Jappe U, Gollnick H
Klinik und Poliklinik für Dermatologie und Venerologie, Otto-von-Guericke Universität Magdeburg.
Hautarzt. 1999 Jun;50(6):406-11. doi: 10.1007/s001050050932.
The pathogenesis of allergic reactions to heparin is poorly understood. Clinically, this phenomenon is very relevant because of its increasing incidence and the resulting therapeutic difficulties. Since Plancherel's first description in 1952, nearly 70 cases have been reported in the literature, among which female patients dominate. Heparin causes all kind of allergic reactions from type I to type IV. The most dangerous hypersensitivity reaction is heparin-induced thrombocytopenia (HIT), which is a type II antibody-mediated reaction. Heparin is a mucopolysaccharide with strong protein binding potency, which seems to play an important pathogenetic role, as the heparin molecule adheres to unknown dermal or subcutaneous proteins. The heparin group contains a variety of structures with varying molecular weights. The allergen has yet to be identified. Several cross-reactions between high- and low-molecular weight heparins have been demonstrated as well as between heparin and heparinoids so that there may be more than one epitope of the heparin molecule with allergic potency. Allergic reactions after the use of alternate drugs such as heparinoids and hirudin also causes severe therapeutic difficulties.
肝素过敏反应的发病机制尚不清楚。临床上,由于其发病率不断上升以及由此产生的治疗困难,这一现象非常值得关注。自1952年普兰谢雷尔首次描述以来,文献中已报道了近70例病例,其中女性患者占主导。肝素可引起从I型到IV型的各种过敏反应。最危险的超敏反应是肝素诱导的血小板减少症(HIT),这是一种II型抗体介导的反应。肝素是一种具有强蛋白结合能力的粘多糖,似乎起着重要的致病作用,因为肝素分子会附着在未知的皮肤或皮下蛋白质上。肝素类包含多种分子量不同的结构。过敏原尚未确定。已证实高分子量肝素和低分子量肝素之间以及肝素与类肝素之间存在多种交叉反应,因此肝素分子可能有不止一个具有过敏活性的表位。使用类肝素和水蛭素等替代药物后的过敏反应也会导致严重的治疗困难。