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In vitro detection of cytotoxic T and NK cells in peripheral blood of patients with various drug-induced skin diseases

机译:多种药物性皮肤病患者外周血细胞毒性T和NK细胞的体外检测

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Background: Cytotoxic cells are involved in most forms of drug-induced skin diseases. Till now, no in vitro test addressed this aspect of drug-allergic responses. Our report evaluates whether drug-induced cytotoxic cells can be detected in peripheral blood of nonacute patients with different forms of drug hypersensitivity, and also whether in vitro detection of these cells could be helpful in drug-allergy diagnosis.Methods: GranzymeB enzyme-linked immunosorbent spot-forming (ELISPOT) and cell surface expression of the degranulation marker CD 107a were evaluated on peripheral blood mononuclear cells from 12 drug-allergic patients in remission state and 16 drug-exposed healthy controls.Results: In 10/12 allergic patients culprit but not irrelevant drug elicited granzymeB release after 48-72 h stimulation. It was clearly positive in patients with high prolif-erative response to the drug, measured in lymphocyte transformation tests. In patients, who showed moderate or low proliferation and low drug-response in granzymeB ELISPOT, overnight preincubation with interleukin (IL)-7/IL-15 enhanced drug-specific granzymeB release and allowed to clearly identify the offending agent. CD107a staining was positive on CD4 + /CD3 + , CD8 + /CD3+ T cells as well as CD56 + /CD3- natural killer cells. None of the drug-exposed healthy donors reacted to the tested drugs and allergic patients reacted only to the offending, but not to tolerated drugs.Conclusion: GranzymeB ELISPOT is a highly specific in vitro method to detect drug-reacting cytotoxic cells in peripheral blood of drug-allergic patients even several years after disease manifestation. Together with IL-7/IL-15 preincubation, it may be helpful in indentifying the offending drug even in some patients with weak proliferative drug-response.
机译:背景:细胞毒性细胞参与大多数形式的药物诱发的皮肤疾病。到目前为止,还没有体外试验解决药物过敏反应的这一方面。我们的报告评估了是否可以在具有不同形式药物超敏反应的非急性患者的外周血中检测到药物诱导的细胞毒性细胞,以及在体外检测这些细胞是否有助于药物过敏诊断。在12名处于缓解状态的药物过敏患者和16名暴露于药物的健康对照者的外周血单核细胞上评价了脱颗粒标记CD 107a的斑点形成(ELISPOT)和细胞表面表达。结果:10/12过敏患者是罪魁祸首,无关的药物在刺激48-72小时后引起粒酶B释放。在淋巴细胞转化试验中测得,对这种药物有高增殖反应的患者显然是阳性的。在GranzymeB ELISPOT中显示中度或低度增殖和低药物反应的患者中,与白介素(IL)-7 / IL-15一起进行的过夜预孵育增强了药物特异性颗粒酶B的释放,并可以清楚地鉴定出有问题的药物。 CD107a染色在CD4 + / CD3 +,CD8 + / CD3 + T细胞以及CD56 + / CD3-自然杀伤细胞上呈阳性。结论:GranzymeB ELISPOT是一种高度特异性的体外方法,可以检测受试药物的健康供体,而对耐受药物则无反应。药物过敏的患者甚至在疾病表现后的几年内。与IL-7 / IL-15预温育一起使用,即使在某些增殖性药物反应较弱的患者中,也可能有助于鉴定有问题的药物。

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