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Non-immediate reactions to β-lactams: Diagnostic value of skin testing and drug provocation test

机译:对β-内酰胺的非直接反应:皮肤测试和药物激发测试的诊断价值

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Background: ?-Lactam (BL) antibiotics can induce non-immediate skin reactions, frequently manifested as exanthema or urticaria. The time between drug intake and the reaction appearance is generally 24-48 h. Because the mechanisms involved are not completely understood, diagnostic tests for these reactions have still to be fully validated. Objective: To evaluate the role of skin and drug provocation tests (DPTs) in the diagnosis of patients with non-immediate reactions to BL. Methods: We evaluated a group of 22 patients who developed maculopapular exanthema or urticarial exanthema after BL intake. Diagnosis was confirmed by DPT with BL. Intradermal/patch testing was performed with benzylpenicilloyl, minor determinant mixture, amoxicillin (AX), ampicillin (AMP) and the culprit drug in patients and in 22 negative controls. Immunohistochemical studies were done in the affected skin at the acute phase of the reaction and after a delayed positive skin test/DPT. IFN-? and IL-4 were quantified in peripheral mononuclear cells, obtained during the positive response to DPT and after resolution of the symptoms. Results: From the total number of cases, 12 patients developed urticarial exanthema and 10 maculopapular exanthema after DPT. Only two of the 22 patients (9%) had a positive delayed intradermal skin test: one to AX/AMP and the other to cloxacillin. Biopsies showed a mononuclear CD4, CD8 infiltrate and activated and memory cells. The cytokine expression showed a Th1 pattern in patients, in contrast with the Th0 pattern in controls. Conclusion: In patients with non-immediate reactions to BLs (maculopapular exathema or urticarial exanthema), the sensitivity of skin testing is low and DPT may be required to establish the diagnosis. The reproducibility of the reactions and the cytokine pattern expressed during the acute episode support a T cell-induced non-immediate response.
机译:背景:β-内酰胺(BL)抗生素可引起非直接的皮肤反应,通常表现为皮疹或荨麻疹。药物摄入和反应出现之间的时间通常为24-48小时。由于尚未完全了解所涉及的机制,因此对于这些反应的诊断测试仍需充分验证。目的:评估皮肤和药物激发试验(DPT)在诊断BL非直接反应患者中的作用。方法:我们评估了22例在BL摄入后发生了斑丘疹性皮疹或荨麻疹性皮疹的患者。 DPT与BL确诊。在患者和22个阴性对照中,使用苄基青霉素,次要决定簇混合物,阿莫西林(AX),氨苄青霉素(AMP)和罪魁祸首药物进行了皮内/斑贴试验。在反应的急性期和延迟的阳性皮肤试验/ DPT后,在受影响的皮肤中进行了免疫组织化学研究。干扰素?在对DPT的阳性反应过程中和症状缓解后获得的外周单个核细胞中对IL-4和IL-4进行了定量。结果:在全部病例中,DPT后有12例患者发生荨麻疹性皮疹,10例发生了斑丘疹性皮疹。 22名患者中只有2名(9%)的皮内延迟皮肤试验阳性:一名为AX / AMP,另一名为氯西林。活检显示单核CD4,CD8浸润,活化和记忆细胞。与对照中的Th0模式相比,患者的细胞因子表达显示出Th1模式。结论:对BLs无立即反应(巨丘疹性皮炎或荨麻疹性皮炎)的患者,皮肤检查的敏感性较低,可能需要DPT来进行诊断。反应的重现性和急性发作期间表达的细胞因子模式支持T细胞诱导的非立即反应。

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