P M, Pinckard R N
Monogr Allergy. 1977;12:13-26.
Evidence is presented that IgE-induced, basophil-derived, platelet-activating factor (PAF) causes sequestration of rabbit platelets during sublethal IgE-induced anaphylaxis, and produces a state of specific desensitization in the platelets upon their subsequent return to the circulation. Moreover, depletion of platelets from rabbits undergoing lethal anaphylaxis abrogated the mortality and markedly reduced other parameters of the anaphylaxis. It was suggested that PAF may represent a major mediator of this reaction. A number of lines of evidence have suggested in addition that PAF may play a role in acute experimental immune complex disen that PAF may play a role in acute experimental immune complex disease in rabbits by causing release of vasoactive amines from platelets, lase in rabbits by causing release of vasoactive amines from platelets, leading to increased vascular permeability and deposition of circulating immune complexes along filtering vascular membranes. This data, providing evidence for the action of PAF in vivo and implicating this action in two allergic reactions, supports the contention that PAF is an important mediator of acute allergic reactions.
有证据表明,在亚致死性IgE诱导的过敏反应中,IgE诱导的、嗜碱性粒细胞衍生的血小板活化因子(PAF)会导致兔血小板滞留,并在血小板随后返回循环时使其产生特异性脱敏状态。此外,在致死性过敏反应的兔中消耗血小板可消除死亡率,并显著降低过敏反应的其他参数。有人提出PAF可能是该反应的主要介质。此外,一些证据还表明,PAF可能通过使血小板释放血管活性胺,在兔急性实验性免疫复合物疾病中发挥作用,导致血管通透性增加以及循环免疫复合物沿滤过血管膜沉积。这些数据为PAF在体内的作用提供了证据,并表明其作用与两种过敏反应有关,支持了PAF是急性过敏反应重要介质的论点。