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Characterization of children with recurrent eczema herpeticum and response to treatment with interferon‐gamma

机译:具有复发性湿疹的儿童的表征,以及干扰素-γ治疗的反应

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Abstract Background/Objectives Interferon gamma (IFN‐γ) has been used treat severe atopic dermatitis, with equivocal results. Recurrent eczema herpeticum is an underappreciated, therapeutically challenging complication of severe atopic dermatitis. Defects in IFN‐γ and other cytokine pathways have been identified in individuals with confirmed eczema herpeticum. This suggests possible benefit from IFN‐γ treatment for confirmed eczema herpeticum. The objective of the current study was to evaluate immunologic and microbial parameters and response to IFN‐γ treatment in children with confirmed eczema herpeticum. Methods We performed a retrospective review of medical records from eight children with confirmed eczema herpeticum and two children with severe atopic dermatitis without a history of eczema herpeticum treated with subcutaneous IFN‐γ. Results Our cohort of children with confirmed eczema herpeticum was predominantly male and had high total serum immunoglobulin E, evidence of insufficient toll‐like receptor responses, and streptococcal skin and pharyngeal colonization. The duration of IFN‐γ administration was 4.5‐25?months. Five children had initial control and then relapse. Three had interval flares. Two had no improvement. Injections were well tolerated, without significant adverse effects. Treatment was associated with an increase in total immunoglobulin E. Poor adherence complicated therapy in five patients. All 10 discontinued IFN‐γ for poor perceived efficacy. Conclusion Children with confirmed eczema herpeticum have evidence of impaired innate and adaptive immunity. IFN‐γ did not result in dramatic improvement in either subset. Specific evaluation for IFN‐γ production, function, or receptor defects may help predict response.
机译:摘要背景/目标干扰素γ(IFN-γ)已被使用治疗严重的特征性皮炎,结果效果。复发性湿疹嗜睡是严重的特征性皮炎并发症的低估。在具有证实湿疹的湿疹的个体中鉴定了IFN-γ和其他细胞因子途径的缺陷。这表明来自IFN-γ治疗的可能受益于确诊的湿疹嗜血体。目前研究的目的是评估免疫学和微生物参数,并在具有证实湿疹的儿童中对IFN-γ治疗的反应。方法我们对8名儿童的病历进行了回顾性审查,患有确诊的湿疹的湿疹患有严重的特应性皮炎,没有皮下IFN-γ治疗的湿疹患者。结果我们具有证实湿疹的儿童群体主要是雄性,并且具有高总血清免疫球蛋白E,证据表明无需接受的受体反应,以及链球菌皮肤和咽部殖民化。 IFN-γ给药的持续时间为4.5-25?数月。五个孩子有初始控制,然后复发。三个有间隔耀斑。两个没有改善。注射率良好耐受,无需显着不良反应。治疗与总免疫球蛋白E.较差的粘附复杂治疗增加了5例。所有10都停止了IFN-γ,用于差的感知功效。结论湿疹的儿童具有证实的生先生和适应性免疫的证据。 IFN-γ未导致任一子集的急剧改进。对于IFN-γ生产,功能或受体缺陷的特异性评估可能有助于预测响应。

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