Department of Clinical and Environmental Allergology, Jagiellonian University Medical College, Krakow, Poland.
Department of Clinical and Environmental Allergology, Jagiellonian University Medical College, Krakow, Poland.
J Immunol Methods. 2021 Aug;495:113062. doi: 10.1016/j.jim.2021.113062. Epub 2021 Apr 30.
In patients with drug hypersensitivity reactions, confirmation of causality frequently facilitates decision on a continuation or withdrawal of a given treatment. Unfortunately, identification of the culprit drug often proves difficult. In vivo methods possess well-known disadvantages like low sensitivity of skin tests or the risk of relapse during drug provocation tests. Therefore, laboratory assays are of great interest as they may improve causal diagnosis without putting patients at risk. In this article, the mechanistic principles and methodological issues of the enzyme-linked immunospot (ELISpot) assay were recapped the context of drug hypersensitivity reactions. A review of ELISpot application in causal diagnosis of drug hypersensitivity was based on literature search. The main findings are: (i) ELISpot assay has a good performance in the detection of drug-specific response. (ii) ELISpot results seem to be not substantially impacted by the type of drug or phenotype of the reaction. (iii) Testing within 30 days since the episode of drug hypersensitivity reaction shows a better performance than in later recovery phase. (iv) Data from pediatric population are too scarce to draw any conclusions. (v) Differences in laboratory protocols and in criteria used in the assessment of ELISpot plates along with the issue of the technical feasibility and reproducibility may limit the use of this assay in the routine diagnostic of drug hypersensitivity reactions.
在药物过敏反应患者中,确认因果关系通常有助于决定继续或停止使用特定治疗方法。不幸的是,确定罪魁祸首药物通常很困难。体内方法存在众所周知的缺点,例如皮肤试验的敏感性低或药物激发试验期间复发的风险。因此,实验室检测非常重要,因为它们可以在不使患者面临风险的情况下改善因果诊断。本文在药物过敏反应的背景下综述了酶联免疫斑点(ELISpot)测定法的机制原理和方法学问题。基于文献检索,对 ELISpot 在药物过敏因果诊断中的应用进行了综述。主要发现包括:(i)ELISpot 测定法在检测药物特异性反应方面具有良好的性能。(ii)ELISpot 结果似乎不受药物类型或反应表型的显著影响。(iii)在药物过敏反应发作后 30 天内进行检测比在后期恢复期进行检测具有更好的性能。(iv)来自儿科人群的数据太少,无法得出任何结论。(v)实验室方案和 ELISpot 板评估中使用的标准存在差异,以及技术可行性和可重复性问题可能会限制该测定法在药物过敏反应常规诊断中的应用。