Federal Institute for Drugs and Medical Devices, 53175 Bonn, Germany.
Br J Dermatol. 2011 Jan;164(1):68-75. doi: 10.1111/j.1365-2133.2010.10055.x.
Beginning in 2007, anaphylactoid reactions associated with unfractionated heparin (UFH) occurred and resulted in some fatalities. These reactions were reported to be linked to the complement and contact system activation induced by certain batches of UFH containing the adulterant oversulphated chondroitin sulphate (OSCS).
Drug-specific secretion of selected cytokines from peripheral blood mononuclear cells (PBMC) of patients with hypersensitivity reactions to contaminated heparin was compared with the respective in vitro cytokine pattern of individuals with or without hypersensitivity to heparin, different glycosaminoglycans or other drugs.
Study individuals (n = 13) were classified as follows: patients with hypersensitivity reactions to contaminated (OSCS) heparin (n = 3), noncontaminated heparin (n = 1) or other compounds (n = 3) and patients with ongoing heparin therapy without symptoms of intolerance (n = 2). Four healthy individuals served as controls. PBMC were incubated with six different glycosaminoglycan structures. Drug-specific intracellular interleukin (IL)-5, interferon (IFN)-γ and IL-10 production was investigated by flow cytometry, while secretion of IL-5, IL-2 and IFN-γ was analysed by enzyme-linked immunosorbent assay.
PBMC from individuals with hypersensitivity reactions to contaminated heparin secreted considerable amounts of IL-2 in vitro. There was a suggestion that ongoing heparin therapy and the Li-heparin in the vials may have an impact on the lymphocyte reactivity of PBMC.
The in vitro lymphocyte reactivity pattern of PBMC from individuals with hypersensitivity reactions to contaminated heparins was neither typical for an immune-mediated nor for a nonimmune-mediated reaction. Possible effects of heparins in the test system itself may require consideration.
自 2007 年以来,与未分级肝素(UFH)相关的过敏样反应发生,并导致一些死亡。这些反应据报道与某些批次的 UFH 中含有的杂质过度硫酸软骨素(OSCS)引起的补体和接触系统激活有关。
比较过敏反应患者对污染肝素的外周血单个核细胞(PBMC)中特定细胞因子的药物特异性分泌与对肝素、不同糖胺聚糖或其他药物无过敏反应个体的相应体外细胞因子模式。
研究个体(n=13)分为以下几类:对污染(OSCS)肝素(n=3)、非污染肝素(n=1)或其他化合物(n=3)过敏反应的患者,以及正在接受肝素治疗且无不耐受症状的患者(n=2)。4 名健康个体作为对照。将 PBMC 与六种不同的糖胺聚糖结构孵育。通过流式细胞术研究药物特异性细胞内白细胞介素(IL)-5、干扰素(IFN)-γ和 IL-10 的产生,通过酶联免疫吸附试验分析 IL-5、IL-2 和 IFN-γ的分泌。
对污染肝素过敏反应的个体的 PBMC 体外大量分泌 IL-2。有迹象表明,正在进行的肝素治疗和小瓶中的 Li 肝素可能对 PBMC 的淋巴细胞反应性产生影响。
对污染肝素过敏反应患者的 PBMC 体外淋巴细胞反应性模式既不是免疫介导的,也不是非免疫介导的反应。测试系统本身中肝素的可能影响需要考虑。